Session | Time | Details |
---|---|---|
09:00 – 10:30 | Coffee and Registration Ground Floor | |
10:30 – 10:40 | Opening remarks on naturalistic imaging Martina Callaghan University College London | |
Naturalistic Neuroscience 1 | 10:40 – 11:30 Keynote | Critical Intelligence: Towards understanding the neural mechanisms of naturalistic adaptive behaviour Dominik Bach University of Bonn More details Less detailsAbstract: All animals including humans have to cope with immediate threat to survive and reproduce. Ample evidence shows that non-human animals behave in sophisticated and apparently goal-directed ways. Rapid decisions between these actions, without much leeway for cognitive or motor errors, poses a formidable computational problem. In my talk, I will give an overview of our research that aims to elucidate the neural mechanisms of these decisions. First, our virtual reality (VR) platform allows simulating immediate threat situations in a safe manner. Second, results from a series of behavioural experiments suggest that human behaviour under threat, while following a standard motor sequence, is flexibly adapted and exhibits many characteristics of reflective planning. Third, we developed a VR head mounted display (HMD) that can be used together with optically pumped magnotmeters. Our data suggest that this HMD allows recording meaningful MEG signals across the entire brain. Together, our results pave the way towards an investigation of naturalistic threat-related decisions with MEG. |
11:30 – 12:00 | Tea break Ground Floor | |
Naturalistic Neuroscience 1 | 12:00 – 12:15 Short talk | Seeing Speech in a New Light: An MEG Study on Augmenting Speech Performance using Rapid Invisible Frequency Tagging (RIFT) Hyojin Park University of Birmingham More details Less details
Co-authors: Yali Pan, Ana Pesquita, Ole Jensen, Katrien Segaert, Hyojin Park
Abstract: In challenging listening environments, visual cues such as lip movements can enhance speech comprehension. Here, we hypothesise that the external modulation of visual speech signals using non-invasive rhythmic stimulation can harnessed to improve speech understanding. We directly tested the hypothesis using a novel paradigm using Rapid Invisible Frequency Tagging (RIFT). RIFT is a technique that modulates visual stimuli at specific frequencies below the threshold of conscious perception to influence neural processing. We manipulated visual speech signals – using RIFT – to influence the integration of visual and auditory information, and measured brain responses using magnetoencephalography (MEG) alongside speech comprehension performance. 40 participants viewed naturalistic speech videos under dichotic listening conditions. One ear was presented with speech that matched the visual speech information (task relevant) while the other was presented with speech that did not (task irrelevant). Both streams of auditory speech were tagged at 40Hz. The visual flicker (55Hz) was implemented on the area whereby participants derive visual speech information: the speaker’s mouth and was modulated by either task relevant or irrelevant speech amplitude envelopes. When modulated by relevant speech information, RIFT significantly enhanced performance in behavioural measures of speech comprehension. The MEG results showed significant effects of auditory and visual tagging in their respective sensory cortices across all experimental conditions. The visual tagging response was significantly stronger when the amplitude was modulated by relevant speech. This stronger tagging response predicted speech comprehension performance. These results suggest that modulating visual input with relevant auditory speech rhythms can facilitate the excitability of visual cortex perhaps leading to enhanced crossmodal integration. Non-invasive sensory stimulation through RIFT may therefore serve as a promising tool for improving speech intelligibility in complex listening environments with multiple competing speakers, particularly for populations such as older adults, individuals with hearing impairments, or those with auditory processing disorders. |
Naturalistic Neuroscience 1 | 12:15 – 12:30 Short talk | Measurement of brain activity during naturalistic tasks Joseph Gibson University of Nottingham More details Less details
Co-authors: Joseph Gibson1, Ryan M. Hill1,2, Niall Holmes1,2, Lukas Rier1,2, Jessikah Fildes1, Matias Ison3, Alan Kirby, Vishal Shah4, Elena Boto2,1, Richard Bowtell1,2, Matthew J. Brookes1,2 1Sir Peter Mansfield Imaging Centre, School of Physics and Astronomy, University of Nottingham, Nottingham, United Kingdom 2Cerca Magnetics Limited, 7-8 Castlebridge Office Village, Kirtley Drive, Nottingham, United Kingdom 3School of Psychology, University of Nottingham, Nottingham, United Kingdom 4QuSpin Inc. 331 South 104th Street, Suite 130, Louisville, Colorado, USA
Abstract: Background: Functional neuroimaging seeks to characterise how neural activity underpins cognition. Most modalities require participants to remain still in enclosed spaces, preventing the implementation of naturalistic tasks that accurately depict real-world environments [1]. Here, we exploited a wearable OPM-MEG system to assess motor network dynamics whilst subjects learnt to play a musical instrument; a complex, naturalistic motor learning task that elicits rich brain activity [2]. Methods: 22 participants were scanned twice using a 192-channel OPM-MEG system [3] while playing ‘Twinkle Twinkle Little Star’ on the violin. Before the first scan, they viewed a video of an expert playing the tune; between scans, they received a 25-minute violin lesson from the same expert. Participants played the tune 30 times in both runs. An IR tracking system (Optitrack, NaturalPoint Inc., Corvallis) was used to monitor participant movement and allowed participants to self-pace the trials. Audio data of each trial were also recorded. OPM-optimised Spatiotemporal Signal Space Separation (tSSS) [4] was used to reduce the effects of motion artefacts. MEG data were source-localised using an LCMV beamformer and beta-band (13-30Hz) dynamics were examined. Results: Large head movements (max (140±100)mm translation / (47±50)° rotation) were observed during the task, however tSSS reduced movement related artefacts (from ~0.9nT to ~0.4pT, shielding factor 2250). The expected movement related beta decrease (MRBD) was observed in all participants during playing of the tune and, compared to rest, localised to the sensorimotor regions. We observed a trend for a greater MRBD (p=0.067) following the lesson compared to before the lesson, in the right dorsolateral motor region. Discussion: We successfully collected a rich naturalistic dataset with 22 participants comprising MEG, audio and motion tracking data. We have shown that despite the presence of large motion we are able to reliably measure high-fidelity MEG data, and we have seen preliminary evidence of differences in motor dynamics following the lesson with an expert. Future analyses will combine measures of trial rating to investigate if brain activity changes with success and explore functional connectivity measures. References: [1] Maselli et al. 2023, 10.1016/j.plrev.2023.07.006 [2] Gelding et al. 2019, 10.1038/s41598-019-53260-9 [3] Schofield et al. 2024, 10.1162/imag_a_00283 [4] Holmes et al. 2024, 10.1109/TBME.2024.3465654 |
Naturalistic Neuroscience 1 | 12:30 – 12:45 Short talk | Auditory evoked responses during ambulatory movement in OP-MEG Stephanie Mellor University of Zurich; ETH Zurich; University College London More details Less details
Co-authors: Tim M. Tierney, James Osborne, Meaghan E. Spedden, Robert A. Seymour, Nicholas A. Alexander, Cody Doyle, David Bobela, George C. O’Neill, Katarzyna Rudzka, Sahitya Puvvada, Maike Schmidt, Vishal Shah, Gareth R. Barnes
Abstract: The latest generation of Optically Pumped Magnetometer (OPM)-based Magnetoencephalography (OP-MEG) systems are increasingly portable and lightweight, making the system easier to wear while undertaking large, whole-body translational and rotational movements. This comes at the expense of added interference due to this movement, and necessitates careful consideration of how non-stationary environmental interference will be addressed. To demonstrate the potential of such setups, we recorded OP-MEG from three participants during auditory stimulation, while the participants walked around a magnetically shielded room, moving across an area of at least 1.7 m2 and rotating by at least 180-degrees. All sensor-specific electronics were housed within a wearable backpack, minimising movement restrictions which would otherwise be imposed by sensor cabling. In this experiment, the maximum peak-to-peak range of the observed magnetic field recorded on a single channel was 25.2 nT, considerably beyond the approximately 4 nT range of many previous OP-MEG systems. We show that adaptive multipole modelling (AMM) with the temporal extension can be used to separate the interference and neuromagnetic signals, despite the large degree of movement and close proximity of the sensor electronics. We observed significant auditory evoked responses at the sensor-level, without the need for source localisation approaches for interference suppression. These findings demonstrate the capability of OP-MEG for conducting naturalistic experiments involving movement. |
Naturalistic Neuroscience 1 | 12:45 – 13:00 Short talk | Neural Dynamics of Free Viewing: Insights from concurrent M/EEG/OPM-MEG and Eye Tracking Matias Ison University of Nottingham More details Less details
Co-authors: Matias J. Ison, Joaquin Gonzalez, Damian Care, Aditi Jain, Ryan Hill, Joseph Gibson, Paul McGraw, Matthew J. Brookes & Juan E. Kamienkowski
Abstract: Eye movements are fundamental to a range of daily activities, from reading to driving. Although behavioural patterns of eye movements during real-world tasks are well-characterised, the neural mechanisms supporting these processes remain elusive, partly due to the substantial artifacts they introduce in M-EEG recordings, often eclipsing neural signals. We present a set of experiments combining eye tracking with EEG, MEG and OPM-MEG recordings in various naturalistic tasks involving eye movements. Participants completed a hybrid visual and memory search task (EEG: N=42; MEG: N=21), in which they searched for one of several items held in memory, and a simulated driving task (OPM-MEG: N=10) using an optically pumped magnetometer system. In the EEG study, we demonstrate how deconvolution methods applied to fixation-related potentials (FRPs) can effectively disentangle temporally overlapping neural events, revealing distinct components related to target detection, task progression, and memory load. MEG source reconstruction of fixation-related activity allowed us to identify a visually evoked lambda response originating in primary visual cortex (V1). Target-related activity was observed in a distributed P3m component and further confirmed with a functional connectivity analysis. Time-frequency analyses revealed neural signatures of memory encoding, retention, and visual search. Applying similar strategies to the driving task enabled to characterization of fixation-aligned visual and attentional processing in dynamic, realistic environments. Altogether, these findings allow us to understand how the neural mechanisms underlying the interaction of memory, attention and visual processing emerge in complex dynamic tasks involving eye movements, offering insights toward more ecologically valid models of cognition. |
13:00 – 14:00 | Lunch Ground Floor | |
Naturalistic Neuroscience 2 | 14:00 – 14:30 Long talk | Catching the young mind in motion: Wearable fNIRS in naturalistic settings Victoria St.Clair, Giulia Serino Birkbeck More details Less detailsAbstract: Young children develop in complex, stimulus-rich environments. Understanding the developing brain in childhood requires conducting naturalistic studies in real-world environments. In this talk, we will discuss various approaches to extending neuroscientific research beyond controlled laboratory settings. Specifically, we will present several naturalistic functional near-infrared spectroscopy (fNIRS) studies conducted at Birkbeck’s ToddlerLab. We will describe a set of hyperscanning studies, in which we use wearable fNIRS with multiple participants simultaneously, to investigate the neural correlates of collaborative problem-solving between preschoolers. We will review the optimisation of our analytical pipelines to reduce the influence of physiological noise in naturalistic signal measurement. We will also discuss how techniques such as diffuse optical tomography (DOT) and virtual reality can be used to simulate everyday experiences within controlled lab environments, particularly in studies involving neurodivergent children. Finally, using attention as a case study, we will present new approaches for exploring naturalistic parent–infant interactions with fNIRS technologies. We will reflect on the lessons learned and the challenges encountered when working with different age groups, populations, and experimental settings. |
Naturalistic Neuroscience 2 | 14:30 – 14:45 Short talk | Decoding real world scenes with mobile EEG and LCD flicker glasses James Dowsett University of Stirling More details Less details
Co-authors: James Dowsett, Inés Martín Muñoz, Paul Taylor
Abstract: We are developing a new method for generating Steady State Visually Evoked Potentials (SSVEPs) of real-world environments in mobile EEG/MEG with LCD flicker glasses (Dowsett et. al. Journal of Neuroscience Methods, 2020). LCD glasses go dark, like sunglasses, when voltage is applied across the glass. The timing can be accurately controlled, allowing the glasses to flicker at any frequency. We previously demonstrated robust SSVEP responses from single channel EEG whilst participants were walking, overcoming the problems of motion artefacts without requiring high numbers of sensors. Using this method, we can apply a high frequency visual flicker to whatever the participant is looking at in the real-world; unlike traditional SSVEP paradigms which are limited to pictures on screens. In the current study we applied this method to decoding real-world environments. Specifically, when participants stood in 6 unique locations and fixated on a point in the distance, while the glasses flickered at 10 Hz, a unique SSVEP waveform shape was generated. We found that SSVEP responses from real world scenes are surprisingly complex and have distinct shapes: they differ markedly across scenes and participants but are consistent within individuals, even across sessions. This unique SSVEP could be reproduced at a later time and also on a separate day, even if various aspects of the visual scene had changed such as overall luminance or cloud cover. The SSVEPs were significantly unique and consistent that the correct scene could be identified with over 90% accuracy. This decoding works with a single electrode, with any of the electrodes tested, and even with a few second’s of data. The decoding was successful with both 10 Hz, 1 Hz and 40 Hz visual flicker; 40 Hz is particularly promising for future research in naturalistic neuroscience as the visual flicker at this frequency is barely noticeable and would not interfere with normal daily activities. We band-pass filtered the SSVEP at various harmonics to investigate the contribution of different frequency bands to decoding accuracy; for all flicker frequencies tested the SSVEP contained information at harmonics of the flicker frequency, and in all cases the gamma band (40 Hz) contained the maximal amount of information about the visual scene. We propose that this is a highly promising method for naturalistic EEG and MEG. |
Naturalistic Neuroscience 2 | 14:45 – 15:00 Short talk | Dynamic functional connectivity during sleep in term and preterm infants Katharine Lee University of Cambridge More details Less details
Co-authors: K. Lee, B. Blanco, R. Cooper, A. Edwards, J. Hebden, K. Pammenter, J. Uchitel, T. Austin
Abstract: Preterm birth has been associated with cognitive, social, and sleep difficulties later in life, outcomes that may be exacerbated by affected sleep (Gao, 2017, Stangenes, 2017). However, the relationship between sleep states, gestational age (GA), and functional brain development remains poorly understood. Studying the role of protected sleep in the NICU may reveal neuroprotective benefits and improve long-term clinical outcomes. High-Density Diffuse Optical Tomography (HD-DOT), a functional near-infrared spectroscopy (fNIRS) technology, has been used to investigate static resting-state functional connectivity (FC) during active sleep (AS) and quiet sleep (QS) states in term-aged infants (Uchitel, 2023). Dynamic FC analysis investigates time-varying patterns in brain activity to shed light on the non-stationary nature of resting state brain functionality. One method proposed for this objective identifies recurring co-activation patterns (CAPs) using clustering algorithms which capture instantaneous brain configurations (Liu, 2018). This study examines dynamic FC in term and preterm infants during sleep to better understand the functional relationship between sleep states and early brain connectivity. HD-DOT data were acquired from sleeping newborns at the Rosie Hospital, Cambridge UK (term cohort: n = 44, GA = 40+0 weeks (median), 38+1 – 42+1 weeks (range); preterm cohort: n = 26, GA = 35+0 weeks (median), 29+1 – 36+6 weeks (range)). Sleep state was labelled as AS/QS using synchronized video or electroencephalography. Frames were sorted by seed activity for three regions of interest (ROI), frontal, central, and parietal regions, and the top 15% frames were selected for k-means clustering. This threshold was chosen because the average of the top 15% of seed-selected frames strongly correlated with the seed-based correlation maps from the static analysis, validating the CAP procedure (see Figure 1). The clustered frames were averaged to create the CAP maps. Dynamic FC was compared across sleep states by calculating CAP consistency, in-participant fraction, dwell time, and transition likelihood for the term cohort. Additionally, regional bilateral activation was compared across sleep states within each CAP using a two proportion Z-test. The post-clustering analysis has been performed for the term cohort and will be applied to the preterm cohort for comparison. |
Naturalistic Neuroscience 2 | 15:00 – 15:15 Short talk | Spike detection in a variety of presentations of epilepsy in children using OPM-MEG Christine Embury Young Epilepsy More details Less details
Co-authors: Christine M Embury, Zelekha Seedat, Kelly St. Pier, Caroline Scott, Friederike Moeller, Krishna Das, Tim Tierney, Gareth Barnes, Matthew Walker, Umesh Vivekananda, J. Helen Cross
Abstract: Epilepsy impacts more than 100k children in the UK alone. Curative treatments in focal lesional epilepsies are largely dependent on precision mapping of epileptogenic activity coupled with structural imaging to determine surgical targets. Previous studies demonstrate the improved mapping of epileptic activity in magnetoencephalography (MEG) relative to electroencephalography (EEG), but these benefits are likely not realised in those ill-suited for the static, one-size-fits-all set-up of traditional cryogenic MEG. The next generation of the technique, optically-pumped magnetometer (OPM)-MEG promises adaptability and improvement in signal detection by bringing the sensors close to the scalp and arranging them flexibly to better fit all head sizes and shapes, particularly advantageous in children. To examine the capabilities of OPM-MEG in detecting epileptic activity in children with epilepsy, we scanned 12 children, six with focal and six with generalised, for 15 minutes to 1 hour while resting or performing tasks. Our OPM-MEG array consisted of 64 QuSpin dual axis sensors (128 channels) housed in child-sized helmets within a light MuRoom coupled with static active shielding (Cerca Magnetics Ltd., Nottingham, England, UK). Data were pre-processed in BESA Research (version 7.1, BESA GmbH, Gräfelfing, Germany) to reduce the influence of cardiac activity. Spikes were marked by experienced clinical scientists. Spike counts were determined per data file and compiled for each participant ranging from 3 detected spikes to more than 70 in the time they were able to complete in the scanner (up to an hour). For those with focal presentations, equivalent current dipoles were mapped on the half-rise of spikes to determine the ability to precisely delineate epileptic foci from interictal activity detected. Overall, we demonstrate the ability of the technique to detect epileptiform activity in children with focal and generalised epilepsies, and with concordance with clinical presentation. This investigation lays the groundwork for a wider use case for the technique, combining the adaptable set-up and increased tolerability with increased sensitivity and precision of the equipment over available clinical tools. OPM-MEG demonstrates an advantageous potential leap for diagnostic capabilities as well as presurgical workup in paediatric epilepsy. |
15:15 – 15:45 | Tea break Ground Floor | |
Naturalistic Neuroscience 2 | 15:45 – 16:00 Short talk | Integrative modeling of beta power responses to speech Christoph Daube University of Glasgow More details Less details
Co-authors: Joachim Gross, Robin A. A. Ince
Abstract: Recently, sensory neuroscience has embraced “naturalistic” experimental conditions in which brain activity is recorded during movie watching, natural scene observation or audiobook listening. In combination with modern video-, image- or audio-processing models, this has yielded unprecedentedly predictive stimulus-computable models of brain activity whose validity is hoped to exceed that of models developed from simplistic artificial stimuli. However, the field is now facing a new set of challenges: With stimulus material full of uncontrolled correlations, it remains unclear what features actually cause response variance. The interpretability is further obscured by the complexity of competitive stimulus processing models. Moreover, linear “encoding models” that relate model representations to brain responses are overly flexible, leaving high degrees of freedom such that many different extracted feature spaces predict response variance to the same degree. It becomes difficult to adjudicate between algorithmically diverse hypotheses. Here, we address these challenges with an approach that aims to generalise the performance of a linear encoding model predicting understudied power time courses as recorded with MEG in response to speech listening. Specifically, we find that such encoding models, trained on passive audiobook listening data, fail to generalise to simple and interpretable but out-of-distribution controlled conditions known from the literature. We diagnose this problem to stem from the largely unconstrained and nonlinear phase responses of the encoding models and devise a regularisation penalty to tackle this. While this effectively reduces the degrees of freedom of the encoding models, some of them achieve competitive performance not only on the passive audiobook listening data, but also on the controlled experiment. However, other models, even when constrained, still fail to generalise to the controlled experiment. This highlights how the consideration of a simplistic but controlled experiment points out dispensable model degrees of freedom and affords an improved and interpretable capacity to adjudicate between models that are equiperformant in the naturalistic condition. Taken together, we subscribe to an integrative perspective on sensory neurosciences that attempts to bridge rich naturalistic datasets to controlled experiments, and specifically considers evidence readily available from existing literature. |
Naturalistic Neuroscience 2 | 16:00 – 16:50 Keynote | Studying the Social Brain using Wearables and Theatre Jamie Ward Goldsmiths More details Less detailsAbstract: Measuring detailed information on how people move, see, and think during realistic social situations can be a powerful method in studying social behaviour and cognition. However, measurement-driven research can be limited by the available technology, with bulky equipment and rigid constraints often confining such work to the laboratory, thus limiting the ecological validity of any findings. In this talk, I will discuss some of the studies on live performance I’ve been involved with, using techniques like wearable EEG hyperscanning, eye-tracking, and motion capture. The work aims to explore the use of live performance and theatre as a laboratory for real-world neuroscience, while developing new measurement techniques using wearable sensors. |
17:00 – 18:00 | Welcome drinks Ground Floor |
09:00 – 10:30
Coffee and Registration
Ground Floor
Ground Floor
10:30 – 10:40
Opening remarks on naturalistic imaging
Martina Callaghan
University College London
Martina Callaghan
University College London
Naturalistic Neuroscience 1
10:40 – 11:30
Keynote
Keynote
Critical Intelligence: Towards understanding the neural mechanisms of naturalistic adaptive behaviour
Dominik Bach
University of Bonn
Abstract:
All animals including humans have to cope with immediate threat to survive and reproduce. Ample evidence shows that non-human animals behave in sophisticated and apparently goal-directed ways. Rapid decisions between these actions, without much leeway for cognitive or motor errors, poses a formidable computational problem. In my talk, I will give an overview of our research that aims to elucidate the neural mechanisms of these decisions. First, our virtual reality (VR) platform allows simulating immediate threat situations in a safe manner. Second, results from a series of behavioural experiments suggest that human behaviour under threat, while following a standard motor sequence, is flexibly adapted and exhibits many characteristics of reflective planning. Third, we developed a VR head mounted display (HMD) that can be used together with optically pumped magnotmeters. Our data suggest that this HMD allows recording meaningful MEG signals across the entire brain. Together, our results pave the way towards an investigation of naturalistic threat-related decisions with MEG.
Dominik Bach
University of Bonn
More details Less details
Abstract:
All animals including humans have to cope with immediate threat to survive and reproduce. Ample evidence shows that non-human animals behave in sophisticated and apparently goal-directed ways. Rapid decisions between these actions, without much leeway for cognitive or motor errors, poses a formidable computational problem. In my talk, I will give an overview of our research that aims to elucidate the neural mechanisms of these decisions. First, our virtual reality (VR) platform allows simulating immediate threat situations in a safe manner. Second, results from a series of behavioural experiments suggest that human behaviour under threat, while following a standard motor sequence, is flexibly adapted and exhibits many characteristics of reflective planning. Third, we developed a VR head mounted display (HMD) that can be used together with optically pumped magnotmeters. Our data suggest that this HMD allows recording meaningful MEG signals across the entire brain. Together, our results pave the way towards an investigation of naturalistic threat-related decisions with MEG.
11:30 – 12:00
Tea break
Ground Floor
Ground Floor
Naturalistic Neuroscience 1
12:00 – 12:15
Short talk
Short talk
Seeing Speech in a New Light: An MEG Study on Augmenting Speech Performance using Rapid Invisible Frequency Tagging (RIFT)
Hyojin Park
University of Birmingham
Hyojin Park
University of Birmingham
More details Less details
Co-authors: Yali Pan, Ana Pesquita, Ole Jensen, Katrien Segaert, Hyojin Park
Abstract:
In challenging listening environments, visual cues such as lip movements can enhance speech comprehension. Here, we hypothesise that the external modulation of visual speech signals using non-invasive rhythmic stimulation can harnessed to improve speech understanding. We directly tested the hypothesis using a novel paradigm using Rapid Invisible Frequency Tagging (RIFT). RIFT is a technique that modulates visual stimuli at specific frequencies below the threshold of conscious perception to influence neural processing. We manipulated visual speech signals – using RIFT – to influence the integration of visual and auditory information, and measured brain responses using magnetoencephalography (MEG) alongside speech comprehension performance. 40 participants viewed naturalistic speech videos under dichotic listening conditions. One ear was presented with speech that matched the visual speech information (task relevant) while the other was presented with speech that did not (task irrelevant). Both streams of auditory speech were tagged at 40Hz. The visual flicker (55Hz) was implemented on the area whereby participants derive visual speech information: the speaker’s mouth and was modulated by either task relevant or irrelevant speech amplitude envelopes. When modulated by relevant speech information, RIFT significantly enhanced performance in behavioural measures of speech comprehension. The MEG results showed significant effects of auditory and visual tagging in their respective sensory cortices across all experimental conditions. The visual tagging response was significantly stronger when the amplitude was modulated by relevant speech. This stronger tagging response predicted speech comprehension performance. These results suggest that modulating visual input with relevant auditory speech rhythms can facilitate the excitability of visual cortex perhaps leading to enhanced crossmodal integration. Non-invasive sensory stimulation through RIFT may therefore serve as a promising tool for improving speech intelligibility in complex listening environments with multiple competing speakers, particularly for populations such as older adults, individuals with hearing impairments, or those with auditory processing disorders.
Abstract:
In challenging listening environments, visual cues such as lip movements can enhance speech comprehension. Here, we hypothesise that the external modulation of visual speech signals using non-invasive rhythmic stimulation can harnessed to improve speech understanding. We directly tested the hypothesis using a novel paradigm using Rapid Invisible Frequency Tagging (RIFT). RIFT is a technique that modulates visual stimuli at specific frequencies below the threshold of conscious perception to influence neural processing. We manipulated visual speech signals – using RIFT – to influence the integration of visual and auditory information, and measured brain responses using magnetoencephalography (MEG) alongside speech comprehension performance. 40 participants viewed naturalistic speech videos under dichotic listening conditions. One ear was presented with speech that matched the visual speech information (task relevant) while the other was presented with speech that did not (task irrelevant). Both streams of auditory speech were tagged at 40Hz. The visual flicker (55Hz) was implemented on the area whereby participants derive visual speech information: the speaker’s mouth and was modulated by either task relevant or irrelevant speech amplitude envelopes. When modulated by relevant speech information, RIFT significantly enhanced performance in behavioural measures of speech comprehension. The MEG results showed significant effects of auditory and visual tagging in their respective sensory cortices across all experimental conditions. The visual tagging response was significantly stronger when the amplitude was modulated by relevant speech. This stronger tagging response predicted speech comprehension performance. These results suggest that modulating visual input with relevant auditory speech rhythms can facilitate the excitability of visual cortex perhaps leading to enhanced crossmodal integration. Non-invasive sensory stimulation through RIFT may therefore serve as a promising tool for improving speech intelligibility in complex listening environments with multiple competing speakers, particularly for populations such as older adults, individuals with hearing impairments, or those with auditory processing disorders.
Naturalistic Neuroscience 1
12:15 – 12:30
Short talk
Short talk
Measurement of brain activity during naturalistic tasks
Joseph Gibson
University of Nottingham
Joseph Gibson
University of Nottingham
More details Less details
Co-authors: Joseph Gibson1, Ryan M. Hill1,2, Niall Holmes1,2, Lukas Rier1,2, Jessikah Fildes1, Matias Ison3, Alan Kirby, Vishal Shah4, Elena Boto2,1, Richard Bowtell1,2, Matthew J. Brookes1,2 1Sir Peter Mansfield Imaging Centre, School of Physics and Astronomy, University of Nottingham, Nottingham, United Kingdom 2Cerca Magnetics Limited, 7-8 Castlebridge Office Village, Kirtley Drive, Nottingham, United Kingdom 3School of Psychology, University of Nottingham, Nottingham, United Kingdom 4QuSpin Inc. 331 South 104th Street, Suite 130, Louisville, Colorado, USA
Abstract:
Background: Functional neuroimaging seeks to characterise how neural activity underpins cognition. Most modalities require participants to remain still in enclosed spaces, preventing the implementation of naturalistic tasks that accurately depict real-world environments [1]. Here, we exploited a wearable OPM-MEG system to assess motor network dynamics whilst subjects learnt to play a musical instrument; a complex, naturalistic motor learning task that elicits rich brain activity [2]. Methods: 22 participants were scanned twice using a 192-channel OPM-MEG system [3] while playing ‘Twinkle Twinkle Little Star’ on the violin. Before the first scan, they viewed a video of an expert playing the tune; between scans, they received a 25-minute violin lesson from the same expert. Participants played the tune 30 times in both runs. An IR tracking system (Optitrack, NaturalPoint Inc., Corvallis) was used to monitor participant movement and allowed participants to self-pace the trials. Audio data of each trial were also recorded. OPM-optimised Spatiotemporal Signal Space Separation (tSSS) [4] was used to reduce the effects of motion artefacts. MEG data were source-localised using an LCMV beamformer and beta-band (13-30Hz) dynamics were examined. Results: Large head movements (max (140±100)mm translation / (47±50)° rotation) were observed during the task, however tSSS reduced movement related artefacts (from ~0.9nT to ~0.4pT, shielding factor 2250). The expected movement related beta decrease (MRBD) was observed in all participants during playing of the tune and, compared to rest, localised to the sensorimotor regions. We observed a trend for a greater MRBD (p=0.067) following the lesson compared to before the lesson, in the right dorsolateral motor region. Discussion: We successfully collected a rich naturalistic dataset with 22 participants comprising MEG, audio and motion tracking data. We have shown that despite the presence of large motion we are able to reliably measure high-fidelity MEG data, and we have seen preliminary evidence of differences in motor dynamics following the lesson with an expert. Future analyses will combine measures of trial rating to investigate if brain activity changes with success and explore functional connectivity measures. References: [1] Maselli et al. 2023, 10.1016/j.plrev.2023.07.006 [2] Gelding et al. 2019, 10.1038/s41598-019-53260-9 [3] Schofield et al. 2024, 10.1162/imag_a_00283 [4] Holmes et al. 2024, 10.1109/TBME.2024.3465654
Abstract:
Background: Functional neuroimaging seeks to characterise how neural activity underpins cognition. Most modalities require participants to remain still in enclosed spaces, preventing the implementation of naturalistic tasks that accurately depict real-world environments [1]. Here, we exploited a wearable OPM-MEG system to assess motor network dynamics whilst subjects learnt to play a musical instrument; a complex, naturalistic motor learning task that elicits rich brain activity [2]. Methods: 22 participants were scanned twice using a 192-channel OPM-MEG system [3] while playing ‘Twinkle Twinkle Little Star’ on the violin. Before the first scan, they viewed a video of an expert playing the tune; between scans, they received a 25-minute violin lesson from the same expert. Participants played the tune 30 times in both runs. An IR tracking system (Optitrack, NaturalPoint Inc., Corvallis) was used to monitor participant movement and allowed participants to self-pace the trials. Audio data of each trial were also recorded. OPM-optimised Spatiotemporal Signal Space Separation (tSSS) [4] was used to reduce the effects of motion artefacts. MEG data were source-localised using an LCMV beamformer and beta-band (13-30Hz) dynamics were examined. Results: Large head movements (max (140±100)mm translation / (47±50)° rotation) were observed during the task, however tSSS reduced movement related artefacts (from ~0.9nT to ~0.4pT, shielding factor 2250). The expected movement related beta decrease (MRBD) was observed in all participants during playing of the tune and, compared to rest, localised to the sensorimotor regions. We observed a trend for a greater MRBD (p=0.067) following the lesson compared to before the lesson, in the right dorsolateral motor region. Discussion: We successfully collected a rich naturalistic dataset with 22 participants comprising MEG, audio and motion tracking data. We have shown that despite the presence of large motion we are able to reliably measure high-fidelity MEG data, and we have seen preliminary evidence of differences in motor dynamics following the lesson with an expert. Future analyses will combine measures of trial rating to investigate if brain activity changes with success and explore functional connectivity measures. References: [1] Maselli et al. 2023, 10.1016/j.plrev.2023.07.006 [2] Gelding et al. 2019, 10.1038/s41598-019-53260-9 [3] Schofield et al. 2024, 10.1162/imag_a_00283 [4] Holmes et al. 2024, 10.1109/TBME.2024.3465654
Naturalistic Neuroscience 1
12:30 – 12:45
Short talk
Short talk
Auditory evoked responses during ambulatory movement in OP-MEG
Stephanie Mellor
University of Zurich; ETH Zurich; University College London
Stephanie Mellor
University of Zurich; ETH Zurich; University College London
More details Less details
Co-authors: Tim M. Tierney, James Osborne, Meaghan E. Spedden, Robert A. Seymour, Nicholas A. Alexander, Cody Doyle, David Bobela, George C. O’Neill, Katarzyna Rudzka, Sahitya Puvvada, Maike Schmidt, Vishal Shah, Gareth R. Barnes
Abstract:
The latest generation of Optically Pumped Magnetometer (OPM)-based Magnetoencephalography (OP-MEG) systems are increasingly portable and lightweight, making the system easier to wear while undertaking large, whole-body translational and rotational movements. This comes at the expense of added interference due to this movement, and necessitates careful consideration of how non-stationary environmental interference will be addressed. To demonstrate the potential of such setups, we recorded OP-MEG from three participants during auditory stimulation, while the participants walked around a magnetically shielded room, moving across an area of at least 1.7 m2 and rotating by at least 180-degrees. All sensor-specific electronics were housed within a wearable backpack, minimising movement restrictions which would otherwise be imposed by sensor cabling. In this experiment, the maximum peak-to-peak range of the observed magnetic field recorded on a single channel was 25.2 nT, considerably beyond the approximately 4 nT range of many previous OP-MEG systems. We show that adaptive multipole modelling (AMM) with the temporal extension can be used to separate the interference and neuromagnetic signals, despite the large degree of movement and close proximity of the sensor electronics. We observed significant auditory evoked responses at the sensor-level, without the need for source localisation approaches for interference suppression. These findings demonstrate the capability of OP-MEG for conducting naturalistic experiments involving movement.
Abstract:
The latest generation of Optically Pumped Magnetometer (OPM)-based Magnetoencephalography (OP-MEG) systems are increasingly portable and lightweight, making the system easier to wear while undertaking large, whole-body translational and rotational movements. This comes at the expense of added interference due to this movement, and necessitates careful consideration of how non-stationary environmental interference will be addressed. To demonstrate the potential of such setups, we recorded OP-MEG from three participants during auditory stimulation, while the participants walked around a magnetically shielded room, moving across an area of at least 1.7 m2 and rotating by at least 180-degrees. All sensor-specific electronics were housed within a wearable backpack, minimising movement restrictions which would otherwise be imposed by sensor cabling. In this experiment, the maximum peak-to-peak range of the observed magnetic field recorded on a single channel was 25.2 nT, considerably beyond the approximately 4 nT range of many previous OP-MEG systems. We show that adaptive multipole modelling (AMM) with the temporal extension can be used to separate the interference and neuromagnetic signals, despite the large degree of movement and close proximity of the sensor electronics. We observed significant auditory evoked responses at the sensor-level, without the need for source localisation approaches for interference suppression. These findings demonstrate the capability of OP-MEG for conducting naturalistic experiments involving movement.
Naturalistic Neuroscience 1
12:45 – 13:00
Short talk
Short talk
Neural Dynamics of Free Viewing: Insights from concurrent M/EEG/OPM-MEG and Eye Tracking
Matias Ison
University of Nottingham
Matias Ison
University of Nottingham
More details Less details
Co-authors: Matias J. Ison, Joaquin Gonzalez, Damian Care, Aditi Jain, Ryan Hill, Joseph Gibson, Paul McGraw, Matthew J. Brookes & Juan E. Kamienkowski
Abstract:
Eye movements are fundamental to a range of daily activities, from reading to driving. Although behavioural patterns of eye movements during real-world tasks are well-characterised, the neural mechanisms supporting these processes remain elusive, partly due to the substantial artifacts they introduce in M-EEG recordings, often eclipsing neural signals. We present a set of experiments combining eye tracking with EEG, MEG and OPM-MEG recordings in various naturalistic tasks involving eye movements. Participants completed a hybrid visual and memory search task (EEG: N=42; MEG: N=21), in which they searched for one of several items held in memory, and a simulated driving task (OPM-MEG: N=10) using an optically pumped magnetometer system. In the EEG study, we demonstrate how deconvolution methods applied to fixation-related potentials (FRPs) can effectively disentangle temporally overlapping neural events, revealing distinct components related to target detection, task progression, and memory load. MEG source reconstruction of fixation-related activity allowed us to identify a visually evoked lambda response originating in primary visual cortex (V1). Target-related activity was observed in a distributed P3m component and further confirmed with a functional connectivity analysis. Time-frequency analyses revealed neural signatures of memory encoding, retention, and visual search. Applying similar strategies to the driving task enabled to characterization of fixation-aligned visual and attentional processing in dynamic, realistic environments. Altogether, these findings allow us to understand how the neural mechanisms underlying the interaction of memory, attention and visual processing emerge in complex dynamic tasks involving eye movements, offering insights toward more ecologically valid models of cognition.
Abstract:
Eye movements are fundamental to a range of daily activities, from reading to driving. Although behavioural patterns of eye movements during real-world tasks are well-characterised, the neural mechanisms supporting these processes remain elusive, partly due to the substantial artifacts they introduce in M-EEG recordings, often eclipsing neural signals. We present a set of experiments combining eye tracking with EEG, MEG and OPM-MEG recordings in various naturalistic tasks involving eye movements. Participants completed a hybrid visual and memory search task (EEG: N=42; MEG: N=21), in which they searched for one of several items held in memory, and a simulated driving task (OPM-MEG: N=10) using an optically pumped magnetometer system. In the EEG study, we demonstrate how deconvolution methods applied to fixation-related potentials (FRPs) can effectively disentangle temporally overlapping neural events, revealing distinct components related to target detection, task progression, and memory load. MEG source reconstruction of fixation-related activity allowed us to identify a visually evoked lambda response originating in primary visual cortex (V1). Target-related activity was observed in a distributed P3m component and further confirmed with a functional connectivity analysis. Time-frequency analyses revealed neural signatures of memory encoding, retention, and visual search. Applying similar strategies to the driving task enabled to characterization of fixation-aligned visual and attentional processing in dynamic, realistic environments. Altogether, these findings allow us to understand how the neural mechanisms underlying the interaction of memory, attention and visual processing emerge in complex dynamic tasks involving eye movements, offering insights toward more ecologically valid models of cognition.
13:00 – 14:00
Lunch
Ground Floor
Ground Floor
Naturalistic Neuroscience 2
14:00 – 14:30
Long talk
Long talk
Catching the young mind in motion: Wearable fNIRS in naturalistic settings
Victoria St.Clair, Giulia Serino
Birkbeck
Abstract:
Young children develop in complex, stimulus-rich environments. Understanding the developing brain in childhood requires conducting naturalistic studies in real-world environments. In this talk, we will discuss various approaches to extending neuroscientific research beyond controlled laboratory settings. Specifically, we will present several naturalistic functional near-infrared spectroscopy (fNIRS) studies conducted at Birkbeck’s ToddlerLab. We will describe a set of hyperscanning studies, in which we use wearable fNIRS with multiple participants simultaneously, to investigate the neural correlates of collaborative problem-solving between preschoolers. We will review the optimisation of our analytical pipelines to reduce the influence of physiological noise in naturalistic signal measurement. We will also discuss how techniques such as diffuse optical tomography (DOT) and virtual reality can be used to simulate everyday experiences within controlled lab environments, particularly in studies involving neurodivergent children. Finally, using attention as a case study, we will present new approaches for exploring naturalistic parent–infant interactions with fNIRS technologies. We will reflect on the lessons learned and the challenges encountered when working with different age groups, populations, and experimental settings.
Victoria St.Clair, Giulia Serino
Birkbeck
More details Less details
Abstract:
Young children develop in complex, stimulus-rich environments. Understanding the developing brain in childhood requires conducting naturalistic studies in real-world environments. In this talk, we will discuss various approaches to extending neuroscientific research beyond controlled laboratory settings. Specifically, we will present several naturalistic functional near-infrared spectroscopy (fNIRS) studies conducted at Birkbeck’s ToddlerLab. We will describe a set of hyperscanning studies, in which we use wearable fNIRS with multiple participants simultaneously, to investigate the neural correlates of collaborative problem-solving between preschoolers. We will review the optimisation of our analytical pipelines to reduce the influence of physiological noise in naturalistic signal measurement. We will also discuss how techniques such as diffuse optical tomography (DOT) and virtual reality can be used to simulate everyday experiences within controlled lab environments, particularly in studies involving neurodivergent children. Finally, using attention as a case study, we will present new approaches for exploring naturalistic parent–infant interactions with fNIRS technologies. We will reflect on the lessons learned and the challenges encountered when working with different age groups, populations, and experimental settings.
Naturalistic Neuroscience 2
14:30 – 14:45
Short talk
Short talk
Decoding real world scenes with mobile EEG and LCD flicker glasses
James Dowsett
University of Stirling
James Dowsett
University of Stirling
More details Less details
Co-authors: James Dowsett, Inés Martín Muñoz, Paul Taylor
Abstract:
We are developing a new method for generating Steady State Visually Evoked Potentials (SSVEPs) of real-world environments in mobile EEG/MEG with LCD flicker glasses (Dowsett et. al. Journal of Neuroscience Methods, 2020). LCD glasses go dark, like sunglasses, when voltage is applied across the glass. The timing can be accurately controlled, allowing the glasses to flicker at any frequency. We previously demonstrated robust SSVEP responses from single channel EEG whilst participants were walking, overcoming the problems of motion artefacts without requiring high numbers of sensors. Using this method, we can apply a high frequency visual flicker to whatever the participant is looking at in the real-world; unlike traditional SSVEP paradigms which are limited to pictures on screens. In the current study we applied this method to decoding real-world environments. Specifically, when participants stood in 6 unique locations and fixated on a point in the distance, while the glasses flickered at 10 Hz, a unique SSVEP waveform shape was generated. We found that SSVEP responses from real world scenes are surprisingly complex and have distinct shapes: they differ markedly across scenes and participants but are consistent within individuals, even across sessions. This unique SSVEP could be reproduced at a later time and also on a separate day, even if various aspects of the visual scene had changed such as overall luminance or cloud cover. The SSVEPs were significantly unique and consistent that the correct scene could be identified with over 90% accuracy. This decoding works with a single electrode, with any of the electrodes tested, and even with a few second’s of data. The decoding was successful with both 10 Hz, 1 Hz and 40 Hz visual flicker; 40 Hz is particularly promising for future research in naturalistic neuroscience as the visual flicker at this frequency is barely noticeable and would not interfere with normal daily activities. We band-pass filtered the SSVEP at various harmonics to investigate the contribution of different frequency bands to decoding accuracy; for all flicker frequencies tested the SSVEP contained information at harmonics of the flicker frequency, and in all cases the gamma band (40 Hz) contained the maximal amount of information about the visual scene. We propose that this is a highly promising method for naturalistic EEG and MEG.
Abstract:
We are developing a new method for generating Steady State Visually Evoked Potentials (SSVEPs) of real-world environments in mobile EEG/MEG with LCD flicker glasses (Dowsett et. al. Journal of Neuroscience Methods, 2020). LCD glasses go dark, like sunglasses, when voltage is applied across the glass. The timing can be accurately controlled, allowing the glasses to flicker at any frequency. We previously demonstrated robust SSVEP responses from single channel EEG whilst participants were walking, overcoming the problems of motion artefacts without requiring high numbers of sensors. Using this method, we can apply a high frequency visual flicker to whatever the participant is looking at in the real-world; unlike traditional SSVEP paradigms which are limited to pictures on screens. In the current study we applied this method to decoding real-world environments. Specifically, when participants stood in 6 unique locations and fixated on a point in the distance, while the glasses flickered at 10 Hz, a unique SSVEP waveform shape was generated. We found that SSVEP responses from real world scenes are surprisingly complex and have distinct shapes: they differ markedly across scenes and participants but are consistent within individuals, even across sessions. This unique SSVEP could be reproduced at a later time and also on a separate day, even if various aspects of the visual scene had changed such as overall luminance or cloud cover. The SSVEPs were significantly unique and consistent that the correct scene could be identified with over 90% accuracy. This decoding works with a single electrode, with any of the electrodes tested, and even with a few second’s of data. The decoding was successful with both 10 Hz, 1 Hz and 40 Hz visual flicker; 40 Hz is particularly promising for future research in naturalistic neuroscience as the visual flicker at this frequency is barely noticeable and would not interfere with normal daily activities. We band-pass filtered the SSVEP at various harmonics to investigate the contribution of different frequency bands to decoding accuracy; for all flicker frequencies tested the SSVEP contained information at harmonics of the flicker frequency, and in all cases the gamma band (40 Hz) contained the maximal amount of information about the visual scene. We propose that this is a highly promising method for naturalistic EEG and MEG.
Naturalistic Neuroscience 2
14:45 – 15:00
Short talk
Short talk
Dynamic functional connectivity during sleep in term and preterm infants
Katharine Lee
University of Cambridge
Katharine Lee
University of Cambridge
More details Less details
Co-authors: K. Lee, B. Blanco, R. Cooper, A. Edwards, J. Hebden, K. Pammenter, J. Uchitel, T. Austin
Abstract:
Preterm birth has been associated with cognitive, social, and sleep difficulties later in life, outcomes that may be exacerbated by affected sleep (Gao, 2017, Stangenes, 2017). However, the relationship between sleep states, gestational age (GA), and functional brain development remains poorly understood. Studying the role of protected sleep in the NICU may reveal neuroprotective benefits and improve long-term clinical outcomes. High-Density Diffuse Optical Tomography (HD-DOT), a functional near-infrared spectroscopy (fNIRS) technology, has been used to investigate static resting-state functional connectivity (FC) during active sleep (AS) and quiet sleep (QS) states in term-aged infants (Uchitel, 2023). Dynamic FC analysis investigates time-varying patterns in brain activity to shed light on the non-stationary nature of resting state brain functionality. One method proposed for this objective identifies recurring co-activation patterns (CAPs) using clustering algorithms which capture instantaneous brain configurations (Liu, 2018). This study examines dynamic FC in term and preterm infants during sleep to better understand the functional relationship between sleep states and early brain connectivity. HD-DOT data were acquired from sleeping newborns at the Rosie Hospital, Cambridge UK (term cohort: n = 44, GA = 40+0 weeks (median), 38+1 – 42+1 weeks (range); preterm cohort: n = 26, GA = 35+0 weeks (median), 29+1 – 36+6 weeks (range)). Sleep state was labelled as AS/QS using synchronized video or electroencephalography. Frames were sorted by seed activity for three regions of interest (ROI), frontal, central, and parietal regions, and the top 15% frames were selected for k-means clustering. This threshold was chosen because the average of the top 15% of seed-selected frames strongly correlated with the seed-based correlation maps from the static analysis, validating the CAP procedure (see Figure 1). The clustered frames were averaged to create the CAP maps. Dynamic FC was compared across sleep states by calculating CAP consistency, in-participant fraction, dwell time, and transition likelihood for the term cohort. Additionally, regional bilateral activation was compared across sleep states within each CAP using a two proportion Z-test. The post-clustering analysis has been performed for the term cohort and will be applied to the preterm cohort for comparison.
Abstract:
Preterm birth has been associated with cognitive, social, and sleep difficulties later in life, outcomes that may be exacerbated by affected sleep (Gao, 2017, Stangenes, 2017). However, the relationship between sleep states, gestational age (GA), and functional brain development remains poorly understood. Studying the role of protected sleep in the NICU may reveal neuroprotective benefits and improve long-term clinical outcomes. High-Density Diffuse Optical Tomography (HD-DOT), a functional near-infrared spectroscopy (fNIRS) technology, has been used to investigate static resting-state functional connectivity (FC) during active sleep (AS) and quiet sleep (QS) states in term-aged infants (Uchitel, 2023). Dynamic FC analysis investigates time-varying patterns in brain activity to shed light on the non-stationary nature of resting state brain functionality. One method proposed for this objective identifies recurring co-activation patterns (CAPs) using clustering algorithms which capture instantaneous brain configurations (Liu, 2018). This study examines dynamic FC in term and preterm infants during sleep to better understand the functional relationship between sleep states and early brain connectivity. HD-DOT data were acquired from sleeping newborns at the Rosie Hospital, Cambridge UK (term cohort: n = 44, GA = 40+0 weeks (median), 38+1 – 42+1 weeks (range); preterm cohort: n = 26, GA = 35+0 weeks (median), 29+1 – 36+6 weeks (range)). Sleep state was labelled as AS/QS using synchronized video or electroencephalography. Frames were sorted by seed activity for three regions of interest (ROI), frontal, central, and parietal regions, and the top 15% frames were selected for k-means clustering. This threshold was chosen because the average of the top 15% of seed-selected frames strongly correlated with the seed-based correlation maps from the static analysis, validating the CAP procedure (see Figure 1). The clustered frames were averaged to create the CAP maps. Dynamic FC was compared across sleep states by calculating CAP consistency, in-participant fraction, dwell time, and transition likelihood for the term cohort. Additionally, regional bilateral activation was compared across sleep states within each CAP using a two proportion Z-test. The post-clustering analysis has been performed for the term cohort and will be applied to the preterm cohort for comparison.
Naturalistic Neuroscience 2
15:00 – 15:15
Short talk
Short talk
Spike detection in a variety of presentations of epilepsy in children using OPM-MEG
Christine Embury
Young Epilepsy
Christine Embury
Young Epilepsy
More details Less details
Co-authors: Christine M Embury, Zelekha Seedat, Kelly St. Pier, Caroline Scott, Friederike Moeller, Krishna Das, Tim Tierney, Gareth Barnes, Matthew Walker, Umesh Vivekananda, J. Helen Cross
Abstract:
Epilepsy impacts more than 100k children in the UK alone. Curative treatments in focal lesional epilepsies are largely dependent on precision mapping of epileptogenic activity coupled with structural imaging to determine surgical targets. Previous studies demonstrate the improved mapping of epileptic activity in magnetoencephalography (MEG) relative to electroencephalography (EEG), but these benefits are likely not realised in those ill-suited for the static, one-size-fits-all set-up of traditional cryogenic MEG. The next generation of the technique, optically-pumped magnetometer (OPM)-MEG promises adaptability and improvement in signal detection by bringing the sensors close to the scalp and arranging them flexibly to better fit all head sizes and shapes, particularly advantageous in children. To examine the capabilities of OPM-MEG in detecting epileptic activity in children with epilepsy, we scanned 12 children, six with focal and six with generalised, for 15 minutes to 1 hour while resting or performing tasks. Our OPM-MEG array consisted of 64 QuSpin dual axis sensors (128 channels) housed in child-sized helmets within a light MuRoom coupled with static active shielding (Cerca Magnetics Ltd., Nottingham, England, UK). Data were pre-processed in BESA Research (version 7.1, BESA GmbH, Gräfelfing, Germany) to reduce the influence of cardiac activity. Spikes were marked by experienced clinical scientists. Spike counts were determined per data file and compiled for each participant ranging from 3 detected spikes to more than 70 in the time they were able to complete in the scanner (up to an hour). For those with focal presentations, equivalent current dipoles were mapped on the half-rise of spikes to determine the ability to precisely delineate epileptic foci from interictal activity detected. Overall, we demonstrate the ability of the technique to detect epileptiform activity in children with focal and generalised epilepsies, and with concordance with clinical presentation. This investigation lays the groundwork for a wider use case for the technique, combining the adaptable set-up and increased tolerability with increased sensitivity and precision of the equipment over available clinical tools. OPM-MEG demonstrates an advantageous potential leap for diagnostic capabilities as well as presurgical workup in paediatric epilepsy.
Abstract:
Epilepsy impacts more than 100k children in the UK alone. Curative treatments in focal lesional epilepsies are largely dependent on precision mapping of epileptogenic activity coupled with structural imaging to determine surgical targets. Previous studies demonstrate the improved mapping of epileptic activity in magnetoencephalography (MEG) relative to electroencephalography (EEG), but these benefits are likely not realised in those ill-suited for the static, one-size-fits-all set-up of traditional cryogenic MEG. The next generation of the technique, optically-pumped magnetometer (OPM)-MEG promises adaptability and improvement in signal detection by bringing the sensors close to the scalp and arranging them flexibly to better fit all head sizes and shapes, particularly advantageous in children. To examine the capabilities of OPM-MEG in detecting epileptic activity in children with epilepsy, we scanned 12 children, six with focal and six with generalised, for 15 minutes to 1 hour while resting or performing tasks. Our OPM-MEG array consisted of 64 QuSpin dual axis sensors (128 channels) housed in child-sized helmets within a light MuRoom coupled with static active shielding (Cerca Magnetics Ltd., Nottingham, England, UK). Data were pre-processed in BESA Research (version 7.1, BESA GmbH, Gräfelfing, Germany) to reduce the influence of cardiac activity. Spikes were marked by experienced clinical scientists. Spike counts were determined per data file and compiled for each participant ranging from 3 detected spikes to more than 70 in the time they were able to complete in the scanner (up to an hour). For those with focal presentations, equivalent current dipoles were mapped on the half-rise of spikes to determine the ability to precisely delineate epileptic foci from interictal activity detected. Overall, we demonstrate the ability of the technique to detect epileptiform activity in children with focal and generalised epilepsies, and with concordance with clinical presentation. This investigation lays the groundwork for a wider use case for the technique, combining the adaptable set-up and increased tolerability with increased sensitivity and precision of the equipment over available clinical tools. OPM-MEG demonstrates an advantageous potential leap for diagnostic capabilities as well as presurgical workup in paediatric epilepsy.
15:15 – 15:45
Tea break
Ground Floor
Ground Floor
Naturalistic Neuroscience 2
15:45 – 16:00
Short talk
Short talk
Integrative modeling of beta power responses to speech
Christoph Daube
University of Glasgow
Christoph Daube
University of Glasgow
More details Less details
Co-authors: Joachim Gross, Robin A. A. Ince
Abstract:
Recently, sensory neuroscience has embraced “naturalistic” experimental conditions in which brain activity is recorded during movie watching, natural scene observation or audiobook listening. In combination with modern video-, image- or audio-processing models, this has yielded unprecedentedly predictive stimulus-computable models of brain activity whose validity is hoped to exceed that of models developed from simplistic artificial stimuli. However, the field is now facing a new set of challenges: With stimulus material full of uncontrolled correlations, it remains unclear what features actually cause response variance. The interpretability is further obscured by the complexity of competitive stimulus processing models. Moreover, linear “encoding models” that relate model representations to brain responses are overly flexible, leaving high degrees of freedom such that many different extracted feature spaces predict response variance to the same degree. It becomes difficult to adjudicate between algorithmically diverse hypotheses. Here, we address these challenges with an approach that aims to generalise the performance of a linear encoding model predicting understudied power time courses as recorded with MEG in response to speech listening. Specifically, we find that such encoding models, trained on passive audiobook listening data, fail to generalise to simple and interpretable but out-of-distribution controlled conditions known from the literature. We diagnose this problem to stem from the largely unconstrained and nonlinear phase responses of the encoding models and devise a regularisation penalty to tackle this. While this effectively reduces the degrees of freedom of the encoding models, some of them achieve competitive performance not only on the passive audiobook listening data, but also on the controlled experiment. However, other models, even when constrained, still fail to generalise to the controlled experiment. This highlights how the consideration of a simplistic but controlled experiment points out dispensable model degrees of freedom and affords an improved and interpretable capacity to adjudicate between models that are equiperformant in the naturalistic condition. Taken together, we subscribe to an integrative perspective on sensory neurosciences that attempts to bridge rich naturalistic datasets to controlled experiments, and specifically considers evidence readily available from existing literature.
Abstract:
Recently, sensory neuroscience has embraced “naturalistic” experimental conditions in which brain activity is recorded during movie watching, natural scene observation or audiobook listening. In combination with modern video-, image- or audio-processing models, this has yielded unprecedentedly predictive stimulus-computable models of brain activity whose validity is hoped to exceed that of models developed from simplistic artificial stimuli. However, the field is now facing a new set of challenges: With stimulus material full of uncontrolled correlations, it remains unclear what features actually cause response variance. The interpretability is further obscured by the complexity of competitive stimulus processing models. Moreover, linear “encoding models” that relate model representations to brain responses are overly flexible, leaving high degrees of freedom such that many different extracted feature spaces predict response variance to the same degree. It becomes difficult to adjudicate between algorithmically diverse hypotheses. Here, we address these challenges with an approach that aims to generalise the performance of a linear encoding model predicting understudied power time courses as recorded with MEG in response to speech listening. Specifically, we find that such encoding models, trained on passive audiobook listening data, fail to generalise to simple and interpretable but out-of-distribution controlled conditions known from the literature. We diagnose this problem to stem from the largely unconstrained and nonlinear phase responses of the encoding models and devise a regularisation penalty to tackle this. While this effectively reduces the degrees of freedom of the encoding models, some of them achieve competitive performance not only on the passive audiobook listening data, but also on the controlled experiment. However, other models, even when constrained, still fail to generalise to the controlled experiment. This highlights how the consideration of a simplistic but controlled experiment points out dispensable model degrees of freedom and affords an improved and interpretable capacity to adjudicate between models that are equiperformant in the naturalistic condition. Taken together, we subscribe to an integrative perspective on sensory neurosciences that attempts to bridge rich naturalistic datasets to controlled experiments, and specifically considers evidence readily available from existing literature.
Naturalistic Neuroscience 2
16:00 – 16:50
Keynote
Keynote
Studying the Social Brain using Wearables and Theatre
Jamie Ward
Goldsmiths
Abstract:
Measuring detailed information on how people move, see, and think during realistic social situations can be a powerful method in studying social behaviour and cognition. However, measurement-driven research can be limited by the available technology, with bulky equipment and rigid constraints often confining such work to the laboratory, thus limiting the ecological validity of any findings. In this talk, I will discuss some of the studies on live performance I’ve been involved with, using techniques like wearable EEG hyperscanning, eye-tracking, and motion capture. The work aims to explore the use of live performance and theatre as a laboratory for real-world neuroscience, while developing new measurement techniques using wearable sensors.
Jamie Ward
Goldsmiths
More details Less details
Abstract:
Measuring detailed information on how people move, see, and think during realistic social situations can be a powerful method in studying social behaviour and cognition. However, measurement-driven research can be limited by the available technology, with bulky equipment and rigid constraints often confining such work to the laboratory, thus limiting the ecological validity of any findings. In this talk, I will discuss some of the studies on live performance I’ve been involved with, using techniques like wearable EEG hyperscanning, eye-tracking, and motion capture. The work aims to explore the use of live performance and theatre as a laboratory for real-world neuroscience, while developing new measurement techniques using wearable sensors.
17:00 – 18:00
Welcome drinks
Ground Floor
Ground Floor
Session | Time | Details |
---|---|---|
09:00 – 09:20 | Coffee and Registration Ground Floor | |
09:20 – 09:50 | Coffee Break; Business meeting Ground Floor; Dickins Library | |
09:50 – 10:00 | Opening remarks Yulia Bezsudnova, Gareth Barnes University College London | |
Dementia Research | 10:00 – 10:30 Long talk | Clinical Utility of MEG in Dementia Care: Insights from Outpatient Experience Yoshihito Shigihara Hokuto Hospital More details Less details
Co-authors: Hideyuki Hoshi, Momoko Kobayashi, Keisuke Fukasawa, Keita Shibamiya, Sayuri Ichikawa, Yoko Hirata
Abstract: Dementia is a functionally defined condition in which various brain diseases lead to cognitive impairments that interfere with daily living. The severity of these impairments does not always correspond directly to the severity of the underlying disease, as multiple factors—such as lifestyle—modulate this relationship. Clinically, we often observe that patients show cognitive improvements after receiving well-being advice from clinicians, even when the causative disease is progressive. This highlights the need for effective tools to monitor treatment outcomes. While neuropsychological assessments are valuable, they have inherent limitations, such as learning and ceiling effects. Magnetoencephalography (MEG) offers complementary insights by capturing brain activity associated with cognitive states, particularly during the rest. Resting-state MEG provides rich information that can be used to infer both functional and pathological brain changes. Since 2019, we have routinely used MEG in our outpatient department for the assessment and treatment of dementia, accumulating experience with over 500 patients reporting subjective and/or objective cognitive impairments. Our findings include: 1. Different spectral parameters of MEG data are associated with distinct aspects of cognitive function. 2. These parameters also correlate with cerebral blood flow (assessed via ultrasonography) and pathological changes (measured using single-photon emission computed tomography). 3. Nonpharmacological treatments improve patients’ cognitive states, and these improvements are reflected in changes in MEG-recorded brain activity. 4. Clinical staff’s subjective impressions of cognitive improvement align more closely with changes in MEG data than with neuropsychological test scores. 5. MEG can predict cognitive improvement following nonpharmacological interventions. In this presentation, we summarise these findings and discuss the future role of MEG in clinical practice, with the goal of enhancing patient well-being. We propose that ‘MEG’ stands for ‘Make Everyone Good’, reflecting its potential to support a more holistic and human-centred approach to dementia care. |
Dementia Research | 10:30 – 10:45 Short talk | MEG network dynamics offer enhanced sensitivity for detecting amyloid pathology and disease progression in Alzheimer’s disease Mats van Es University of Oxford More details Less details
Co-authors: Mats W.J. van Es, Andrew J. Quinn, Jemma Pitt, Tony Thayanandan, Marlou N Perquin, Alexandra Krugliak, Ece Kocagoncu, Juliette Lanskey, Chetan Gohil, Vanessa Raymont, James B. Rowe, Anna C. Nobre, Mark W. Woolrich
Abstract: Current diagnosis and monitoring of Alzheimer’s Disease (AD) focus on Amyloid-beta, Tau aggregates, and atrophy. To advance treatments, new biomarkers are needed that are sensitive, reliable, and predictive of disease progression. We evaluated MEG spectral density in early symptomatic AD. We used data from the New Therapeutics in Alzheimer’s Disease (NTAD) study [Lanskey et al., 2022]: participants aged 50-85 with mild cognitive impairment or early AD (n=67, biomarker positive) and normal cognition (n=34, biomarker negative). Independent Cam-CAN data (N=612) were used to model confounds, including age, sex, and scanner effects. We examined spectral activity during resting wakefulness. First, we assessed static spectral power to replicate previous findings. Next, we applied Hidden-Markov Modelling (HMM) [Vidaurre et al., 2018] with 10 states to investigate brain network dynamics as a potentially more sensitive biomarker. We assessed cross-sectional differences (amyloid groups) and longitudinal changes (baseline to annual follow-up in amyloid-positive participants), and evaluated two-week test-retest reliability using intraclass correlation coefficient (ICC). We replicated previous findings of oscillatory slowing in AD: increased delta/theta and decreased alpha/beta power. These effects were robust at the group level but small to moderate in size (Cohen’s f2 < 0.35). Similar trends appeared in brain network spectra, with sensitivity varying by network and frequency band. Effect sizes exceeded those of static spectra in 6/10 states, and were strongest in a parietal alpha network (Cohen’s f2 > 0.7) in the alpha/beta band. Excluding one network, power in all networks was reliable (ICC > 0.8) and more reliable than static features. Longitudinally, the most pronounced changes occurred in a distinct network and frequency band compared to cross-sectional differences: patients showed reduced high gamma power (44-120 Hz) in a frontal network (Cohen’s f2 > 1.0), an effect only hinted at in static spectra. These results indicate that brain network dynamics are sensitive to amyloid status and disease progression, and that network spectra are more sensitive and reliable than static spectra. This suggests promise as a biomarker tool. Future analyses will examine correlations with cognitive scores and other biomarkers. |
Dementia Research | 10:45 – 11:00 Short talk | Practice-induced reductions in Gamma power in Response to Proper Name Anomia Therapy in people with dementia: An MEG Study Aygun Badalova University College London More details Less details
Co-authors: Aygun Badalova 1,3 Tae Twomey 1,3, Vladimir Litvak 4 George O’Neill 4 Alex Leff 1,2,3
Abstract: Objective Proper name anomia is a common language deficit observed in people with dementia (PWD), impacting their ability to recall and retrieve the names of familiar people. This study investigates the neural changes associated with a 6-week, app-based, proper-name anomia therapy in PWD using MEG and whether this learning-based therapy leads to changes in gamma-band oscillatory activity within the left superior temporal gyrus (STG).The left STG was chosen for its key role in language processing and name retrieval. Methods 26 PWD with proper name anomia were recruited. Following baseline assessment, patients underwent a structured 6-week proper-name anomia therapy program using a novel app called Gotcha! Participants were trained to name 6-10 faces (usually their relatives and close friends), using confrontation naming and audio cueing methods. MEG recordings were obtained at two time points: pre- and post-therapy while PWD were presented with pictures of the trained familiar or untrained, but famous faces, which they named aloud. MEG data were analysed in SPM, we measured source localised gamma-band (30-80 Hz) power 0-3400 ms after the onset of a face We ran a 2×2 factorial analysis on our source images (famous v familiar; pre- v post-therapy) using a repeated-measures ANOVA to look for changes in power across conditions. The behavioural data was analysed using a repeated-measures ANOVA with the outcome being correctly named faces while free-naming. Results Behavioural data analysis revealed that the Gotcha! therapy app is effective with a significant effect at the group level of training > baseline, F(1,36)=55.47, p=0.01. For the MEG analysis, we identified a large cluster of 1205 voxels situated in the left superior temporal gyrus (MNI: -54 10 -6, F=11.92, p=0.016 peak level FWE-corrected over the left STG) where gamma reduction was associated with training (pre-post) of familiar faces, but not (untrained) famous faces. This is the first study to demonstrate that this region also supports re-learning for familiar face-name associations in PWD. Discussion App-based proper name anomia retraining appears to be an effective therapy for PWD. Initial MEG findings suggest that therapy effects are manifest in areas associated with face-naming. |
Dementia Research | 11:00 – 11:15 Short talk | Electrophysiological correlates of the Last-In-First-Out hypothesis of age-related white matter decline. Atheer Al-Manea University of Birmingham More details Less details
Co-authors: Magda Chechlacz & Andrew J Quinn
Abstract: The Last-In-First-Out (LIFO) hypothesis proposes that phylogenetically newer, later-myelinating brain regions are more vulnerable to age-related degeneration than evolutionarily older structures. However, the electrophysiological correlates of this structural aging pattern remain poorly understood. We will test whether peak alpha frequency and power decline are more impacted by variability in anterior or posterior tracts of the corpus callosum. The alpha rhythm is spatially localized closer to the posterior tracts whereas the LIFO hypothesis suggests that the anterior tracts are more susceptible to age related deterioration. We combined high-resolution diffusion MRI tractography, SIFT2 streamline weighting, and volumetric analyses in 542 adults (18–88 y) from the Cam-CAN ageing cohort, using the multimodal micapipe (v0.2.3) pipeline, to chart age-related white matter decline across three corpus callosum (CC) segments: Forceps Minor (FMI), mid-body (CC_MID), and Forceps Major (FMA). Segmentation of these anterior, middle, and posterior callosal bundles revealed a pronounced anterior-to-posterior gradient of deterioration. The Forceps Minor exhibited the most substantial decline in both volume and weighted fractional anisotropy (FA), while mid-body demonstrated intermediate vulnerability, and Forceps Major showed relative preservation. Standard diffusion tensor-imaging (DTI) metrics (mean FA) failed to detect subtle mid-body and posterior declines whereas SIFT2-weighted FA revealed robust negative age slopes. Volumes declined steeply in all segments, and quadratic models further revealed accelerated deterioration in later decades. This replicated the pattern of structural connectivity suggested by the LIFO hypothesis. A GLM-Spectrum analysis predicting individual variability in the resting state power spectrum shows the strongest effects with the anterior corpus callosum compared to the middle, or posterior tracts. This structure-function dissociation refines the LIFO model by integrating advanced tractography and electrophysiological metrics to capture divergent aging trajectories in the human brain’s structure and function. |
11:15 – 11:45 | Tea break Ground Floor | |
Dynamics | 11:45 – 12:00 Short talk | Distinct spectral profiles of ageing and neurodegeneration Andrew Quinn University of Birmingham More details Less details
Co-authors: Andrew J. Quinn, Mats W.J. van Es, Jemma Pitt, Tony Thayanandan, Marlou N Perquin, Alexandra Krugliak, Ece Kocagoncu, Juliette Lanskey, Chetan Gohil, Vanessa Raymont, James B. Rowe, Anna C. Nobre, Mark W. Woolrich
Abstract: Non-invasive recordings of brain electrophysiology offer insight into age-related decline and disease related degeneration of neuronal function. These changes are reflected by alterations in the power spectrum of EEG and MEG recordings. Statistically rigorous analysis methodologies are needed to translate these findings into clinically meaningful metrics that address the global challenge of maintaining brain health in ageing populations. We us the CamCAN dataset to identify a full-frequency profile of the ageing effect on resting state electrophysiology and establish a basis for effect size calculation on the spectrum. Specific oscillations within this profile have different effect sizes indicating that sample size planning for ageing effects must consider the specific features of interest. The frequency profile of ageing is strongly robust to a range of common covariates and partially robust to modelling of grey matter volume. We establish that a well powered sample may become underpowered when analyses look to establish the age effect that is linearly separable from an age-relevant covariate such as grey matter volume. These results help to consolidate a variable literature of age effects on resting state brain electrophysiology and provide a pathway towards formal comparison and assessment of candidate markers for brain health in ageing. These results are used as the basis to explore the distinction between Alzheimer’s Disease (AD) and healthy ageing, and specifically whether neurodegeneration can be considered a form of accelerated brain ageing. We used data from the New Therapeutics in Alzheimer’s Disease (NTAD) study to compute full-frequency profiles of ageing and of presence of Alzheimer’s pathology. The results show distinct spectral profiles for each predictor indicating that although age is a strong risk factor for neurodegeneration it has a separate impact on neuronal function. Crucially, the full spectral profiles showed a distinction between ageing and neurodegeneration, they can have highly correlated spatial effects at individual frequencies. Specifically, both ageing and the presence of AD lead to a decrease in posterior spectral power in the high alpha range, whereas they have distinct effects in the beta range. This result suggests that both high sensitivity for AD pathology and separability close covariates must both be optimised when searching for clinical markers. |
Dynamics | 12:00 – 12:15 Short talk | Universal rhythmic architecture uncovers distinct modes of neural dynamics Ayelet Landau University College London More details Less details
Co-authors: Golan Karvat, Maité Crespo-García, Gal Vishne, Michael C Anderson
Abstract: A prominent idea in neuroscience, for over a century, has been that brain activity comprises electrical field potentials that oscillate in different frequency bands. This notion, however, has been critiqued on various grounds. Most recently, evidence suggests that brain oscillations may sometimes appear as transient bursts rather than continuous rhythms. Here, we explore the hypothesis that rhythmicity—whether sustained or bursty—represents an additional organizing principle or dimension of brain function. We analysed neurophysiological spectra of 859 participants covering diverse species, recording methods, ages (18-88), brain regions, and cognitive states in both healthy and disease, using a new rhythmicity measure. Through computer simulations and brain stimulation, we identified a universal spectral architecture comprising two categories: high-rhythmicity bands linked to continuous oscillations and new low-rhythmicity bands characterized by brief bursts. Beyond characterizing this architecture I will discuss its functional consequences and examine whether the two categories of activity relate to two different modes of information processing. Namely, sustained bands reflecting maintenance of ongoing activity, and transient bands indicating responses to changes. |
Dynamics | 12:15 – 12:30 Short talk | The temporal dynamics of speech motor control during imagined speech Francesco Mantegna University of Oxford More details Less details
Co-authors: Joan Orpella, David Poeppel
Abstract: Speech production constitutes a fundamental activity inherent in our interactions and communication with others. The apparent ease we experience during speech production conceals the inherent complexity of its underlying machinery. The subjective feeling that speech production is seamless derives from extensive prior experience, which we constantly deploy to make predictions and apply corrections as we speak. One convenient way to study these feedforward and feedback control mechanisms is through imagined speech—that is, the internal generation of speech in the absence of motor articulation and its sensory consequences. When speech is conjured up internally, control mechanisms are not overshadowed by brain activity associated with motor execution and sensory feedback, making them more easily identifiable in the brain signal. During my PhD, I conducted three magnetoencephalography (MEG) studies investigating the temporal dynamics of speech motor control during imagined speech. The first study (1) explores how the decodability of sensory and motor transient neural representations associated with imagined speech varies depending on speech content (e.g., consonants vs. vowels). The second study (2) reveals a dynamic shift in the hemispheric lateralization of functional connectivity between motor and auditory areas, suggesting that feedforward control exhibits left lateralization prior to imagined speech production, while feedback control exhibits right lateralization afterward. The third study (3) demonstrates a spatiotemporal segregation of frequency-specific power modulations in the alpha and beta frequency bands in motor and auditory areas, respectively. Additional analyses confirmed that these two frequencies are not harmonics but rather spectrally distinct: a somatomotor ‘mu’ rhythm and an auditory ‘tau’ rhythm. This segregation indicates distinct coding schemes that necessitate sensorimotor coordination during imagined speech. Collectively, these studies contribute to advancing our understanding of speech motor control, offering a more precise temporal characterization of both covert and overt speech production subprocesses and thereby shedding new light on its neural architecture. Moreover, they lay the foundation for a non-invasive brain-computer interface, a topic that I am currently investigating in my postdoc. |
12:30 – 13:00 Flash talks | Session 1 flash talks Mary Ward Hall | |
13:00 – 14:30 | Lunch and poster session 1 Ground Floor | |
Cognitive Neuroscience | 14:30 – 15:00 Long talk | Working Memory Reactivation Across Embedded Language Structures Jiaqi Li University of Oxford More details Less details
Co-authors: Jiaqi Li, Yali Pan, Hyojin Park, Peter Hagoort, Huan Luo, Ole Jensen
Abstract: Recursiveness, involving hierarchical embedding of clauses, is a key feature of human language that depends on working memory (WM). During speech comprehension, listeners must maintain previously processed words or phrases for later unification. However, the neural mechanisms underlying how WM supports the processing of complex recursive structures remain unclear. We constructed English sentences with embedded language structures (e.g. The dog, who chases the cat, jumps over the mud.) and recorded magnetoencephalography (MEG) signals while English native speakers listened to these sentences. Neural decoding results demonstrate that during speech comprehension, previously encoded information (e.g. the dog) is maintained in an activity-silent state until syntactic cues (e.g. jumps over) trigger unification. In our study, the verb (e.g. jumps over) reactivated the subject constituent that preceded the embedded clause (e.g. the dog) after 600 ms of the verb’s onset. Furthermore, source-level searchlight analysis reveals that the memory reactivation first occurs in the prefrontal cortex followed by reactivation in the temporal cortex. Further analysis revealed that the syntactic structure of the embedded clause specifically modulated the memory performance related to unification and the strength of memory reactivation. This study provides crucial insights into the temporal and spatial dynamics of WM functions required for unification operations across embedded structures. By bridging the gap between the domains of WM and language comprehension, this work offers a novel perspective with potential implications for refining computational models of both WM and language processing. |
Cognitive Neuroscience | 15:00 – 15:15 Short talk | Automatic and Selective Inhibition in the Brain: A MEG and Selective Stop Task Study Heather Statham Cardiff University More details Less details
Co-authors: Dr Aline Bompas, Professor Krish Singh, Philip Schmid
Abstract: The stop-signal reaction time (SSRT) is widely used to quantify action inhibition in manual and saccadic tasks. However, it is criticized for its limited reliability (Hedge et al., 2018, Behaviour Research Methods) and its dependency on visual and motor delays (https://mathpsych.org/presentation/1061). Still, many neurophysiological studies rely on SSRT to identify neural markers of inhibition such as increased beta-band oscillations, and P300 and N100 event-related potential (ERP) components. The selective stopping task offers more informative indices by having participants give speeded responses to lateralized dots on go trials, but withhold responses when a stop signal appears, or still respond when an ignore signal appears. The time at which reaction time distributions diverge between go trials and signal-present trials reflects the minimum estimate of visual and motor delays, termed visuomotor deadtime (VMDT). The time at which stop and ignore distributions diverge, denoted Ts, marks the earliest time that top-down, instruction-relevant signals can influence action. Additionally, peak latencies of partial response electromyography (prEMG) can be used to index the timing of inhibition as they reflect when an initiated muscle response has been interrupted before a full response can be recorded (Raud et al., 2022, eLife). We will outline the study and analysis plan of a manual selective stopping task in MEG. Our aim is to isolate the neural mechanisms of automatic (task-unrelated) and selective (task-related) inhibition. For each process, we will identify 1) trials where this process has most likely occurred, and 2) comparable control trials where it hasn’t. To do so, we will use trial types (go, ignore and stop) and their behavioural outcomes (no responses and response times in relation to key behavioural landmarks: VMDT, Ts and prEMG peak latencies). We will compare the oscillatory power across trials to identify when (in a trial) and where (in the brain) differences occur. Specifically, a marker for selective inhibition should distinguish 1) successful stop trials with a prEMG after Ts, and 2) successful ignore trials with a response time longer than Ts. For this marker to provide a credible mechanism for selective inhibition, it would need to be frontocentral and start before Ts. Similarly, a marker of automatic inhibition should distinguish activity in the motor cortices between go and signal-present trials with response times between VMDT and Ts. |
Cognitive Neuroscience | 15:15 – 15:30 Short talk | A Distinct Neural Oscillatory Basis for Perspective-Taking in Autism Klaus Kessler University College Dublin More details Less details
Co-authors: Klaus Kessler, Robert Seymour, Gina Rippon, Hongfang Wang
Abstract: Understanding that others may see the world differently from ourselves is a vital developmental milestone, closely tied to visuospatial perspective taking—specifically, the ability to mentally adopt another person’s visual perspective (level-2 perspective taking). Given that many autistic individuals experience challenges with this type of mental transformation and often face social difficulties later in life, this study explored differences in visual perspective-taking abilities between autistic and non-autistic adolescents. Perspective-taking is a complex cognitive skill central to social understanding. It typically involves an an embodied mental transformation whereby people mentally rotate themselves away from their physical location into the other’s orientation. This mental shift is known to engage theta-band (3–7 Hz) brain oscillations within a fronto-parietal network, including the temporoparietal junction—a pattern established in prior research (e.g., Seymour et al., 2018; Wang et al., 2016; Gooding-Williams et al., 2025). Previous studies suggest that individuals with autism spectrum disorder (ASD) often struggle with such embodied strategies. To examine the neurophysiological mechanisms underlying these differences, we used (cryogenic) magnetoencephalography alongside a validated perspective-taking task in 18 autistic and 17 age-matched non-autistic adolescents. Results showed that as the angular disparity between the participant’s and the avatar’s viewpoint increased, autistic participants exhibited significantly slower reaction times. This behavioural effect was mirrored by a reduction in theta power across a broad network of regions typically active during social cognitive tasks. Interestingly, autistic adolescents also showed greater decreases in alpha power within the visual cortex, regardless of task condition. These findings—reduced theta activity, increased alpha suppression, and steeper increases in response time with angular disparity—suggest that autistic individuals may rely on alternative cognitive strategies, such as mentally rotating objects, rather than simulating another’s perspective through embodied transformation. Notably, when participants were asked to simply track rather than adopt another’s perspective, no group differences emerged in behaviour or neural oscillations. This indicates that the observed differences are specific to high-level, embodied perspective-taking rather than to simpler social attention processes. |
Cognitive Neuroscience | 15:30 – 15:45 Short talk | MEG signatures of BOLD: Characterising between subject-variability in contralateral and ipsilateral motor responses to unilateral finger abductions Daniel Griffiths-King Aston University More details Less details
Co-authors: Daniel Griffiths-King, Sian Worthen, Caroline Witton, Paul Furlong, Michael Hall and Stephen Mayhew
Abstract: Human behaviour relies on collaborative and antagonistic brain activity. In unilateral sensorimotor tasks, fMRI reveals positive and negative BOLD responses (PBR/NBR) in the contralateral and ipsilateral sensory cortices respectively (Nelson & Mayhew, 2024), but their neural basis remains poorly understood. We used MEG to examine broadband oscillatory responses during unilateral motor tasks, to identify contralateral and ipsilateral signatures that might underlie PBR and NBR. Most previous studies focus on the positive motor BOLD component (e.g. Stevenson et al., 2011), overlooking potential ipsilateral contributions. We analysed a subset of the MEGUK dataset (35 adults recruited from Aston University). Participants performed right-hand finger abductions following visual grating offset (1.5–2s duration; 8s inter-trial interval). MEG & EMG data were processed with MNE-Python (v1.8.0) using the MNE-BIDs pipeline. Source activity was reconstructed in the primary motor cortex (M1) via LCMV beamforming, using Freesurfer-derived anatomical models. Analyses targeted three time–frequency windows: (i) beta (15–30 Hz) ERD (event-related desynchronisation; −500–500 ms), (ii) PMBR (post-movement beta rebound; 1000–2000 ms), and (iii) gamma (60–90 Hz) ERS (event-related synchronisation; −500–500 ms), all time-locked to EMG peak onset. Peak source activity was localised within contralateral & ipsilateral precentral gyri, defining M1 regions of interest (ROIs) resulting in 6 virtual electrode (VE) locations per participant. Group-level TFRs (via DPSS multitapers) showed bilateral ERD & PMBR, but with stronger contralateral dominance. PMBR VE time series showed similar peak amplitude & latency across hemispheres. However, individual TFRs revealed variability, including absent contralateral ERD, or even reversed lateralisation of PMBR/ERD. While intra-individual MEG response consistency is well-characterised (e.g. Espenhahn et al., 2017), variability across individuals—especially in ipsilateral responses—remains underexplored. ECoG recordings show fMRI visual cortex NBR is associated with an absence of high frequency band responses (Fracasso et al, 2022) whilst rodent optical imaging spectroscopy studies indicate gamma-band power reductions related to negative hemodynamic responses (Boorman et al, 2015). However, we found no definitive differences in oscillatory activity, including motor-gamma, within ipsilateral hemisphere suggestive of mechanisms which may underpin NBR. |
15:45 – 16:15 | Tea break Ground Floor | |
Oscillations and rhythmic MEG | 16:15 – 16:45 Long talk | Multi-sensory rhythmic stimulation of hippocampal theta to modulate episodic memory in humans Eleonora Marcantoni University of Glasgow More details Less details
Co-authors: Eleonora Marcantoni , Danying Wang, Robin Ince, Dan Bush, Lauri Parkkonen, Satu Palva, Simon Hanslmayr
Abstract: Hippocampal theta oscillations play a critical role in binding multisensory information into coherent episodic memories. Recent evidence suggests that externally entraining these oscillations via 4-Hz audio-visual Rhythmic Sensory Stimulation (RSS) can significantly enhance memory performance in associative memory tasks. However, the current “one-size-fits-all†stimulation approach overlooks individual differences in neural dynamics, potentially contributing to the variability observed in behavioral outcomes. To address this limitation, we developed a pipeline to estimate the individual’s hippocampal theta frequency during a memory task and adapt the stimulation frequency in real time. The pipeline comprises several key steps. First, hippocampal signals are extracted from MEG recordings using an LCMV beamformer. Next, Generalized Eigenvalue Decomposition (GED) is applied to isolate theta-band activity from the broadband signal. Finally, the Cyclic Homogeneous Oscillation (CHO) detection method is used to verify the presence of oscillations and identify their central frequency. This frequency is then used to dynamically adjust the flickering rate of the sensory stimuli during the task. As a proof of concept, we first validated the use of GED and CHO on rodent LFP data by attempting to replicate the well-established correlation between running speed and hippocampal theta frequency. The results confirmed the feasibility of this approach, with the pipeline successfully reproducing the expected relationship (R = 0.27, p < .001). Subsequently, we applied the full pipeline offline to a human MEG dataset collected during an associative memory task involving 4-Hz RSS. Our aim was to evaluate whether the pipeline could detect stimulation-induced changes in hippocampal theta frequency. As hypothesized, the estimated frequencies during stimulation were significantly closer to 4 Hz compared to pre- and post-stimulation windows (main effect of time: F(6,120) = 24.99, p < .001, η² = 0.315). Currently, we are validating the pipeline using a simultaneous MEG-iEEG dataset, allowing us to compare the frequencies estimated from MEG with ground-truth hippocampal activity recorded via iEEG. This step will offer critical insights into the accuracy and reliability of the approach. Preliminary results indicate that real-time detection and tracking of individual theta frequencies is feasible, supporting the potential to test personalised RSS in memory enhancement. |
Oscillations and rhythmic MEG | 16:45 – 17:00 Short talk | Subcortical Contributions to Oscillatory and Behavioural Asymmetries: Insights from the Hemispheric Laterality of Basal Ganglia and Thalamus Tara Ghafari University of Oxford More details Less details
Co-authors: Tara Ghafari, Mohammad Ebrahim Katebi, Mohammad Hossein Ghafari, Aliza Finch, Ole Jensen
Abstract: Healthy individuals exhibit a subtle leftward attentional bias known as pseudoneglect, typically attributed to right-hemisphere dominance for attention. While cortical contributions are well-established, the role of subcortical structures remains less clear. In this study, we explored how naturally occurring volumetric asymmetries in subcortical regions relate to both behavioural and neurophysiological markers in healthy adults. In a behavioural experiment with 44 participants, we assessed spatial bias using a computerised landmark task and eye-tracking, quantifying the point of subjective equality (PSE). Structural T1-weighted MRI data were processed using FSL FIRST to calculate lateralised volumes (LVs) of seven subcortical structures. General linear model analyses revealed that individual differences in PSE were significantly predicted by the lateralised volume of the putamen, suggesting a subcortical origin for individual variation in attentional bias. Complementing this, we analysed resting-state MEG data from a larger cohort (n = 590, Cam-CAN dataset), correlating frequency-specific hemispheric power asymmetries with subcortical volume asymmetries. We found significant associations between the lateralisation of oscillatory power and subcortical volumes. Notably, the putamen showed correlations with lateralised power in the beta band, the thalamus was significantly correlated with alpha laterality and the hippocampus with laterality in the delta/theta bands. Together, these findings provide converging evidence that subcortical volumetric asymmetries not only shape behavioural hemifield biases in spatial attention but also influence the lateralisation of neocortical oscillatory activity. This work highlights the importance of subcortical structures in supporting attentional processes in the healthy brain and lays the groundwork for future research into their role in neurodegenerative disorders. |
Oscillations and rhythmic MEG | 17:00 – 17:15 Short talk | Neuronal correlates of predictive distractor suppression Oscar Ferrante University of Birmingham More details Less details
Co-authors: Ole Jensen, Clayton Hickey
Abstract: Visual attention is influenced by the statistical regularities of our environment, with spatially predictable distractors being actively suppressed. Yet, the neural mechanisms underlying this suppression remain poorly understood. In this talk, I will show how we have used magnetoencephalography (MEG), rapid invisible frequency tagging (RIFT), and multivariate decoding analysis to provide new insight on the processing of predicted distractor locations in the human brain. Using a statistical learning visual search task where a colour-singleton distractor appeared more frequently on one side of the visual field, we found that early visual cortex exhibited reduced neural excitability in the pre-search interval at retinotopic sites corresponding to higher distractor probabilities. During this period, a temporo-occipital network encoded these distractor locations, supporting the hypothesis that proactive suppression directs visual attention away from predictable distractors. Notably, the neural activity associated with pre-search distractor processing extended into the post-search period during late attentional stages (around 200 ms), suggesting a mechanistic link between proactive and reactive distractor suppression. These findings offer critical insights into the neuronal correlates of predictive distractor suppression and provide a deeper understanding of the cognitive mechanisms underlying selective attention. |
Oscillations and rhythmic MEG | 17:15 – 17:30 Short talk | Pre-stimulus shape predictions fluctuate at alpha rhythms and bias subsequent perception Dorottya Hetenyi University College London More details Less details
Co-authors: Dorottya Hetenyi & Peter Kok
Abstract: Predictions about future events significantly influence how we process sensory signals. In previous work, we demonstrated that predicted shape representations exhibit oscillatory activity in the alpha band (10–11 Hz) during pre-stimulus intervals. In that study, participants performed a task that was orthogonal to the shape predictions. Here, we extended these findings by having participants perform a shape identification task that directly relied on the shape predictions, allowing us to link the neural correlates of prediction to subjective perception. We used magnetoencephalography (MEG) combined with multivariate decoding to examine the content and frequency characteristics of perceptual predictions and relate them to behaviour. The shape identification task involved auditory cues predicting which shape was likely to appear. To make the identification of the shapes challenging, they were embedded in white noise. First, we found that valid prediction cues improved both identification accuracy and reaction times. Signal detection theory analyses revealed that participants were significantly biased toward reporting the predicted shape (i.e., reduced criterion), without a change in sensitivity (i.e., similar d-prime). We replicated our previous finding that predicted shape representations fluctuate in the alpha band (10–11 Hz). Logistic regression analyses further revealed that this shape-specific alpha power predicted perceptual biases induced by the predictions. That is, when shape-specific alpha power was high, participants were more likely to perceive the predicted shape. In contrast, higher raw sensor-level occipital alpha power was associated with a greater likelihood of reporting the unpredicted shape. These results suggest that content-specific alpha fluctuations and general occipital alpha power serve distinct functions in visual perception. Taken together, our findings demonstrate that sensory predictions are represented in pre-stimulus alpha oscillations and that these oscillatory signals shape how we perceive the world. |
Oscillations and rhythmic MEG | 17:30 – 17:45 Short talk | Human Hippocampal Theta-Gamma Coupling Coordinates Sequential Planning During Navigation Zimo Huang University College London More details Less details
Co-authors: James Bisby, Neil Burgess, Daniel Bush
Abstract: Human behaviour often relies on executing a specific sequence of actions to achieve a desired outcome. However, the neural mechanisms underlying the dynamic construction and maintenance of such sequences during goal-directed behaviour are not yet clear. Empirical and theoretical studies of working memory function suggest that sequential information may be encoded in neural circuits by bursts of gamma activity occurring at consecutive theta phases. Here, we asked whether similar coding schemes might support sequential planning during goal-directed navigation. Using non-invasive magnetoencephalography and an abstract navigation task, we found that hippocampal theta power during both planning and subsequent navigation decreased with proximity to the current goal, only during accurate navigation. At the same time, theta-gamma phase-amplitude coupling increased with goal proximity, consistent with sequences of upcoming locations being represented by gamma bursts occurring at successive theta phases. Importantly, entorhinal high gamma and hippocampal low gamma dominated while traversing novel and previously experienced paths, respectively, consistent with previous rodent studies. These findings suggest that hippocampal theta-gamma phase amplitude coupling flexibly and dynamically coordinates sequences of actions during goal-directed behaviour across mammalian species, using different gamma bands for mnemonic and prospective planning. |
19:00 – 22:00 | Social evening with drinks and buffet Coin Laundry, EC1R 4QP |
09:00 – 09:20
Coffee and Registration
Ground Floor
Ground Floor
09:20 – 09:50
Coffee Break; Business meeting
Ground Floor; Dickins Library
Ground Floor; Dickins Library
09:50 – 10:00
Opening remarks
Yulia Bezsudnova, Gareth Barnes
University College London
Yulia Bezsudnova, Gareth Barnes
University College London
Dementia Research
10:00 – 10:30
Long talk
Long talk
Clinical Utility of MEG in Dementia Care: Insights from Outpatient Experience
Yoshihito Shigihara
Hokuto Hospital
Yoshihito Shigihara
Hokuto Hospital
More details Less details
Co-authors: Hideyuki Hoshi, Momoko Kobayashi, Keisuke Fukasawa, Keita Shibamiya, Sayuri Ichikawa, Yoko Hirata
Abstract:
Dementia is a functionally defined condition in which various brain diseases lead to cognitive impairments that interfere with daily living. The severity of these impairments does not always correspond directly to the severity of the underlying disease, as multiple factors—such as lifestyle—modulate this relationship. Clinically, we often observe that patients show cognitive improvements after receiving well-being advice from clinicians, even when the causative disease is progressive. This highlights the need for effective tools to monitor treatment outcomes. While neuropsychological assessments are valuable, they have inherent limitations, such as learning and ceiling effects. Magnetoencephalography (MEG) offers complementary insights by capturing brain activity associated with cognitive states, particularly during the rest. Resting-state MEG provides rich information that can be used to infer both functional and pathological brain changes. Since 2019, we have routinely used MEG in our outpatient department for the assessment and treatment of dementia, accumulating experience with over 500 patients reporting subjective and/or objective cognitive impairments. Our findings include: 1. Different spectral parameters of MEG data are associated with distinct aspects of cognitive function. 2. These parameters also correlate with cerebral blood flow (assessed via ultrasonography) and pathological changes (measured using single-photon emission computed tomography). 3. Nonpharmacological treatments improve patients’ cognitive states, and these improvements are reflected in changes in MEG-recorded brain activity. 4. Clinical staff’s subjective impressions of cognitive improvement align more closely with changes in MEG data than with neuropsychological test scores. 5. MEG can predict cognitive improvement following nonpharmacological interventions. In this presentation, we summarise these findings and discuss the future role of MEG in clinical practice, with the goal of enhancing patient well-being. We propose that ‘MEG’ stands for ‘Make Everyone Good’, reflecting its potential to support a more holistic and human-centred approach to dementia care.
Abstract:
Dementia is a functionally defined condition in which various brain diseases lead to cognitive impairments that interfere with daily living. The severity of these impairments does not always correspond directly to the severity of the underlying disease, as multiple factors—such as lifestyle—modulate this relationship. Clinically, we often observe that patients show cognitive improvements after receiving well-being advice from clinicians, even when the causative disease is progressive. This highlights the need for effective tools to monitor treatment outcomes. While neuropsychological assessments are valuable, they have inherent limitations, such as learning and ceiling effects. Magnetoencephalography (MEG) offers complementary insights by capturing brain activity associated with cognitive states, particularly during the rest. Resting-state MEG provides rich information that can be used to infer both functional and pathological brain changes. Since 2019, we have routinely used MEG in our outpatient department for the assessment and treatment of dementia, accumulating experience with over 500 patients reporting subjective and/or objective cognitive impairments. Our findings include: 1. Different spectral parameters of MEG data are associated with distinct aspects of cognitive function. 2. These parameters also correlate with cerebral blood flow (assessed via ultrasonography) and pathological changes (measured using single-photon emission computed tomography). 3. Nonpharmacological treatments improve patients’ cognitive states, and these improvements are reflected in changes in MEG-recorded brain activity. 4. Clinical staff’s subjective impressions of cognitive improvement align more closely with changes in MEG data than with neuropsychological test scores. 5. MEG can predict cognitive improvement following nonpharmacological interventions. In this presentation, we summarise these findings and discuss the future role of MEG in clinical practice, with the goal of enhancing patient well-being. We propose that ‘MEG’ stands for ‘Make Everyone Good’, reflecting its potential to support a more holistic and human-centred approach to dementia care.
Dementia Research
10:30 – 10:45
Short talk
Short talk
MEG network dynamics offer enhanced sensitivity for detecting amyloid pathology and disease progression in Alzheimer’s disease
Mats van Es
University of Oxford
Mats van Es
University of Oxford
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Co-authors: Mats W.J. van Es, Andrew J. Quinn, Jemma Pitt, Tony Thayanandan, Marlou N Perquin, Alexandra Krugliak, Ece Kocagoncu, Juliette Lanskey, Chetan Gohil, Vanessa Raymont, James B. Rowe, Anna C. Nobre, Mark W. Woolrich
Abstract:
Current diagnosis and monitoring of Alzheimer’s Disease (AD) focus on Amyloid-beta, Tau aggregates, and atrophy. To advance treatments, new biomarkers are needed that are sensitive, reliable, and predictive of disease progression. We evaluated MEG spectral density in early symptomatic AD. We used data from the New Therapeutics in Alzheimer’s Disease (NTAD) study [Lanskey et al., 2022]: participants aged 50-85 with mild cognitive impairment or early AD (n=67, biomarker positive) and normal cognition (n=34, biomarker negative). Independent Cam-CAN data (N=612) were used to model confounds, including age, sex, and scanner effects. We examined spectral activity during resting wakefulness. First, we assessed static spectral power to replicate previous findings. Next, we applied Hidden-Markov Modelling (HMM) [Vidaurre et al., 2018] with 10 states to investigate brain network dynamics as a potentially more sensitive biomarker. We assessed cross-sectional differences (amyloid groups) and longitudinal changes (baseline to annual follow-up in amyloid-positive participants), and evaluated two-week test-retest reliability using intraclass correlation coefficient (ICC). We replicated previous findings of oscillatory slowing in AD: increased delta/theta and decreased alpha/beta power. These effects were robust at the group level but small to moderate in size (Cohen’s f2 < 0.35). Similar trends appeared in brain network spectra, with sensitivity varying by network and frequency band. Effect sizes exceeded those of static spectra in 6/10 states, and were strongest in a parietal alpha network (Cohen’s f2 > 0.7) in the alpha/beta band. Excluding one network, power in all networks was reliable (ICC > 0.8) and more reliable than static features. Longitudinally, the most pronounced changes occurred in a distinct network and frequency band compared to cross-sectional differences: patients showed reduced high gamma power (44-120 Hz) in a frontal network (Cohen’s f2 > 1.0), an effect only hinted at in static spectra. These results indicate that brain network dynamics are sensitive to amyloid status and disease progression, and that network spectra are more sensitive and reliable than static spectra. This suggests promise as a biomarker tool. Future analyses will examine correlations with cognitive scores and other biomarkers.
Abstract:
Current diagnosis and monitoring of Alzheimer’s Disease (AD) focus on Amyloid-beta, Tau aggregates, and atrophy. To advance treatments, new biomarkers are needed that are sensitive, reliable, and predictive of disease progression. We evaluated MEG spectral density in early symptomatic AD. We used data from the New Therapeutics in Alzheimer’s Disease (NTAD) study [Lanskey et al., 2022]: participants aged 50-85 with mild cognitive impairment or early AD (n=67, biomarker positive) and normal cognition (n=34, biomarker negative). Independent Cam-CAN data (N=612) were used to model confounds, including age, sex, and scanner effects. We examined spectral activity during resting wakefulness. First, we assessed static spectral power to replicate previous findings. Next, we applied Hidden-Markov Modelling (HMM) [Vidaurre et al., 2018] with 10 states to investigate brain network dynamics as a potentially more sensitive biomarker. We assessed cross-sectional differences (amyloid groups) and longitudinal changes (baseline to annual follow-up in amyloid-positive participants), and evaluated two-week test-retest reliability using intraclass correlation coefficient (ICC). We replicated previous findings of oscillatory slowing in AD: increased delta/theta and decreased alpha/beta power. These effects were robust at the group level but small to moderate in size (Cohen’s f2 < 0.35). Similar trends appeared in brain network spectra, with sensitivity varying by network and frequency band. Effect sizes exceeded those of static spectra in 6/10 states, and were strongest in a parietal alpha network (Cohen’s f2 > 0.7) in the alpha/beta band. Excluding one network, power in all networks was reliable (ICC > 0.8) and more reliable than static features. Longitudinally, the most pronounced changes occurred in a distinct network and frequency band compared to cross-sectional differences: patients showed reduced high gamma power (44-120 Hz) in a frontal network (Cohen’s f2 > 1.0), an effect only hinted at in static spectra. These results indicate that brain network dynamics are sensitive to amyloid status and disease progression, and that network spectra are more sensitive and reliable than static spectra. This suggests promise as a biomarker tool. Future analyses will examine correlations with cognitive scores and other biomarkers.
Dementia Research
10:45 – 11:00
Short talk
Short talk
Practice-induced reductions in Gamma power in Response to Proper Name Anomia Therapy in people with dementia: An MEG Study
Aygun Badalova
University College London
Aygun Badalova
University College London
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Co-authors: Aygun Badalova 1,3 Tae Twomey 1,3, Vladimir Litvak 4 George O’Neill 4 Alex Leff 1,2,3
Abstract:
Objective Proper name anomia is a common language deficit observed in people with dementia (PWD), impacting their ability to recall and retrieve the names of familiar people. This study investigates the neural changes associated with a 6-week, app-based, proper-name anomia therapy in PWD using MEG and whether this learning-based therapy leads to changes in gamma-band oscillatory activity within the left superior temporal gyrus (STG).The left STG was chosen for its key role in language processing and name retrieval. Methods 26 PWD with proper name anomia were recruited. Following baseline assessment, patients underwent a structured 6-week proper-name anomia therapy program using a novel app called Gotcha! Participants were trained to name 6-10 faces (usually their relatives and close friends), using confrontation naming and audio cueing methods. MEG recordings were obtained at two time points: pre- and post-therapy while PWD were presented with pictures of the trained familiar or untrained, but famous faces, which they named aloud. MEG data were analysed in SPM, we measured source localised gamma-band (30-80 Hz) power 0-3400 ms after the onset of a face We ran a 2×2 factorial analysis on our source images (famous v familiar; pre- v post-therapy) using a repeated-measures ANOVA to look for changes in power across conditions. The behavioural data was analysed using a repeated-measures ANOVA with the outcome being correctly named faces while free-naming. Results Behavioural data analysis revealed that the Gotcha! therapy app is effective with a significant effect at the group level of training > baseline, F(1,36)=55.47, p=0.01. For the MEG analysis, we identified a large cluster of 1205 voxels situated in the left superior temporal gyrus (MNI: -54 10 -6, F=11.92, p=0.016 peak level FWE-corrected over the left STG) where gamma reduction was associated with training (pre-post) of familiar faces, but not (untrained) famous faces. This is the first study to demonstrate that this region also supports re-learning for familiar face-name associations in PWD. Discussion App-based proper name anomia retraining appears to be an effective therapy for PWD. Initial MEG findings suggest that therapy effects are manifest in areas associated with face-naming.
Abstract:
Objective Proper name anomia is a common language deficit observed in people with dementia (PWD), impacting their ability to recall and retrieve the names of familiar people. This study investigates the neural changes associated with a 6-week, app-based, proper-name anomia therapy in PWD using MEG and whether this learning-based therapy leads to changes in gamma-band oscillatory activity within the left superior temporal gyrus (STG).The left STG was chosen for its key role in language processing and name retrieval. Methods 26 PWD with proper name anomia were recruited. Following baseline assessment, patients underwent a structured 6-week proper-name anomia therapy program using a novel app called Gotcha! Participants were trained to name 6-10 faces (usually their relatives and close friends), using confrontation naming and audio cueing methods. MEG recordings were obtained at two time points: pre- and post-therapy while PWD were presented with pictures of the trained familiar or untrained, but famous faces, which they named aloud. MEG data were analysed in SPM, we measured source localised gamma-band (30-80 Hz) power 0-3400 ms after the onset of a face We ran a 2×2 factorial analysis on our source images (famous v familiar; pre- v post-therapy) using a repeated-measures ANOVA to look for changes in power across conditions. The behavioural data was analysed using a repeated-measures ANOVA with the outcome being correctly named faces while free-naming. Results Behavioural data analysis revealed that the Gotcha! therapy app is effective with a significant effect at the group level of training > baseline, F(1,36)=55.47, p=0.01. For the MEG analysis, we identified a large cluster of 1205 voxels situated in the left superior temporal gyrus (MNI: -54 10 -6, F=11.92, p=0.016 peak level FWE-corrected over the left STG) where gamma reduction was associated with training (pre-post) of familiar faces, but not (untrained) famous faces. This is the first study to demonstrate that this region also supports re-learning for familiar face-name associations in PWD. Discussion App-based proper name anomia retraining appears to be an effective therapy for PWD. Initial MEG findings suggest that therapy effects are manifest in areas associated with face-naming.
Dementia Research
11:00 – 11:15
Short talk
Short talk
Electrophysiological correlates of the Last-In-First-Out hypothesis of age-related white matter decline.
Atheer Al-Manea
University of Birmingham
Atheer Al-Manea
University of Birmingham
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Co-authors: Magda Chechlacz & Andrew J Quinn
Abstract:
The Last-In-First-Out (LIFO) hypothesis proposes that phylogenetically newer, later-myelinating brain regions are more vulnerable to age-related degeneration than evolutionarily older structures. However, the electrophysiological correlates of this structural aging pattern remain poorly understood. We will test whether peak alpha frequency and power decline are more impacted by variability in anterior or posterior tracts of the corpus callosum. The alpha rhythm is spatially localized closer to the posterior tracts whereas the LIFO hypothesis suggests that the anterior tracts are more susceptible to age related deterioration. We combined high-resolution diffusion MRI tractography, SIFT2 streamline weighting, and volumetric analyses in 542 adults (18–88 y) from the Cam-CAN ageing cohort, using the multimodal micapipe (v0.2.3) pipeline, to chart age-related white matter decline across three corpus callosum (CC) segments: Forceps Minor (FMI), mid-body (CC_MID), and Forceps Major (FMA). Segmentation of these anterior, middle, and posterior callosal bundles revealed a pronounced anterior-to-posterior gradient of deterioration. The Forceps Minor exhibited the most substantial decline in both volume and weighted fractional anisotropy (FA), while mid-body demonstrated intermediate vulnerability, and Forceps Major showed relative preservation. Standard diffusion tensor-imaging (DTI) metrics (mean FA) failed to detect subtle mid-body and posterior declines whereas SIFT2-weighted FA revealed robust negative age slopes. Volumes declined steeply in all segments, and quadratic models further revealed accelerated deterioration in later decades. This replicated the pattern of structural connectivity suggested by the LIFO hypothesis. A GLM-Spectrum analysis predicting individual variability in the resting state power spectrum shows the strongest effects with the anterior corpus callosum compared to the middle, or posterior tracts. This structure-function dissociation refines the LIFO model by integrating advanced tractography and electrophysiological metrics to capture divergent aging trajectories in the human brain’s structure and function.
Abstract:
The Last-In-First-Out (LIFO) hypothesis proposes that phylogenetically newer, later-myelinating brain regions are more vulnerable to age-related degeneration than evolutionarily older structures. However, the electrophysiological correlates of this structural aging pattern remain poorly understood. We will test whether peak alpha frequency and power decline are more impacted by variability in anterior or posterior tracts of the corpus callosum. The alpha rhythm is spatially localized closer to the posterior tracts whereas the LIFO hypothesis suggests that the anterior tracts are more susceptible to age related deterioration. We combined high-resolution diffusion MRI tractography, SIFT2 streamline weighting, and volumetric analyses in 542 adults (18–88 y) from the Cam-CAN ageing cohort, using the multimodal micapipe (v0.2.3) pipeline, to chart age-related white matter decline across three corpus callosum (CC) segments: Forceps Minor (FMI), mid-body (CC_MID), and Forceps Major (FMA). Segmentation of these anterior, middle, and posterior callosal bundles revealed a pronounced anterior-to-posterior gradient of deterioration. The Forceps Minor exhibited the most substantial decline in both volume and weighted fractional anisotropy (FA), while mid-body demonstrated intermediate vulnerability, and Forceps Major showed relative preservation. Standard diffusion tensor-imaging (DTI) metrics (mean FA) failed to detect subtle mid-body and posterior declines whereas SIFT2-weighted FA revealed robust negative age slopes. Volumes declined steeply in all segments, and quadratic models further revealed accelerated deterioration in later decades. This replicated the pattern of structural connectivity suggested by the LIFO hypothesis. A GLM-Spectrum analysis predicting individual variability in the resting state power spectrum shows the strongest effects with the anterior corpus callosum compared to the middle, or posterior tracts. This structure-function dissociation refines the LIFO model by integrating advanced tractography and electrophysiological metrics to capture divergent aging trajectories in the human brain’s structure and function.
11:15 – 11:45
Tea break
Ground Floor
Ground Floor
Dynamics
11:45 – 12:00
Short talk
Short talk
Distinct spectral profiles of ageing and neurodegeneration
Andrew Quinn
University of Birmingham
Andrew Quinn
University of Birmingham
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Co-authors: Andrew J. Quinn, Mats W.J. van Es, Jemma Pitt, Tony Thayanandan, Marlou N Perquin, Alexandra Krugliak, Ece Kocagoncu, Juliette Lanskey, Chetan Gohil, Vanessa Raymont, James B. Rowe, Anna C. Nobre, Mark W. Woolrich
Abstract:
Non-invasive recordings of brain electrophysiology offer insight into age-related decline and disease related degeneration of neuronal function. These changes are reflected by alterations in the power spectrum of EEG and MEG recordings. Statistically rigorous analysis methodologies are needed to translate these findings into clinically meaningful metrics that address the global challenge of maintaining brain health in ageing populations. We us the CamCAN dataset to identify a full-frequency profile of the ageing effect on resting state electrophysiology and establish a basis for effect size calculation on the spectrum. Specific oscillations within this profile have different effect sizes indicating that sample size planning for ageing effects must consider the specific features of interest. The frequency profile of ageing is strongly robust to a range of common covariates and partially robust to modelling of grey matter volume. We establish that a well powered sample may become underpowered when analyses look to establish the age effect that is linearly separable from an age-relevant covariate such as grey matter volume. These results help to consolidate a variable literature of age effects on resting state brain electrophysiology and provide a pathway towards formal comparison and assessment of candidate markers for brain health in ageing. These results are used as the basis to explore the distinction between Alzheimer’s Disease (AD) and healthy ageing, and specifically whether neurodegeneration can be considered a form of accelerated brain ageing. We used data from the New Therapeutics in Alzheimer’s Disease (NTAD) study to compute full-frequency profiles of ageing and of presence of Alzheimer’s pathology. The results show distinct spectral profiles for each predictor indicating that although age is a strong risk factor for neurodegeneration it has a separate impact on neuronal function. Crucially, the full spectral profiles showed a distinction between ageing and neurodegeneration, they can have highly correlated spatial effects at individual frequencies. Specifically, both ageing and the presence of AD lead to a decrease in posterior spectral power in the high alpha range, whereas they have distinct effects in the beta range. This result suggests that both high sensitivity for AD pathology and separability close covariates must both be optimised when searching for clinical markers.
Abstract:
Non-invasive recordings of brain electrophysiology offer insight into age-related decline and disease related degeneration of neuronal function. These changes are reflected by alterations in the power spectrum of EEG and MEG recordings. Statistically rigorous analysis methodologies are needed to translate these findings into clinically meaningful metrics that address the global challenge of maintaining brain health in ageing populations. We us the CamCAN dataset to identify a full-frequency profile of the ageing effect on resting state electrophysiology and establish a basis for effect size calculation on the spectrum. Specific oscillations within this profile have different effect sizes indicating that sample size planning for ageing effects must consider the specific features of interest. The frequency profile of ageing is strongly robust to a range of common covariates and partially robust to modelling of grey matter volume. We establish that a well powered sample may become underpowered when analyses look to establish the age effect that is linearly separable from an age-relevant covariate such as grey matter volume. These results help to consolidate a variable literature of age effects on resting state brain electrophysiology and provide a pathway towards formal comparison and assessment of candidate markers for brain health in ageing. These results are used as the basis to explore the distinction between Alzheimer’s Disease (AD) and healthy ageing, and specifically whether neurodegeneration can be considered a form of accelerated brain ageing. We used data from the New Therapeutics in Alzheimer’s Disease (NTAD) study to compute full-frequency profiles of ageing and of presence of Alzheimer’s pathology. The results show distinct spectral profiles for each predictor indicating that although age is a strong risk factor for neurodegeneration it has a separate impact on neuronal function. Crucially, the full spectral profiles showed a distinction between ageing and neurodegeneration, they can have highly correlated spatial effects at individual frequencies. Specifically, both ageing and the presence of AD lead to a decrease in posterior spectral power in the high alpha range, whereas they have distinct effects in the beta range. This result suggests that both high sensitivity for AD pathology and separability close covariates must both be optimised when searching for clinical markers.
Dynamics
12:00 – 12:15
Short talk
Short talk
Universal rhythmic architecture uncovers distinct modes of neural dynamics
Ayelet Landau
University College London
Ayelet Landau
University College London
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Co-authors: Golan Karvat, Maité Crespo-García, Gal Vishne, Michael C Anderson
Abstract:
A prominent idea in neuroscience, for over a century, has been that brain activity comprises electrical field potentials that oscillate in different frequency bands. This notion, however, has been critiqued on various grounds. Most recently, evidence suggests that brain oscillations may sometimes appear as transient bursts rather than continuous rhythms. Here, we explore the hypothesis that rhythmicity—whether sustained or bursty—represents an additional organizing principle or dimension of brain function. We analysed neurophysiological spectra of 859 participants covering diverse species, recording methods, ages (18-88), brain regions, and cognitive states in both healthy and disease, using a new rhythmicity measure. Through computer simulations and brain stimulation, we identified a universal spectral architecture comprising two categories: high-rhythmicity bands linked to continuous oscillations and new low-rhythmicity bands characterized by brief bursts. Beyond characterizing this architecture I will discuss its functional consequences and examine whether the two categories of activity relate to two different modes of information processing. Namely, sustained bands reflecting maintenance of ongoing activity, and transient bands indicating responses to changes.
Abstract:
A prominent idea in neuroscience, for over a century, has been that brain activity comprises electrical field potentials that oscillate in different frequency bands. This notion, however, has been critiqued on various grounds. Most recently, evidence suggests that brain oscillations may sometimes appear as transient bursts rather than continuous rhythms. Here, we explore the hypothesis that rhythmicity—whether sustained or bursty—represents an additional organizing principle or dimension of brain function. We analysed neurophysiological spectra of 859 participants covering diverse species, recording methods, ages (18-88), brain regions, and cognitive states in both healthy and disease, using a new rhythmicity measure. Through computer simulations and brain stimulation, we identified a universal spectral architecture comprising two categories: high-rhythmicity bands linked to continuous oscillations and new low-rhythmicity bands characterized by brief bursts. Beyond characterizing this architecture I will discuss its functional consequences and examine whether the two categories of activity relate to two different modes of information processing. Namely, sustained bands reflecting maintenance of ongoing activity, and transient bands indicating responses to changes.
Dynamics
12:15 – 12:30
Short talk
Short talk
The temporal dynamics of speech motor control during imagined speech
Francesco Mantegna
University of Oxford
Francesco Mantegna
University of Oxford
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Co-authors: Joan Orpella, David Poeppel
Abstract:
Speech production constitutes a fundamental activity inherent in our interactions and communication with others. The apparent ease we experience during speech production conceals the inherent complexity of its underlying machinery. The subjective feeling that speech production is seamless derives from extensive prior experience, which we constantly deploy to make predictions and apply corrections as we speak. One convenient way to study these feedforward and feedback control mechanisms is through imagined speech—that is, the internal generation of speech in the absence of motor articulation and its sensory consequences. When speech is conjured up internally, control mechanisms are not overshadowed by brain activity associated with motor execution and sensory feedback, making them more easily identifiable in the brain signal. During my PhD, I conducted three magnetoencephalography (MEG) studies investigating the temporal dynamics of speech motor control during imagined speech. The first study (1) explores how the decodability of sensory and motor transient neural representations associated with imagined speech varies depending on speech content (e.g., consonants vs. vowels). The second study (2) reveals a dynamic shift in the hemispheric lateralization of functional connectivity between motor and auditory areas, suggesting that feedforward control exhibits left lateralization prior to imagined speech production, while feedback control exhibits right lateralization afterward. The third study (3) demonstrates a spatiotemporal segregation of frequency-specific power modulations in the alpha and beta frequency bands in motor and auditory areas, respectively. Additional analyses confirmed that these two frequencies are not harmonics but rather spectrally distinct: a somatomotor ‘mu’ rhythm and an auditory ‘tau’ rhythm. This segregation indicates distinct coding schemes that necessitate sensorimotor coordination during imagined speech. Collectively, these studies contribute to advancing our understanding of speech motor control, offering a more precise temporal characterization of both covert and overt speech production subprocesses and thereby shedding new light on its neural architecture. Moreover, they lay the foundation for a non-invasive brain-computer interface, a topic that I am currently investigating in my postdoc.
Abstract:
Speech production constitutes a fundamental activity inherent in our interactions and communication with others. The apparent ease we experience during speech production conceals the inherent complexity of its underlying machinery. The subjective feeling that speech production is seamless derives from extensive prior experience, which we constantly deploy to make predictions and apply corrections as we speak. One convenient way to study these feedforward and feedback control mechanisms is through imagined speech—that is, the internal generation of speech in the absence of motor articulation and its sensory consequences. When speech is conjured up internally, control mechanisms are not overshadowed by brain activity associated with motor execution and sensory feedback, making them more easily identifiable in the brain signal. During my PhD, I conducted three magnetoencephalography (MEG) studies investigating the temporal dynamics of speech motor control during imagined speech. The first study (1) explores how the decodability of sensory and motor transient neural representations associated with imagined speech varies depending on speech content (e.g., consonants vs. vowels). The second study (2) reveals a dynamic shift in the hemispheric lateralization of functional connectivity between motor and auditory areas, suggesting that feedforward control exhibits left lateralization prior to imagined speech production, while feedback control exhibits right lateralization afterward. The third study (3) demonstrates a spatiotemporal segregation of frequency-specific power modulations in the alpha and beta frequency bands in motor and auditory areas, respectively. Additional analyses confirmed that these two frequencies are not harmonics but rather spectrally distinct: a somatomotor ‘mu’ rhythm and an auditory ‘tau’ rhythm. This segregation indicates distinct coding schemes that necessitate sensorimotor coordination during imagined speech. Collectively, these studies contribute to advancing our understanding of speech motor control, offering a more precise temporal characterization of both covert and overt speech production subprocesses and thereby shedding new light on its neural architecture. Moreover, they lay the foundation for a non-invasive brain-computer interface, a topic that I am currently investigating in my postdoc.
12:30 – 13:00
Flash talks
Flash talks
Session 1 flash talks
Mary Ward Hall
Mary Ward Hall
13:00 – 14:30
Lunch and poster session 1
Ground Floor
Ground Floor
Cognitive Neuroscience
14:30 – 15:00
Long talk
Long talk
Working Memory Reactivation Across Embedded Language Structures
Jiaqi Li
University of Oxford
Jiaqi Li
University of Oxford
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Co-authors: Jiaqi Li, Yali Pan, Hyojin Park, Peter Hagoort, Huan Luo, Ole Jensen
Abstract:
Recursiveness, involving hierarchical embedding of clauses, is a key feature of human language that depends on working memory (WM). During speech comprehension, listeners must maintain previously processed words or phrases for later unification. However, the neural mechanisms underlying how WM supports the processing of complex recursive structures remain unclear. We constructed English sentences with embedded language structures (e.g. The dog, who chases the cat, jumps over the mud.) and recorded magnetoencephalography (MEG) signals while English native speakers listened to these sentences. Neural decoding results demonstrate that during speech comprehension, previously encoded information (e.g. the dog) is maintained in an activity-silent state until syntactic cues (e.g. jumps over) trigger unification. In our study, the verb (e.g. jumps over) reactivated the subject constituent that preceded the embedded clause (e.g. the dog) after 600 ms of the verb’s onset. Furthermore, source-level searchlight analysis reveals that the memory reactivation first occurs in the prefrontal cortex followed by reactivation in the temporal cortex. Further analysis revealed that the syntactic structure of the embedded clause specifically modulated the memory performance related to unification and the strength of memory reactivation. This study provides crucial insights into the temporal and spatial dynamics of WM functions required for unification operations across embedded structures. By bridging the gap between the domains of WM and language comprehension, this work offers a novel perspective with potential implications for refining computational models of both WM and language processing.
Abstract:
Recursiveness, involving hierarchical embedding of clauses, is a key feature of human language that depends on working memory (WM). During speech comprehension, listeners must maintain previously processed words or phrases for later unification. However, the neural mechanisms underlying how WM supports the processing of complex recursive structures remain unclear. We constructed English sentences with embedded language structures (e.g. The dog, who chases the cat, jumps over the mud.) and recorded magnetoencephalography (MEG) signals while English native speakers listened to these sentences. Neural decoding results demonstrate that during speech comprehension, previously encoded information (e.g. the dog) is maintained in an activity-silent state until syntactic cues (e.g. jumps over) trigger unification. In our study, the verb (e.g. jumps over) reactivated the subject constituent that preceded the embedded clause (e.g. the dog) after 600 ms of the verb’s onset. Furthermore, source-level searchlight analysis reveals that the memory reactivation first occurs in the prefrontal cortex followed by reactivation in the temporal cortex. Further analysis revealed that the syntactic structure of the embedded clause specifically modulated the memory performance related to unification and the strength of memory reactivation. This study provides crucial insights into the temporal and spatial dynamics of WM functions required for unification operations across embedded structures. By bridging the gap between the domains of WM and language comprehension, this work offers a novel perspective with potential implications for refining computational models of both WM and language processing.
Cognitive Neuroscience
15:00 – 15:15
Short talk
Short talk
Automatic and Selective Inhibition in the Brain: A MEG and Selective Stop Task Study
Heather Statham
Cardiff University
Heather Statham
Cardiff University
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Co-authors: Dr Aline Bompas, Professor Krish Singh, Philip Schmid
Abstract:
The stop-signal reaction time (SSRT) is widely used to quantify action inhibition in manual and saccadic tasks. However, it is criticized for its limited reliability (Hedge et al., 2018, Behaviour Research Methods) and its dependency on visual and motor delays (https://mathpsych.org/presentation/1061). Still, many neurophysiological studies rely on SSRT to identify neural markers of inhibition such as increased beta-band oscillations, and P300 and N100 event-related potential (ERP) components. The selective stopping task offers more informative indices by having participants give speeded responses to lateralized dots on go trials, but withhold responses when a stop signal appears, or still respond when an ignore signal appears. The time at which reaction time distributions diverge between go trials and signal-present trials reflects the minimum estimate of visual and motor delays, termed visuomotor deadtime (VMDT). The time at which stop and ignore distributions diverge, denoted Ts, marks the earliest time that top-down, instruction-relevant signals can influence action. Additionally, peak latencies of partial response electromyography (prEMG) can be used to index the timing of inhibition as they reflect when an initiated muscle response has been interrupted before a full response can be recorded (Raud et al., 2022, eLife). We will outline the study and analysis plan of a manual selective stopping task in MEG. Our aim is to isolate the neural mechanisms of automatic (task-unrelated) and selective (task-related) inhibition. For each process, we will identify 1) trials where this process has most likely occurred, and 2) comparable control trials where it hasn’t. To do so, we will use trial types (go, ignore and stop) and their behavioural outcomes (no responses and response times in relation to key behavioural landmarks: VMDT, Ts and prEMG peak latencies). We will compare the oscillatory power across trials to identify when (in a trial) and where (in the brain) differences occur. Specifically, a marker for selective inhibition should distinguish 1) successful stop trials with a prEMG after Ts, and 2) successful ignore trials with a response time longer than Ts. For this marker to provide a credible mechanism for selective inhibition, it would need to be frontocentral and start before Ts. Similarly, a marker of automatic inhibition should distinguish activity in the motor cortices between go and signal-present trials with response times between VMDT and Ts.
Abstract:
The stop-signal reaction time (SSRT) is widely used to quantify action inhibition in manual and saccadic tasks. However, it is criticized for its limited reliability (Hedge et al., 2018, Behaviour Research Methods) and its dependency on visual and motor delays (https://mathpsych.org/presentation/1061). Still, many neurophysiological studies rely on SSRT to identify neural markers of inhibition such as increased beta-band oscillations, and P300 and N100 event-related potential (ERP) components. The selective stopping task offers more informative indices by having participants give speeded responses to lateralized dots on go trials, but withhold responses when a stop signal appears, or still respond when an ignore signal appears. The time at which reaction time distributions diverge between go trials and signal-present trials reflects the minimum estimate of visual and motor delays, termed visuomotor deadtime (VMDT). The time at which stop and ignore distributions diverge, denoted Ts, marks the earliest time that top-down, instruction-relevant signals can influence action. Additionally, peak latencies of partial response electromyography (prEMG) can be used to index the timing of inhibition as they reflect when an initiated muscle response has been interrupted before a full response can be recorded (Raud et al., 2022, eLife). We will outline the study and analysis plan of a manual selective stopping task in MEG. Our aim is to isolate the neural mechanisms of automatic (task-unrelated) and selective (task-related) inhibition. For each process, we will identify 1) trials where this process has most likely occurred, and 2) comparable control trials where it hasn’t. To do so, we will use trial types (go, ignore and stop) and their behavioural outcomes (no responses and response times in relation to key behavioural landmarks: VMDT, Ts and prEMG peak latencies). We will compare the oscillatory power across trials to identify when (in a trial) and where (in the brain) differences occur. Specifically, a marker for selective inhibition should distinguish 1) successful stop trials with a prEMG after Ts, and 2) successful ignore trials with a response time longer than Ts. For this marker to provide a credible mechanism for selective inhibition, it would need to be frontocentral and start before Ts. Similarly, a marker of automatic inhibition should distinguish activity in the motor cortices between go and signal-present trials with response times between VMDT and Ts.
Cognitive Neuroscience
15:15 – 15:30
Short talk
Short talk
A Distinct Neural Oscillatory Basis for Perspective-Taking in Autism
Klaus Kessler
University College Dublin
Klaus Kessler
University College Dublin
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Co-authors: Klaus Kessler, Robert Seymour, Gina Rippon, Hongfang Wang
Abstract:
Understanding that others may see the world differently from ourselves is a vital developmental milestone, closely tied to visuospatial perspective taking—specifically, the ability to mentally adopt another person’s visual perspective (level-2 perspective taking). Given that many autistic individuals experience challenges with this type of mental transformation and often face social difficulties later in life, this study explored differences in visual perspective-taking abilities between autistic and non-autistic adolescents. Perspective-taking is a complex cognitive skill central to social understanding. It typically involves an an embodied mental transformation whereby people mentally rotate themselves away from their physical location into the other’s orientation. This mental shift is known to engage theta-band (3–7 Hz) brain oscillations within a fronto-parietal network, including the temporoparietal junction—a pattern established in prior research (e.g., Seymour et al., 2018; Wang et al., 2016; Gooding-Williams et al., 2025). Previous studies suggest that individuals with autism spectrum disorder (ASD) often struggle with such embodied strategies. To examine the neurophysiological mechanisms underlying these differences, we used (cryogenic) magnetoencephalography alongside a validated perspective-taking task in 18 autistic and 17 age-matched non-autistic adolescents. Results showed that as the angular disparity between the participant’s and the avatar’s viewpoint increased, autistic participants exhibited significantly slower reaction times. This behavioural effect was mirrored by a reduction in theta power across a broad network of regions typically active during social cognitive tasks. Interestingly, autistic adolescents also showed greater decreases in alpha power within the visual cortex, regardless of task condition. These findings—reduced theta activity, increased alpha suppression, and steeper increases in response time with angular disparity—suggest that autistic individuals may rely on alternative cognitive strategies, such as mentally rotating objects, rather than simulating another’s perspective through embodied transformation. Notably, when participants were asked to simply track rather than adopt another’s perspective, no group differences emerged in behaviour or neural oscillations. This indicates that the observed differences are specific to high-level, embodied perspective-taking rather than to simpler social attention processes.
Abstract:
Understanding that others may see the world differently from ourselves is a vital developmental milestone, closely tied to visuospatial perspective taking—specifically, the ability to mentally adopt another person’s visual perspective (level-2 perspective taking). Given that many autistic individuals experience challenges with this type of mental transformation and often face social difficulties later in life, this study explored differences in visual perspective-taking abilities between autistic and non-autistic adolescents. Perspective-taking is a complex cognitive skill central to social understanding. It typically involves an an embodied mental transformation whereby people mentally rotate themselves away from their physical location into the other’s orientation. This mental shift is known to engage theta-band (3–7 Hz) brain oscillations within a fronto-parietal network, including the temporoparietal junction—a pattern established in prior research (e.g., Seymour et al., 2018; Wang et al., 2016; Gooding-Williams et al., 2025). Previous studies suggest that individuals with autism spectrum disorder (ASD) often struggle with such embodied strategies. To examine the neurophysiological mechanisms underlying these differences, we used (cryogenic) magnetoencephalography alongside a validated perspective-taking task in 18 autistic and 17 age-matched non-autistic adolescents. Results showed that as the angular disparity between the participant’s and the avatar’s viewpoint increased, autistic participants exhibited significantly slower reaction times. This behavioural effect was mirrored by a reduction in theta power across a broad network of regions typically active during social cognitive tasks. Interestingly, autistic adolescents also showed greater decreases in alpha power within the visual cortex, regardless of task condition. These findings—reduced theta activity, increased alpha suppression, and steeper increases in response time with angular disparity—suggest that autistic individuals may rely on alternative cognitive strategies, such as mentally rotating objects, rather than simulating another’s perspective through embodied transformation. Notably, when participants were asked to simply track rather than adopt another’s perspective, no group differences emerged in behaviour or neural oscillations. This indicates that the observed differences are specific to high-level, embodied perspective-taking rather than to simpler social attention processes.
Cognitive Neuroscience
15:30 – 15:45
Short talk
Short talk
MEG signatures of BOLD: Characterising between subject-variability in contralateral and ipsilateral motor responses to unilateral finger abductions
Daniel Griffiths-King
Aston University
Daniel Griffiths-King
Aston University
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Co-authors: Daniel Griffiths-King, Sian Worthen, Caroline Witton, Paul Furlong, Michael Hall and Stephen Mayhew
Abstract:
Human behaviour relies on collaborative and antagonistic brain activity. In unilateral sensorimotor tasks, fMRI reveals positive and negative BOLD responses (PBR/NBR) in the contralateral and ipsilateral sensory cortices respectively (Nelson & Mayhew, 2024), but their neural basis remains poorly understood. We used MEG to examine broadband oscillatory responses during unilateral motor tasks, to identify contralateral and ipsilateral signatures that might underlie PBR and NBR. Most previous studies focus on the positive motor BOLD component (e.g. Stevenson et al., 2011), overlooking potential ipsilateral contributions. We analysed a subset of the MEGUK dataset (35 adults recruited from Aston University). Participants performed right-hand finger abductions following visual grating offset (1.5–2s duration; 8s inter-trial interval). MEG & EMG data were processed with MNE-Python (v1.8.0) using the MNE-BIDs pipeline. Source activity was reconstructed in the primary motor cortex (M1) via LCMV beamforming, using Freesurfer-derived anatomical models. Analyses targeted three time–frequency windows: (i) beta (15–30 Hz) ERD (event-related desynchronisation; −500–500 ms), (ii) PMBR (post-movement beta rebound; 1000–2000 ms), and (iii) gamma (60–90 Hz) ERS (event-related synchronisation; −500–500 ms), all time-locked to EMG peak onset. Peak source activity was localised within contralateral & ipsilateral precentral gyri, defining M1 regions of interest (ROIs) resulting in 6 virtual electrode (VE) locations per participant. Group-level TFRs (via DPSS multitapers) showed bilateral ERD & PMBR, but with stronger contralateral dominance. PMBR VE time series showed similar peak amplitude & latency across hemispheres. However, individual TFRs revealed variability, including absent contralateral ERD, or even reversed lateralisation of PMBR/ERD. While intra-individual MEG response consistency is well-characterised (e.g. Espenhahn et al., 2017), variability across individuals—especially in ipsilateral responses—remains underexplored. ECoG recordings show fMRI visual cortex NBR is associated with an absence of high frequency band responses (Fracasso et al, 2022) whilst rodent optical imaging spectroscopy studies indicate gamma-band power reductions related to negative hemodynamic responses (Boorman et al, 2015). However, we found no definitive differences in oscillatory activity, including motor-gamma, within ipsilateral hemisphere suggestive of mechanisms which may underpin NBR.
Abstract:
Human behaviour relies on collaborative and antagonistic brain activity. In unilateral sensorimotor tasks, fMRI reveals positive and negative BOLD responses (PBR/NBR) in the contralateral and ipsilateral sensory cortices respectively (Nelson & Mayhew, 2024), but their neural basis remains poorly understood. We used MEG to examine broadband oscillatory responses during unilateral motor tasks, to identify contralateral and ipsilateral signatures that might underlie PBR and NBR. Most previous studies focus on the positive motor BOLD component (e.g. Stevenson et al., 2011), overlooking potential ipsilateral contributions. We analysed a subset of the MEGUK dataset (35 adults recruited from Aston University). Participants performed right-hand finger abductions following visual grating offset (1.5–2s duration; 8s inter-trial interval). MEG & EMG data were processed with MNE-Python (v1.8.0) using the MNE-BIDs pipeline. Source activity was reconstructed in the primary motor cortex (M1) via LCMV beamforming, using Freesurfer-derived anatomical models. Analyses targeted three time–frequency windows: (i) beta (15–30 Hz) ERD (event-related desynchronisation; −500–500 ms), (ii) PMBR (post-movement beta rebound; 1000–2000 ms), and (iii) gamma (60–90 Hz) ERS (event-related synchronisation; −500–500 ms), all time-locked to EMG peak onset. Peak source activity was localised within contralateral & ipsilateral precentral gyri, defining M1 regions of interest (ROIs) resulting in 6 virtual electrode (VE) locations per participant. Group-level TFRs (via DPSS multitapers) showed bilateral ERD & PMBR, but with stronger contralateral dominance. PMBR VE time series showed similar peak amplitude & latency across hemispheres. However, individual TFRs revealed variability, including absent contralateral ERD, or even reversed lateralisation of PMBR/ERD. While intra-individual MEG response consistency is well-characterised (e.g. Espenhahn et al., 2017), variability across individuals—especially in ipsilateral responses—remains underexplored. ECoG recordings show fMRI visual cortex NBR is associated with an absence of high frequency band responses (Fracasso et al, 2022) whilst rodent optical imaging spectroscopy studies indicate gamma-band power reductions related to negative hemodynamic responses (Boorman et al, 2015). However, we found no definitive differences in oscillatory activity, including motor-gamma, within ipsilateral hemisphere suggestive of mechanisms which may underpin NBR.
15:45 – 16:15
Tea break
Ground Floor
Ground Floor
Oscillations and rhythmic MEG
16:15 – 16:45
Long talk
Long talk
Multi-sensory rhythmic stimulation of hippocampal theta to modulate episodic memory in humans
Eleonora Marcantoni
University of Glasgow
Eleonora Marcantoni
University of Glasgow
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Co-authors: Eleonora Marcantoni , Danying Wang, Robin Ince, Dan Bush, Lauri Parkkonen, Satu Palva, Simon Hanslmayr
Abstract:
Hippocampal theta oscillations play a critical role in binding multisensory information into coherent episodic memories. Recent evidence suggests that externally entraining these oscillations via 4-Hz audio-visual Rhythmic Sensory Stimulation (RSS) can significantly enhance memory performance in associative memory tasks. However, the current “one-size-fits-all†stimulation approach overlooks individual differences in neural dynamics, potentially contributing to the variability observed in behavioral outcomes. To address this limitation, we developed a pipeline to estimate the individual’s hippocampal theta frequency during a memory task and adapt the stimulation frequency in real time. The pipeline comprises several key steps. First, hippocampal signals are extracted from MEG recordings using an LCMV beamformer. Next, Generalized Eigenvalue Decomposition (GED) is applied to isolate theta-band activity from the broadband signal. Finally, the Cyclic Homogeneous Oscillation (CHO) detection method is used to verify the presence of oscillations and identify their central frequency. This frequency is then used to dynamically adjust the flickering rate of the sensory stimuli during the task. As a proof of concept, we first validated the use of GED and CHO on rodent LFP data by attempting to replicate the well-established correlation between running speed and hippocampal theta frequency. The results confirmed the feasibility of this approach, with the pipeline successfully reproducing the expected relationship (R = 0.27, p < .001). Subsequently, we applied the full pipeline offline to a human MEG dataset collected during an associative memory task involving 4-Hz RSS. Our aim was to evaluate whether the pipeline could detect stimulation-induced changes in hippocampal theta frequency. As hypothesized, the estimated frequencies during stimulation were significantly closer to 4 Hz compared to pre- and post-stimulation windows (main effect of time: F(6,120) = 24.99, p < .001, η² = 0.315). Currently, we are validating the pipeline using a simultaneous MEG-iEEG dataset, allowing us to compare the frequencies estimated from MEG with ground-truth hippocampal activity recorded via iEEG. This step will offer critical insights into the accuracy and reliability of the approach. Preliminary results indicate that real-time detection and tracking of individual theta frequencies is feasible, supporting the potential to test personalised RSS in memory enhancement.
Abstract:
Hippocampal theta oscillations play a critical role in binding multisensory information into coherent episodic memories. Recent evidence suggests that externally entraining these oscillations via 4-Hz audio-visual Rhythmic Sensory Stimulation (RSS) can significantly enhance memory performance in associative memory tasks. However, the current “one-size-fits-all†stimulation approach overlooks individual differences in neural dynamics, potentially contributing to the variability observed in behavioral outcomes. To address this limitation, we developed a pipeline to estimate the individual’s hippocampal theta frequency during a memory task and adapt the stimulation frequency in real time. The pipeline comprises several key steps. First, hippocampal signals are extracted from MEG recordings using an LCMV beamformer. Next, Generalized Eigenvalue Decomposition (GED) is applied to isolate theta-band activity from the broadband signal. Finally, the Cyclic Homogeneous Oscillation (CHO) detection method is used to verify the presence of oscillations and identify their central frequency. This frequency is then used to dynamically adjust the flickering rate of the sensory stimuli during the task. As a proof of concept, we first validated the use of GED and CHO on rodent LFP data by attempting to replicate the well-established correlation between running speed and hippocampal theta frequency. The results confirmed the feasibility of this approach, with the pipeline successfully reproducing the expected relationship (R = 0.27, p < .001). Subsequently, we applied the full pipeline offline to a human MEG dataset collected during an associative memory task involving 4-Hz RSS. Our aim was to evaluate whether the pipeline could detect stimulation-induced changes in hippocampal theta frequency. As hypothesized, the estimated frequencies during stimulation were significantly closer to 4 Hz compared to pre- and post-stimulation windows (main effect of time: F(6,120) = 24.99, p < .001, η² = 0.315). Currently, we are validating the pipeline using a simultaneous MEG-iEEG dataset, allowing us to compare the frequencies estimated from MEG with ground-truth hippocampal activity recorded via iEEG. This step will offer critical insights into the accuracy and reliability of the approach. Preliminary results indicate that real-time detection and tracking of individual theta frequencies is feasible, supporting the potential to test personalised RSS in memory enhancement.
Oscillations and rhythmic MEG
16:45 – 17:00
Short talk
Short talk
Subcortical Contributions to Oscillatory and Behavioural Asymmetries: Insights from the Hemispheric Laterality of Basal Ganglia and Thalamus
Tara Ghafari
University of Oxford
Tara Ghafari
University of Oxford
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Co-authors: Tara Ghafari, Mohammad Ebrahim Katebi, Mohammad Hossein Ghafari, Aliza Finch, Ole Jensen
Abstract:
Healthy individuals exhibit a subtle leftward attentional bias known as pseudoneglect, typically attributed to right-hemisphere dominance for attention. While cortical contributions are well-established, the role of subcortical structures remains less clear. In this study, we explored how naturally occurring volumetric asymmetries in subcortical regions relate to both behavioural and neurophysiological markers in healthy adults. In a behavioural experiment with 44 participants, we assessed spatial bias using a computerised landmark task and eye-tracking, quantifying the point of subjective equality (PSE). Structural T1-weighted MRI data were processed using FSL FIRST to calculate lateralised volumes (LVs) of seven subcortical structures. General linear model analyses revealed that individual differences in PSE were significantly predicted by the lateralised volume of the putamen, suggesting a subcortical origin for individual variation in attentional bias. Complementing this, we analysed resting-state MEG data from a larger cohort (n = 590, Cam-CAN dataset), correlating frequency-specific hemispheric power asymmetries with subcortical volume asymmetries. We found significant associations between the lateralisation of oscillatory power and subcortical volumes. Notably, the putamen showed correlations with lateralised power in the beta band, the thalamus was significantly correlated with alpha laterality and the hippocampus with laterality in the delta/theta bands. Together, these findings provide converging evidence that subcortical volumetric asymmetries not only shape behavioural hemifield biases in spatial attention but also influence the lateralisation of neocortical oscillatory activity. This work highlights the importance of subcortical structures in supporting attentional processes in the healthy brain and lays the groundwork for future research into their role in neurodegenerative disorders.
Abstract:
Healthy individuals exhibit a subtle leftward attentional bias known as pseudoneglect, typically attributed to right-hemisphere dominance for attention. While cortical contributions are well-established, the role of subcortical structures remains less clear. In this study, we explored how naturally occurring volumetric asymmetries in subcortical regions relate to both behavioural and neurophysiological markers in healthy adults. In a behavioural experiment with 44 participants, we assessed spatial bias using a computerised landmark task and eye-tracking, quantifying the point of subjective equality (PSE). Structural T1-weighted MRI data were processed using FSL FIRST to calculate lateralised volumes (LVs) of seven subcortical structures. General linear model analyses revealed that individual differences in PSE were significantly predicted by the lateralised volume of the putamen, suggesting a subcortical origin for individual variation in attentional bias. Complementing this, we analysed resting-state MEG data from a larger cohort (n = 590, Cam-CAN dataset), correlating frequency-specific hemispheric power asymmetries with subcortical volume asymmetries. We found significant associations between the lateralisation of oscillatory power and subcortical volumes. Notably, the putamen showed correlations with lateralised power in the beta band, the thalamus was significantly correlated with alpha laterality and the hippocampus with laterality in the delta/theta bands. Together, these findings provide converging evidence that subcortical volumetric asymmetries not only shape behavioural hemifield biases in spatial attention but also influence the lateralisation of neocortical oscillatory activity. This work highlights the importance of subcortical structures in supporting attentional processes in the healthy brain and lays the groundwork for future research into their role in neurodegenerative disorders.
Oscillations and rhythmic MEG
17:00 – 17:15
Short talk
Short talk
Neuronal correlates of predictive distractor suppression
Oscar Ferrante
University of Birmingham
Oscar Ferrante
University of Birmingham
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Co-authors: Ole Jensen, Clayton Hickey
Abstract:
Visual attention is influenced by the statistical regularities of our environment, with spatially predictable distractors being actively suppressed. Yet, the neural mechanisms underlying this suppression remain poorly understood. In this talk, I will show how we have used magnetoencephalography (MEG), rapid invisible frequency tagging (RIFT), and multivariate decoding analysis to provide new insight on the processing of predicted distractor locations in the human brain. Using a statistical learning visual search task where a colour-singleton distractor appeared more frequently on one side of the visual field, we found that early visual cortex exhibited reduced neural excitability in the pre-search interval at retinotopic sites corresponding to higher distractor probabilities. During this period, a temporo-occipital network encoded these distractor locations, supporting the hypothesis that proactive suppression directs visual attention away from predictable distractors. Notably, the neural activity associated with pre-search distractor processing extended into the post-search period during late attentional stages (around 200 ms), suggesting a mechanistic link between proactive and reactive distractor suppression. These findings offer critical insights into the neuronal correlates of predictive distractor suppression and provide a deeper understanding of the cognitive mechanisms underlying selective attention.
Abstract:
Visual attention is influenced by the statistical regularities of our environment, with spatially predictable distractors being actively suppressed. Yet, the neural mechanisms underlying this suppression remain poorly understood. In this talk, I will show how we have used magnetoencephalography (MEG), rapid invisible frequency tagging (RIFT), and multivariate decoding analysis to provide new insight on the processing of predicted distractor locations in the human brain. Using a statistical learning visual search task where a colour-singleton distractor appeared more frequently on one side of the visual field, we found that early visual cortex exhibited reduced neural excitability in the pre-search interval at retinotopic sites corresponding to higher distractor probabilities. During this period, a temporo-occipital network encoded these distractor locations, supporting the hypothesis that proactive suppression directs visual attention away from predictable distractors. Notably, the neural activity associated with pre-search distractor processing extended into the post-search period during late attentional stages (around 200 ms), suggesting a mechanistic link between proactive and reactive distractor suppression. These findings offer critical insights into the neuronal correlates of predictive distractor suppression and provide a deeper understanding of the cognitive mechanisms underlying selective attention.
Oscillations and rhythmic MEG
17:15 – 17:30
Short talk
Short talk
Pre-stimulus shape predictions fluctuate at alpha rhythms and bias subsequent perception
Dorottya Hetenyi
University College London
Dorottya Hetenyi
University College London
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Co-authors: Dorottya Hetenyi & Peter Kok
Abstract:
Predictions about future events significantly influence how we process sensory signals. In previous work, we demonstrated that predicted shape representations exhibit oscillatory activity in the alpha band (10–11 Hz) during pre-stimulus intervals. In that study, participants performed a task that was orthogonal to the shape predictions. Here, we extended these findings by having participants perform a shape identification task that directly relied on the shape predictions, allowing us to link the neural correlates of prediction to subjective perception. We used magnetoencephalography (MEG) combined with multivariate decoding to examine the content and frequency characteristics of perceptual predictions and relate them to behaviour. The shape identification task involved auditory cues predicting which shape was likely to appear. To make the identification of the shapes challenging, they were embedded in white noise. First, we found that valid prediction cues improved both identification accuracy and reaction times. Signal detection theory analyses revealed that participants were significantly biased toward reporting the predicted shape (i.e., reduced criterion), without a change in sensitivity (i.e., similar d-prime). We replicated our previous finding that predicted shape representations fluctuate in the alpha band (10–11 Hz). Logistic regression analyses further revealed that this shape-specific alpha power predicted perceptual biases induced by the predictions. That is, when shape-specific alpha power was high, participants were more likely to perceive the predicted shape. In contrast, higher raw sensor-level occipital alpha power was associated with a greater likelihood of reporting the unpredicted shape. These results suggest that content-specific alpha fluctuations and general occipital alpha power serve distinct functions in visual perception. Taken together, our findings demonstrate that sensory predictions are represented in pre-stimulus alpha oscillations and that these oscillatory signals shape how we perceive the world.
Abstract:
Predictions about future events significantly influence how we process sensory signals. In previous work, we demonstrated that predicted shape representations exhibit oscillatory activity in the alpha band (10–11 Hz) during pre-stimulus intervals. In that study, participants performed a task that was orthogonal to the shape predictions. Here, we extended these findings by having participants perform a shape identification task that directly relied on the shape predictions, allowing us to link the neural correlates of prediction to subjective perception. We used magnetoencephalography (MEG) combined with multivariate decoding to examine the content and frequency characteristics of perceptual predictions and relate them to behaviour. The shape identification task involved auditory cues predicting which shape was likely to appear. To make the identification of the shapes challenging, they were embedded in white noise. First, we found that valid prediction cues improved both identification accuracy and reaction times. Signal detection theory analyses revealed that participants were significantly biased toward reporting the predicted shape (i.e., reduced criterion), without a change in sensitivity (i.e., similar d-prime). We replicated our previous finding that predicted shape representations fluctuate in the alpha band (10–11 Hz). Logistic regression analyses further revealed that this shape-specific alpha power predicted perceptual biases induced by the predictions. That is, when shape-specific alpha power was high, participants were more likely to perceive the predicted shape. In contrast, higher raw sensor-level occipital alpha power was associated with a greater likelihood of reporting the unpredicted shape. These results suggest that content-specific alpha fluctuations and general occipital alpha power serve distinct functions in visual perception. Taken together, our findings demonstrate that sensory predictions are represented in pre-stimulus alpha oscillations and that these oscillatory signals shape how we perceive the world.
Oscillations and rhythmic MEG
17:30 – 17:45
Short talk
Short talk
Human Hippocampal Theta-Gamma Coupling Coordinates Sequential Planning During Navigation
Zimo Huang
University College London
Zimo Huang
University College London
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Co-authors: James Bisby, Neil Burgess, Daniel Bush
Abstract:
Human behaviour often relies on executing a specific sequence of actions to achieve a desired outcome. However, the neural mechanisms underlying the dynamic construction and maintenance of such sequences during goal-directed behaviour are not yet clear. Empirical and theoretical studies of working memory function suggest that sequential information may be encoded in neural circuits by bursts of gamma activity occurring at consecutive theta phases. Here, we asked whether similar coding schemes might support sequential planning during goal-directed navigation. Using non-invasive magnetoencephalography and an abstract navigation task, we found that hippocampal theta power during both planning and subsequent navigation decreased with proximity to the current goal, only during accurate navigation. At the same time, theta-gamma phase-amplitude coupling increased with goal proximity, consistent with sequences of upcoming locations being represented by gamma bursts occurring at successive theta phases. Importantly, entorhinal high gamma and hippocampal low gamma dominated while traversing novel and previously experienced paths, respectively, consistent with previous rodent studies. These findings suggest that hippocampal theta-gamma phase amplitude coupling flexibly and dynamically coordinates sequences of actions during goal-directed behaviour across mammalian species, using different gamma bands for mnemonic and prospective planning.
Abstract:
Human behaviour often relies on executing a specific sequence of actions to achieve a desired outcome. However, the neural mechanisms underlying the dynamic construction and maintenance of such sequences during goal-directed behaviour are not yet clear. Empirical and theoretical studies of working memory function suggest that sequential information may be encoded in neural circuits by bursts of gamma activity occurring at consecutive theta phases. Here, we asked whether similar coding schemes might support sequential planning during goal-directed navigation. Using non-invasive magnetoencephalography and an abstract navigation task, we found that hippocampal theta power during both planning and subsequent navigation decreased with proximity to the current goal, only during accurate navigation. At the same time, theta-gamma phase-amplitude coupling increased with goal proximity, consistent with sequences of upcoming locations being represented by gamma bursts occurring at successive theta phases. Importantly, entorhinal high gamma and hippocampal low gamma dominated while traversing novel and previously experienced paths, respectively, consistent with previous rodent studies. These findings suggest that hippocampal theta-gamma phase amplitude coupling flexibly and dynamically coordinates sequences of actions during goal-directed behaviour across mammalian species, using different gamma bands for mnemonic and prospective planning.
19:00 – 22:00
Social evening with drinks and buffet
Coin Laundry, EC1R 4QP
Coin Laundry, EC1R 4QP
Session | Time | Details |
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09:00 – 09:50 | Coffee Break Ground Floor | |
09:50 – 10:00 | Opening remarks Yulia Bezsudnova, Gareth Barnes University College London | |
Methods for MEG | 10:00 – 10:15 Short talk | MEG measures of target engagement in early-phase clinical trials: Modulation of task and resting-state oscillatory dynamics by a novel AMPAR PAM Krish Singh Cardiff University More details Less details
Co-authors: Krish D Singh, Rasha Hyder, John R. Atack, Simon E. Ward, Jennifer B. Swettenham, Natalie Jones and Neil A Harrison
Abstract: Development of novel pharmacological treatments for neurological and neuropsychiatric disorders is notoriously costly and difficult, with multiple decision-points at which the compound can fail. A critical factor is a lack of evidence that having crossed the blood-brain barrier, the drug engages with the neural target in humans in a way predicted by the pre-clinical evidence. As highlighted by the NIH Fast-Fail Trials (FAST) Initiative, CNS drug discovery could be substantially de-risked, with significant cost and time savings if non-invasive technology could be used to index human target-engagement in early phase clinical trials. MEG is ideal for this because of its enhanced spatial resolution, compared to EEG, and its direct sensitivity to post-synaptic potentials, unlike fMRI. However, MEG is not commonly used. Here, we present results of a novel approach to first-in-human Phase-1 clinical trials where we incorporated two separate MEG evaluations of target engagement in a new compound designed to increase AMPAR activity within the brain, with potential therapeutic indications across several neuropsychiatric disorders. MEG demonstrated that this novel drug modulated resting-state oscillatory activity within multiple brain regions consistent with the known distribution of AMPA receptors across the brain. The most widespread effects were found in the beta and gamma frequency ranges. The AMPAR-PAM also potentiated the 40Hz auditory steady-state response (ASSR) and enhanced cortical responses during a visual task. No effects were detected in a multi-deviant mis-matched negativity paradigm. The size of these drug-induced changes varied in a dose-dependent way and/or were correlated with individual blood assays of drug exposure at the time of MEG scanning. This study provides proof-of-concept for how drug-development scientists, MEG neuroimaging experts, clinicians, clinical-trials organisations and commercial pharma companies can collaborate to simultaneously and efficiently test compound target-engagement, pharmacodynamics and safety in a Phase-I clinical trial. We believe that wider scale adoption of this approach would significantly de-risk and accelerate the CNS drug-development process and increase the chance of successful treatments being available to patients. Because of MEGUKI’s high-quality research and highly integrated collaborative nature, we are in an excellent position to become international leaders in this exciting new innovation area. |
Methods for MEG | 10:15 – 10:30 Short talk | Modulation of auditory system neuroplasticity by a novel AMPAR PAM drug: Evidence from MEG Rasha Hyder Cardiff University More details Less details
Co-authors: Rasha Hyder, John R. Atack, Simon E. Ward, Jennifer B. Swettenham, Natalie Jones, Luke Tait, Neil A Harrison and Krish D Singh
Abstract: The sensitivity of classical auditory measures such as auditory steady state response (ASSR) and auditory mismatch negativity (MMN) to pharmacological interventions has been confirmed both in human and animal research. Here, as part of a first-in-human Phase I clinical trial, we used pharmaco-MEG to assess the functional effects of target engagement of a novel positive allosteric modulator (PAM) of AMPA receptors developed at Cardiff University. This drug enhances AMPAR function in a use-dependent manner thereby impacting synaptic plasticity and overall brain health. This was a within-subject, placebo-controlled, double-blind crossover study during which we acquired MEG data during 40 Hz-steady-state auditory response task and auditory multi-feature MMN paradigm from 19 healthy volunteers. In each of 3 separate visits, participants received a single dose of placebo, low- or high-dose of the drug. MEG recording started an hour post-dose. In addition to MEG, we collected structural MRI scans of participants. All participants showed clear ASSR and MMN responses both in sensor and source-space in all three sessions. While no drug effects were found in the auditory MMN task, a clear enhancement in the 40Hz ASSR evoked power was seen in the right hemisphere with the high-dose. To better understand the mechanistic functioning of the drug and explain the enhancement in ASSR in the right hemisphere with the high dose only, we are currently analysing the 40Hz data using dynamic causal modelling (DCM), based on an optimised thalamo-cortical microcircuit model, with channel-specific conductance. Findings from this study provide further evidence for the potential of MEG-based neurophysiological measures, in particular ASSR, as novel translational biomarkers for indexing target engagement and de-risking CNS drug-development. |
Methods for MEG | 10:30 – 10:45 Short talk | Do we still need resting-state MEG? Lainya Knopik Cardiff University More details Less details
Co-authors: Krish Singh, Luke Tait, Carolyn McNabb
Abstract: Resting-state paradigms have become ubiquitous in brain activity/connectivity studies of function in both health and disease, with MEG able to probe resting oscillatory dynamics in multiple frequency bands to reveal static/dynamic networks at the millisecond level. Yet, during rest, the cognitive state of participants is uncontrolled/unknown, yielding unwanted variance and potential group-level differences. In addition, when task paradigms are also used, resting-state paradigms significantly add to the scan time burden – this is especially problematic for challenging patient populations and young children. To address this, we examined whether static functional connectivity (FC) patterns derived from a visual task recording could reproduce those observed during rest, eliminating the need for a specific resting-state recording. Using MEG from 166 participants, leakage-corrected amplitude envelope correlations were calculated, yielding frequency-specific static connectivity maps for each person. This was done for both a resting-state recording and a visual-gamma recording i.e. in the latter the presence of the task was ignored during analysis. Connectivity maps, and sub-networks generated by hierarchical clustering, were compared across the two datasets using inter-session correlation. We also found a significant correlation between resting-state MEG connectivity and age and explored whether this was reproduced in the maps derived from the visual gamma data. Preliminary findings reveal moderate inter-session correlations (mean r = 0.56) in the beta-band (13-30 Hz) between FC matrices. Hierarchical clustering identified 26 stable sub-networks with significant cross-session correlations (r = 0.50–0.71, p < .001). We also observed highly reproducible age-related connectivity patterns in the alpha band (8-13 Hz) across both rest and task data (r = 0.84, p < .001). This work challenges the convention that resting-state MEG is uniquely suited for capturing connectivity and shows that task MEG data can reveal the same core features of intrinsic brain architecture, potentially substituting for rest in contexts where time, cost, or participant compliance is limited. This offers an efficient, pragmatic and powerful approach, streamlining MEG protocols and enhancing accessibility, especially in clinical or developmental populations. Future work will extend this analysis to study state-dynamics, activity, peak frequency, other tasks and clinical populations. |
Methods for MEG | 10:45 – 11:00 Short talk | Multi-Scale Brain Dynamics in M/EEG with Time-Delay Embedded Hidden Markov Models Fabrice Guibert Ecole Polytechnique Fédérale de Lausanne (EPFL); University of Geneva (UNIGE) More details Less details
Co-authors: Fabrice Guibert, Jeroen Van Schependom, Chiara Rossi, Dimitri Van de Ville, Daphné Bavelier
Abstract: M/EEG studies have successfully described brain activity through the succession of different states. In the context of the time-delay embedding (TDE)-hidden Markov models (HMM) methodology, these spatiotemporal states have both spatial and oscillatory properties. TDE-HMM states reflect changes in spatio-temporal covariance structures. Yet, despite the well-accepted view that the brain functions at multiple temporal scales, current analyses have primarily focused on the trial level. Objective. We aim to investigate how TDE-HMM-state time courses behave across different temporal scales. Methods. We use cryogenic MEG data collected at two sites (Brussels, N=38; Nottingham, N=8-replication data set). Each task is structured in blocks of either 0-back, 1-back, or 2-back,  interleaved in pseudo-random order, and separated by periods of instruction, as well as rest – thus providing a rich higher-order block structure. Following standard MEG preprocessing steps, we train a TDE-HMM model and extract state probability time courses. To investigate whether we can extract dynamics at multiple temporal scales, we first ask if probability time courses can be used to retrieve task-related conditions at the block level, such as being on-task versus off-task, N-back blocks of differing difficulty, and ordering effects of blocks. We then verify if probability time courses can also be used to contrast task-related conditions at the trial level i.e. hits against correct rejects. Importantly, these evaluations are conducted multiple window sizes in the TDE step of the HMM, and evaluate discriminability. Stability is assessed using multiple restarts. Results. We find that states exhibit a rich structure at the trial level, consistent with previous studies. We also demonstrate that states capture block-level structure, such that state activations distinguish between being on- and off-task, being in different N-back difficulty blocks, as well as ordering effects on N-back blocks. Thus, state time courses show striking temporal structure, yet also capture finer patterns at the trial level. Our results are stable across model restarts. Finally, we also demonstrate the influence of window size, as well as a phase transition in state power spectrum for window sizes longer than 80 ms. Conclusion. This study suggests that brain state dynamics should be considered not only at the trial level in M/EEG data, but also at a coarser level to unveil a greater range of temporal dynamics. |
11:00 – 11:30 | Tea break Mary Ward Hall | |
Deep Learning | 11:30 – 11:45 Short talk | Ephys-GPT: A foundation model for electrophysiological data Rukuang Huang University of Oxford More details Less details
Co-authors: Sungjun Cho, Mark Woolrich
Abstract: Foundation models have demonstrated remarkable success across different domains by leveraging large-scale, unlabelled datasets and self-supervised learning to extract rich, transferable representations. For electrophysiological data, however, existing models are predominantly trained on transformed versions of the data in the time-frequency domain (e.g. with Fourier or wavelet transforms), which may compromise the temporal and frequency resolution and relies on pre-defined hyper-parameters of the transformations. We introduce Ephys-GPT, a foundation model pre-trained on large amount of raw resting-state magnetoencephalography (MEG) recordings. Inspired by the autoregressive objectives of the GPT models, Ephys-GPT is trained on tokenised raw data with a bespoke tokeniser to predict future tokens. We show that Ephys-GPT generates realistic neural recordings that preserves key statistical and physiological properties, including power spectral density, spatial patterns of frequency bands, between-subject variability, and importantly, oscillatory bursting dynamics (e.g. beta bursts in the motor cortex). Furthermore, the model can be efficiently fine-tuned on limited task-evoked data. Generated data from the fine-tuned model shows time-locked task responses to surrogate task event sequences. This work demonstrates the feasibility and potential of large-scale, self-supervised foundation models on raw electrophysiological signals, paving the way for powerful general-purpose, multi-modal tools in neural decoding and computational neuroscience. |
Deep Learning | 11:45 – 12:00 Short talk | Learnable Sample-Level Tokenisation for MEG Foundation Models Sungjun Cho University of Oxford More details Less details
Co-authors: Rukuang Huang, Oiwi Parker Jones, Mark W Woolrich
Abstract: Recent advancements in large language models have catalysed the development of transformer-based foundation models for MEG and other neuroimaging modalities, aiming to extract generalisable patterns from large datasets that can be flexibly adapted to various modalities and clinical disorders with minimal retraining. This endeavour in turn necessitated efficient tokenisation strategies that can compactly summarise neural data into transformer-compatible representations. Until now, existing tokenisers primarily adapted techniques designed for general, non-biological time-series data, such as patching, time-frequency transformations, or vector quantisation. However, these often sacrifice temporal resolution, limiting interpretability and precise temporal alignment essential for MEG data analyses. While some tokenisers do preserve temporal fidelity (e.g., mu-transform tokenisation), they are not data-adaptive and may poorly capture temporal dependencies and latent structures in MEG signals. To address these limitations, we propose a new learnable tokeniser that models tokens using convolution kernels. These kernels are simultaneously learnt and fit to the MEG data using a recurrent neural network (RNN). Crucially, this maintains full temporal resolution (i.e., a sample-level tokenisation) and enables a tokeniser to model causal structure in sequential data. We evaluated our method through a signal reconstruction task, benchmarking its performance against traditional non-learnable approaches. Our tokeniser achieved a strong reconstruction accuracy, explaining over 97% of the variance in both simulated and real resting-state MEG data, while also accounting for subject-level variability. Furthermore, it required significantly fewer tokens (90-120) than the conventional mu-transform method (256 tokens) and generalised robustly across datasets and MEG scanner types. When a transformer model was trained on the derived tokens, it achieved higher token prediction accuracy with our tokeniser, explaining more variance in the original signals. In conclusion, we present the first data-adaptive, sample-level tokenisation framework based on convolution kernels and RNN-based inference, capable of capturing fine-grained temporal dynamics suitable for transformer-based MEG foundation models. This method offers enhanced temporal resolution and prediction accuracy over existing approaches and holds promise for facilitating more reliable foundation models in neuroimaging. |
12:00 – 12:30 Flash talks | Session 2 flash talks Mary Ward Hall | |
12:30 – 14:00 | Lunch and poster session 2 Ground Floor | |
Clinical Neuroscience | 14:00 – 14:30 Long talk | MEG in Psychosis: individual differences in neural oscillations underlying language disorganization and impoverishment Hsi (Tiana) Wei McGill University; Douglas Mental Health Institute More details Less details
Co-authors: Hsi (Tiana) Wei, Dominic Boutet, Rukun Dou, Jessica Ahrens, Nadia Zeramdini, Alban Voppel, Fernando Miguel Gonzales Aste, Sylvain Baillet, Lena Palaniyappan
Abstract: Schizophrenia is characterized by incoherent speech and reduced linguistic output, associated with neural dysconnectivity and aberrant oscillatory activity. However, the relationship between these neuronal changes and communication deficits remains unclear. This project explores the hypothesis that neuronal dysfunction underlies language disorganization and impoverishment by investigating associations between neuronal oscillations during visuo-audio integration and language features derived via automated processing pipelines in individuals with and without psychosis. Twenty-five patients with schizophrenia and 25 healthy controls completed symptom and speech assessments, Magnetoencephalography (MEG) during an audiovisual task and resting state and structural MRI. MEG recordings were obtained during an audiovisual simultaneity judgment task and open-eye resting. MEG data were source-localized to each participant’s normalized structural MRI, preprocessed, and epoched to motor responses and sensory stimuli to assess event-related power modulations. Speech data collected during interviews were analyzed for acoustic/linguistic features using Python. Preliminary analyses of 16 controls (Age M=31.81, SD=9.59) and 13 schizophrenia (SZ) patients (Age M=34.46, SD=9.38) revealed attenuated post-movement beta rebound (PMBR) in patients, bilaterally in frontal regions. Reduced PMBR likely suggests diminished interhemispheric beta-mediated functional inhibition. Notably, weaker PMBR correlated with hallucinatory behavior (r(27)=-.38, p=0.04) and blunted affect (r(27)=-.38, p=0.04) on the PANSS. Speech analysis showed that apathetic social withdrawal was linked to fewer syllables (r(27)=-.41, p=0.03) and unnatural mannerisms and postures on PANSS related with reduced syllables (r(27)=-.51, p<0.01), phonation time (r(27)=-.48, p<0.01), and pauses (r(27)=-.38, p=0.04). Stronger PMBR in the frontal region correlated with greater syllable production (r(27)=.37, p<0.05). These findings highlight associations between beta-band power, clinical symptoms, and speech performance, with PMBR strongest in controls, followed by more verbal patients, and weakest in less verbal patients. Upcoming analyses will include personalized spectral power characteristics, bilateral frontotemporal oscillatory connectivity. With a more comprehensive sample size and analysis, this project aims to elucidate individual differences linking neuronal oscillations to language symptoms in psychosis. |
Clinical Neuroscience | 14:30 – 14:45 Short talk | Weakened prefrontal activation dynamics associated with slowed information processing speed in multiple sclerosis Olivier Burta Vrije Universiteit Brussel More details Less details
Co-authors: Fahimeh Akbarian, Chiara Rossi, Diego Vidaurre, Marie Bie D’hooghe, Miguel D’Haeseleer, Guy Nagels, Jeroen Van Schependom
Abstract: Information processing speed (IPS) is a core cognitive deficit in people with multiple sclerosis (PwMS). Previous efforts have associated IPS performance to frontal regions, but were constrained by limited temporal resolution. In this work, we employed a data-driven method, the time delay embedded-hidden Markov model (TDE-HMM), to identify task-specific states that are spectrally defined with distinct temporal and spatial profiles. We used magnetoencephalographic (MEG) data recorded while healthy controls and PwMS performed a cognitive task designed to capture IPS, the Symbol Digit Modalities Test (SDMT). The TDE-HMM identified five task-relevant states, supporting a tri-factor contribution to IPS: sensory speed (occipital visual detection and processing), cognitive speed (prefrontal executive and frontoparietal attention shift), and motor speed (sensorimotor). We observed reduced prefrontal and increased frontoparietal activation in PwMS, which significantly correlated with offline SDMT performance. This work can drive future research for MS treatments targeting IPS improvements. |
Clinical Neuroscience | 14:45 – 15:00 Short talk | Varying patterns of association between cortical large-scale networks and subthalamic nucleus activity in Parkinson’s Disease Oliver Kohl Heinrich-Heine-University Düsseldorf More details Less details
Co-authors: Chetan Gohil, Matthias Sure, Alfons Schnitzler, Esther Florin
Abstract: Parkinson’s Disease (PD) is characterised by the progressive degeneration of dopaminergic neurons and the accumulation of Lewy bodies in the substantia nigra pars compacta. This pathology disrupts dopaminergic regulation of the basal ganglia, leading to motor impairments. While basal ganglia activity is known to synchronise with specific cortical regions, the broader dynamics of cortical network involvement remain unclear. To investigate this, we analysed simultaneous magnetoencephalography (MEG) and subthalamic nucleus (STN) local field potential (LFP) recordings from 25 individuals with PD, both on and off dopaminergic medication. We identified dynamic large-scale cortical networks with a Time-Delay Embedded Hidden Markov Model that showed distinct patterns of STN-cortical coherence. Notably, increased synchrony between the STN and supplementary motor area (SMA) occurred during activation of a sensorimotor network and a network characterised by widespread cortical power increases. The sensorimotor network was associated with elevated STN 9.5 to 23-Hz power and beta bursts, while the widespread activation network was linked to increased STN power in the 5 to 16.5-Hz range. These findings were replicated in a second dataset of 17 additional participants. Interestingly, dopaminergic medication most strongly reduced STN beta power during activation of cortical networks that did not show increased STN-motor cortical coherence. Overall, our results indicate that large-scale cortical networks exhibit STN-cortical communication in distinct ways. The sensorimotor and widespread activation networks, in particular, may serve as spatiotemporal windows into subcortical STN processing. These cortical network signatures in non-invasive recordings may offer a novel avenue for accessing subcortical information relevant to PD, potentially informing diagnosis and treatment strategies. |
Clinical Neuroscience | 15:00 – 15:15 Short talk | Impaired mPFC–hippocampal theta phase coupling during memory retrieval in Schizophrenia Ingrid Martin Kings College London More details Less details
Co-authors: Daniel Bush, Rick Adams, Neil Burgess
Abstract: Theta-band (1-7Hz) oscillations and long-range phase coupling within the hippocampal–medial prefrontal cortex (HPC–mPFC) network are critical for memory function and have been extensively characterized in animal models. However, their role in human cognition and psychiatric disorders such as schizophrenia remains poorly understood. This study used magnetoencephalography (MEG) to investigate theta oscillatory dynamics during an associative inference task in patients with schizophrenia and matched healthy controls. Patients exhibited marked impairments in recognition memory, including elevated false alarm rates, and showed deficits in both direct and inferential memory retrieval. While both groups demonstrated increased mPFC theta power and HPC–mPFC theta coupling during encoding, only healthy controls maintained this coupling at retrieval. In contrast, patients showed a breakdown in theta phase coupling during memory retrieval, pointing to a functional disconnection within the HPC–mPFC network. These findings extend prior rodent models of hippocampal–prefrontal interactions to the human domain and provide novel evidence that schizophrenia is associated with task-specific disruptions in theta synchrony. This suggests a potential neural mechanism underlying relational memory impairments in psychosis, with implications for targeting HPC–PFC network dysfunction in therapeutic interventions. |
Clinical Neuroscience | 15:15 – 15:30 Short talk | High-density full-head on-scalp MEG for Epilepsy Svenja Knappe FieldLine Medical; University of Colorado Boulder More details Less details
Co-authors: Svenja Knappe, Isabelle Buard, K. Jeramy Hughes, Orang Alem, Tyler Maydew, Eugene Kronberg, Peter Teale, Teresa Cheung
Abstract: Optically-pumped magnetometers (OPMs) have been identified as a possible candidate for use in evaluations of patients with epilepsy. We present first results of an ongoing cross-validation study performed in 20 adult patients with drug-resistant focal epilepsy to date. In addition, sensory-evoked activity was recorded and localized in the patients and a set of healthy controls. The goal of the study is to compare the data quality between OPM-based MEG and conventional cryogenic MEG, using simultaneous EEG and MEG recordings. Methods: To assess the OPM data quality, subjects underwent simultaneously EEG and MEG resting-state recordings on a cryogenic MEG system and an on-scalp MEG system for 30 min each. Co-registration with the subject’s anatomy was performed by digitizing the positions of five head-position indicator (HPI) coils with respect to three fiducials and localizing them with the MEG system. The resting data were filtered with a bandpass filter from 3 – 70 Hz or 20 – 70 and a notch filter at 60 Hz. Bad segments containing muscle activity were marked, and a kurtosis was calculated. Thresholds in the volumetric images were used to identify the peak locations of high kurtosis, where virtual channels were computed. Peaks were marked for comparison with the EEG signals and for dipole fits. For the sensory mapping study, auditory, visual, somatosensory, and motor areas were localized both by performing dipole fits and event-related beamformer analysis. Results: Clear interictal spikes were recorded at the same time points and exhibit similar morphology in several patients between the EEG and OPM recordings, consistent with the EEG and cryogenic MEG results. There was also good agreement between the OPM and cryogenic MEG resting data. The results of the sensory study agreed closely between both the OPM and cryogenic MEG recordings and were consistent with results found in literature. Conclusions: Good agreement was found between the on-scalp MEG and the EEG data. The kurtosis beamformer presents a convenient method for localization of interictal activity and agreed well with the dipole fits. The sensory study showed that the OPM HEDscan system localized sensory-evoked fields reliably and yielded similar data quality to cryogenic MEG systems. The results will have to be validated systematically in a larger number of subjects. |
15:30 – 16:00 | Closing and award ceremony Yulia Bezsudnova, Gareth Barnes University College London | |
16:00 – 17:00 | Tea break Ground Floor |
09:00 – 09:50
Coffee Break
Ground Floor
Ground Floor
09:50 – 10:00
Opening remarks
Yulia Bezsudnova, Gareth Barnes
University College London
Yulia Bezsudnova, Gareth Barnes
University College London
Methods for MEG
10:00 – 10:15
Short talk
Short talk
MEG measures of target engagement in early-phase clinical trials: Modulation of task and resting-state oscillatory dynamics by a novel AMPAR PAM
Krish Singh
Cardiff University
Krish Singh
Cardiff University
More details Less details
Co-authors: Krish D Singh, Rasha Hyder, John R. Atack, Simon E. Ward, Jennifer B. Swettenham, Natalie Jones and Neil A Harrison
Abstract:
Development of novel pharmacological treatments for neurological and neuropsychiatric disorders is notoriously costly and difficult, with multiple decision-points at which the compound can fail. A critical factor is a lack of evidence that having crossed the blood-brain barrier, the drug engages with the neural target in humans in a way predicted by the pre-clinical evidence. As highlighted by the NIH Fast-Fail Trials (FAST) Initiative, CNS drug discovery could be substantially de-risked, with significant cost and time savings if non-invasive technology could be used to index human target-engagement in early phase clinical trials. MEG is ideal for this because of its enhanced spatial resolution, compared to EEG, and its direct sensitivity to post-synaptic potentials, unlike fMRI. However, MEG is not commonly used. Here, we present results of a novel approach to first-in-human Phase-1 clinical trials where we incorporated two separate MEG evaluations of target engagement in a new compound designed to increase AMPAR activity within the brain, with potential therapeutic indications across several neuropsychiatric disorders. MEG demonstrated that this novel drug modulated resting-state oscillatory activity within multiple brain regions consistent with the known distribution of AMPA receptors across the brain. The most widespread effects were found in the beta and gamma frequency ranges. The AMPAR-PAM also potentiated the 40Hz auditory steady-state response (ASSR) and enhanced cortical responses during a visual task. No effects were detected in a multi-deviant mis-matched negativity paradigm. The size of these drug-induced changes varied in a dose-dependent way and/or were correlated with individual blood assays of drug exposure at the time of MEG scanning. This study provides proof-of-concept for how drug-development scientists, MEG neuroimaging experts, clinicians, clinical-trials organisations and commercial pharma companies can collaborate to simultaneously and efficiently test compound target-engagement, pharmacodynamics and safety in a Phase-I clinical trial. We believe that wider scale adoption of this approach would significantly de-risk and accelerate the CNS drug-development process and increase the chance of successful treatments being available to patients. Because of MEGUKI’s high-quality research and highly integrated collaborative nature, we are in an excellent position to become international leaders in this exciting new innovation area.
Abstract:
Development of novel pharmacological treatments for neurological and neuropsychiatric disorders is notoriously costly and difficult, with multiple decision-points at which the compound can fail. A critical factor is a lack of evidence that having crossed the blood-brain barrier, the drug engages with the neural target in humans in a way predicted by the pre-clinical evidence. As highlighted by the NIH Fast-Fail Trials (FAST) Initiative, CNS drug discovery could be substantially de-risked, with significant cost and time savings if non-invasive technology could be used to index human target-engagement in early phase clinical trials. MEG is ideal for this because of its enhanced spatial resolution, compared to EEG, and its direct sensitivity to post-synaptic potentials, unlike fMRI. However, MEG is not commonly used. Here, we present results of a novel approach to first-in-human Phase-1 clinical trials where we incorporated two separate MEG evaluations of target engagement in a new compound designed to increase AMPAR activity within the brain, with potential therapeutic indications across several neuropsychiatric disorders. MEG demonstrated that this novel drug modulated resting-state oscillatory activity within multiple brain regions consistent with the known distribution of AMPA receptors across the brain. The most widespread effects were found in the beta and gamma frequency ranges. The AMPAR-PAM also potentiated the 40Hz auditory steady-state response (ASSR) and enhanced cortical responses during a visual task. No effects were detected in a multi-deviant mis-matched negativity paradigm. The size of these drug-induced changes varied in a dose-dependent way and/or were correlated with individual blood assays of drug exposure at the time of MEG scanning. This study provides proof-of-concept for how drug-development scientists, MEG neuroimaging experts, clinicians, clinical-trials organisations and commercial pharma companies can collaborate to simultaneously and efficiently test compound target-engagement, pharmacodynamics and safety in a Phase-I clinical trial. We believe that wider scale adoption of this approach would significantly de-risk and accelerate the CNS drug-development process and increase the chance of successful treatments being available to patients. Because of MEGUKI’s high-quality research and highly integrated collaborative nature, we are in an excellent position to become international leaders in this exciting new innovation area.
Methods for MEG
10:15 – 10:30
Short talk
Short talk
Modulation of auditory system neuroplasticity by a novel AMPAR PAM drug: Evidence from MEG
Rasha Hyder
Cardiff University
Rasha Hyder
Cardiff University
More details Less details
Co-authors: Rasha Hyder, John R. Atack, Simon E. Ward, Jennifer B. Swettenham, Natalie Jones, Luke Tait, Neil A Harrison and Krish D Singh
Abstract:
The sensitivity of classical auditory measures such as auditory steady state response (ASSR) and auditory mismatch negativity (MMN) to pharmacological interventions has been confirmed both in human and animal research. Here, as part of a first-in-human Phase I clinical trial, we used pharmaco-MEG to assess the functional effects of target engagement of a novel positive allosteric modulator (PAM) of AMPA receptors developed at Cardiff University. This drug enhances AMPAR function in a use-dependent manner thereby impacting synaptic plasticity and overall brain health. This was a within-subject, placebo-controlled, double-blind crossover study during which we acquired MEG data during 40 Hz-steady-state auditory response task and auditory multi-feature MMN paradigm from 19 healthy volunteers. In each of 3 separate visits, participants received a single dose of placebo, low- or high-dose of the drug. MEG recording started an hour post-dose. In addition to MEG, we collected structural MRI scans of participants. All participants showed clear ASSR and MMN responses both in sensor and source-space in all three sessions. While no drug effects were found in the auditory MMN task, a clear enhancement in the 40Hz ASSR evoked power was seen in the right hemisphere with the high-dose. To better understand the mechanistic functioning of the drug and explain the enhancement in ASSR in the right hemisphere with the high dose only, we are currently analysing the 40Hz data using dynamic causal modelling (DCM), based on an optimised thalamo-cortical microcircuit model, with channel-specific conductance. Findings from this study provide further evidence for the potential of MEG-based neurophysiological measures, in particular ASSR, as novel translational biomarkers for indexing target engagement and de-risking CNS drug-development.
Abstract:
The sensitivity of classical auditory measures such as auditory steady state response (ASSR) and auditory mismatch negativity (MMN) to pharmacological interventions has been confirmed both in human and animal research. Here, as part of a first-in-human Phase I clinical trial, we used pharmaco-MEG to assess the functional effects of target engagement of a novel positive allosteric modulator (PAM) of AMPA receptors developed at Cardiff University. This drug enhances AMPAR function in a use-dependent manner thereby impacting synaptic plasticity and overall brain health. This was a within-subject, placebo-controlled, double-blind crossover study during which we acquired MEG data during 40 Hz-steady-state auditory response task and auditory multi-feature MMN paradigm from 19 healthy volunteers. In each of 3 separate visits, participants received a single dose of placebo, low- or high-dose of the drug. MEG recording started an hour post-dose. In addition to MEG, we collected structural MRI scans of participants. All participants showed clear ASSR and MMN responses both in sensor and source-space in all three sessions. While no drug effects were found in the auditory MMN task, a clear enhancement in the 40Hz ASSR evoked power was seen in the right hemisphere with the high-dose. To better understand the mechanistic functioning of the drug and explain the enhancement in ASSR in the right hemisphere with the high dose only, we are currently analysing the 40Hz data using dynamic causal modelling (DCM), based on an optimised thalamo-cortical microcircuit model, with channel-specific conductance. Findings from this study provide further evidence for the potential of MEG-based neurophysiological measures, in particular ASSR, as novel translational biomarkers for indexing target engagement and de-risking CNS drug-development.
Methods for MEG
10:30 – 10:45
Short talk
Short talk
Do we still need resting-state MEG?
Lainya Knopik
Cardiff University
Lainya Knopik
Cardiff University
More details Less details
Co-authors: Krish Singh, Luke Tait, Carolyn McNabb
Abstract:
Resting-state paradigms have become ubiquitous in brain activity/connectivity studies of function in both health and disease, with MEG able to probe resting oscillatory dynamics in multiple frequency bands to reveal static/dynamic networks at the millisecond level. Yet, during rest, the cognitive state of participants is uncontrolled/unknown, yielding unwanted variance and potential group-level differences. In addition, when task paradigms are also used, resting-state paradigms significantly add to the scan time burden – this is especially problematic for challenging patient populations and young children. To address this, we examined whether static functional connectivity (FC) patterns derived from a visual task recording could reproduce those observed during rest, eliminating the need for a specific resting-state recording. Using MEG from 166 participants, leakage-corrected amplitude envelope correlations were calculated, yielding frequency-specific static connectivity maps for each person. This was done for both a resting-state recording and a visual-gamma recording i.e. in the latter the presence of the task was ignored during analysis. Connectivity maps, and sub-networks generated by hierarchical clustering, were compared across the two datasets using inter-session correlation. We also found a significant correlation between resting-state MEG connectivity and age and explored whether this was reproduced in the maps derived from the visual gamma data. Preliminary findings reveal moderate inter-session correlations (mean r = 0.56) in the beta-band (13-30 Hz) between FC matrices. Hierarchical clustering identified 26 stable sub-networks with significant cross-session correlations (r = 0.50–0.71, p < .001). We also observed highly reproducible age-related connectivity patterns in the alpha band (8-13 Hz) across both rest and task data (r = 0.84, p < .001). This work challenges the convention that resting-state MEG is uniquely suited for capturing connectivity and shows that task MEG data can reveal the same core features of intrinsic brain architecture, potentially substituting for rest in contexts where time, cost, or participant compliance is limited. This offers an efficient, pragmatic and powerful approach, streamlining MEG protocols and enhancing accessibility, especially in clinical or developmental populations. Future work will extend this analysis to study state-dynamics, activity, peak frequency, other tasks and clinical populations.
Abstract:
Resting-state paradigms have become ubiquitous in brain activity/connectivity studies of function in both health and disease, with MEG able to probe resting oscillatory dynamics in multiple frequency bands to reveal static/dynamic networks at the millisecond level. Yet, during rest, the cognitive state of participants is uncontrolled/unknown, yielding unwanted variance and potential group-level differences. In addition, when task paradigms are also used, resting-state paradigms significantly add to the scan time burden – this is especially problematic for challenging patient populations and young children. To address this, we examined whether static functional connectivity (FC) patterns derived from a visual task recording could reproduce those observed during rest, eliminating the need for a specific resting-state recording. Using MEG from 166 participants, leakage-corrected amplitude envelope correlations were calculated, yielding frequency-specific static connectivity maps for each person. This was done for both a resting-state recording and a visual-gamma recording i.e. in the latter the presence of the task was ignored during analysis. Connectivity maps, and sub-networks generated by hierarchical clustering, were compared across the two datasets using inter-session correlation. We also found a significant correlation between resting-state MEG connectivity and age and explored whether this was reproduced in the maps derived from the visual gamma data. Preliminary findings reveal moderate inter-session correlations (mean r = 0.56) in the beta-band (13-30 Hz) between FC matrices. Hierarchical clustering identified 26 stable sub-networks with significant cross-session correlations (r = 0.50–0.71, p < .001). We also observed highly reproducible age-related connectivity patterns in the alpha band (8-13 Hz) across both rest and task data (r = 0.84, p < .001). This work challenges the convention that resting-state MEG is uniquely suited for capturing connectivity and shows that task MEG data can reveal the same core features of intrinsic brain architecture, potentially substituting for rest in contexts where time, cost, or participant compliance is limited. This offers an efficient, pragmatic and powerful approach, streamlining MEG protocols and enhancing accessibility, especially in clinical or developmental populations. Future work will extend this analysis to study state-dynamics, activity, peak frequency, other tasks and clinical populations.
Methods for MEG
10:45 – 11:00
Short talk
Short talk
Multi-Scale Brain Dynamics in M/EEG with Time-Delay Embedded Hidden Markov Models
Fabrice Guibert
Ecole Polytechnique Fédérale de Lausanne (EPFL); University of Geneva (UNIGE)
Fabrice Guibert
Ecole Polytechnique Fédérale de Lausanne (EPFL); University of Geneva (UNIGE)
More details Less details
Co-authors: Fabrice Guibert, Jeroen Van Schependom, Chiara Rossi, Dimitri Van de Ville, Daphné Bavelier
Abstract:
M/EEG studies have successfully described brain activity through the succession of different states. In the context of the time-delay embedding (TDE)-hidden Markov models (HMM) methodology, these spatiotemporal states have both spatial and oscillatory properties. TDE-HMM states reflect changes in spatio-temporal covariance structures. Yet, despite the well-accepted view that the brain functions at multiple temporal scales, current analyses have primarily focused on the trial level. Objective. We aim to investigate how TDE-HMM-state time courses behave across different temporal scales. Methods. We use cryogenic MEG data collected at two sites (Brussels, N=38; Nottingham, N=8-replication data set). Each task is structured in blocks of either 0-back, 1-back, or 2-back,  interleaved in pseudo-random order, and separated by periods of instruction, as well as rest – thus providing a rich higher-order block structure. Following standard MEG preprocessing steps, we train a TDE-HMM model and extract state probability time courses. To investigate whether we can extract dynamics at multiple temporal scales, we first ask if probability time courses can be used to retrieve task-related conditions at the block level, such as being on-task versus off-task, N-back blocks of differing difficulty, and ordering effects of blocks. We then verify if probability time courses can also be used to contrast task-related conditions at the trial level i.e. hits against correct rejects. Importantly, these evaluations are conducted multiple window sizes in the TDE step of the HMM, and evaluate discriminability. Stability is assessed using multiple restarts. Results. We find that states exhibit a rich structure at the trial level, consistent with previous studies. We also demonstrate that states capture block-level structure, such that state activations distinguish between being on- and off-task, being in different N-back difficulty blocks, as well as ordering effects on N-back blocks. Thus, state time courses show striking temporal structure, yet also capture finer patterns at the trial level. Our results are stable across model restarts. Finally, we also demonstrate the influence of window size, as well as a phase transition in state power spectrum for window sizes longer than 80 ms. Conclusion. This study suggests that brain state dynamics should be considered not only at the trial level in M/EEG data, but also at a coarser level to unveil a greater range of temporal dynamics.
Abstract:
M/EEG studies have successfully described brain activity through the succession of different states. In the context of the time-delay embedding (TDE)-hidden Markov models (HMM) methodology, these spatiotemporal states have both spatial and oscillatory properties. TDE-HMM states reflect changes in spatio-temporal covariance structures. Yet, despite the well-accepted view that the brain functions at multiple temporal scales, current analyses have primarily focused on the trial level. Objective. We aim to investigate how TDE-HMM-state time courses behave across different temporal scales. Methods. We use cryogenic MEG data collected at two sites (Brussels, N=38; Nottingham, N=8-replication data set). Each task is structured in blocks of either 0-back, 1-back, or 2-back,  interleaved in pseudo-random order, and separated by periods of instruction, as well as rest – thus providing a rich higher-order block structure. Following standard MEG preprocessing steps, we train a TDE-HMM model and extract state probability time courses. To investigate whether we can extract dynamics at multiple temporal scales, we first ask if probability time courses can be used to retrieve task-related conditions at the block level, such as being on-task versus off-task, N-back blocks of differing difficulty, and ordering effects of blocks. We then verify if probability time courses can also be used to contrast task-related conditions at the trial level i.e. hits against correct rejects. Importantly, these evaluations are conducted multiple window sizes in the TDE step of the HMM, and evaluate discriminability. Stability is assessed using multiple restarts. Results. We find that states exhibit a rich structure at the trial level, consistent with previous studies. We also demonstrate that states capture block-level structure, such that state activations distinguish between being on- and off-task, being in different N-back difficulty blocks, as well as ordering effects on N-back blocks. Thus, state time courses show striking temporal structure, yet also capture finer patterns at the trial level. Our results are stable across model restarts. Finally, we also demonstrate the influence of window size, as well as a phase transition in state power spectrum for window sizes longer than 80 ms. Conclusion. This study suggests that brain state dynamics should be considered not only at the trial level in M/EEG data, but also at a coarser level to unveil a greater range of temporal dynamics.
11:00 – 11:30
Tea break
Mary Ward Hall
Mary Ward Hall
Deep Learning
11:30 – 11:45
Short talk
Short talk
Ephys-GPT: A foundation model for electrophysiological data
Rukuang Huang
University of Oxford
Rukuang Huang
University of Oxford
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Co-authors: Sungjun Cho, Mark Woolrich
Abstract:
Foundation models have demonstrated remarkable success across different domains by leveraging large-scale, unlabelled datasets and self-supervised learning to extract rich, transferable representations. For electrophysiological data, however, existing models are predominantly trained on transformed versions of the data in the time-frequency domain (e.g. with Fourier or wavelet transforms), which may compromise the temporal and frequency resolution and relies on pre-defined hyper-parameters of the transformations. We introduce Ephys-GPT, a foundation model pre-trained on large amount of raw resting-state magnetoencephalography (MEG) recordings. Inspired by the autoregressive objectives of the GPT models, Ephys-GPT is trained on tokenised raw data with a bespoke tokeniser to predict future tokens. We show that Ephys-GPT generates realistic neural recordings that preserves key statistical and physiological properties, including power spectral density, spatial patterns of frequency bands, between-subject variability, and importantly, oscillatory bursting dynamics (e.g. beta bursts in the motor cortex). Furthermore, the model can be efficiently fine-tuned on limited task-evoked data. Generated data from the fine-tuned model shows time-locked task responses to surrogate task event sequences. This work demonstrates the feasibility and potential of large-scale, self-supervised foundation models on raw electrophysiological signals, paving the way for powerful general-purpose, multi-modal tools in neural decoding and computational neuroscience.
Abstract:
Foundation models have demonstrated remarkable success across different domains by leveraging large-scale, unlabelled datasets and self-supervised learning to extract rich, transferable representations. For electrophysiological data, however, existing models are predominantly trained on transformed versions of the data in the time-frequency domain (e.g. with Fourier or wavelet transforms), which may compromise the temporal and frequency resolution and relies on pre-defined hyper-parameters of the transformations. We introduce Ephys-GPT, a foundation model pre-trained on large amount of raw resting-state magnetoencephalography (MEG) recordings. Inspired by the autoregressive objectives of the GPT models, Ephys-GPT is trained on tokenised raw data with a bespoke tokeniser to predict future tokens. We show that Ephys-GPT generates realistic neural recordings that preserves key statistical and physiological properties, including power spectral density, spatial patterns of frequency bands, between-subject variability, and importantly, oscillatory bursting dynamics (e.g. beta bursts in the motor cortex). Furthermore, the model can be efficiently fine-tuned on limited task-evoked data. Generated data from the fine-tuned model shows time-locked task responses to surrogate task event sequences. This work demonstrates the feasibility and potential of large-scale, self-supervised foundation models on raw electrophysiological signals, paving the way for powerful general-purpose, multi-modal tools in neural decoding and computational neuroscience.
Deep Learning
11:45 – 12:00
Short talk
Short talk
Learnable Sample-Level Tokenisation for MEG Foundation Models
Sungjun Cho
University of Oxford
Sungjun Cho
University of Oxford
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Co-authors: Rukuang Huang, Oiwi Parker Jones, Mark W Woolrich
Abstract:
Recent advancements in large language models have catalysed the development of transformer-based foundation models for MEG and other neuroimaging modalities, aiming to extract generalisable patterns from large datasets that can be flexibly adapted to various modalities and clinical disorders with minimal retraining. This endeavour in turn necessitated efficient tokenisation strategies that can compactly summarise neural data into transformer-compatible representations. Until now, existing tokenisers primarily adapted techniques designed for general, non-biological time-series data, such as patching, time-frequency transformations, or vector quantisation. However, these often sacrifice temporal resolution, limiting interpretability and precise temporal alignment essential for MEG data analyses. While some tokenisers do preserve temporal fidelity (e.g., mu-transform tokenisation), they are not data-adaptive and may poorly capture temporal dependencies and latent structures in MEG signals. To address these limitations, we propose a new learnable tokeniser that models tokens using convolution kernels. These kernels are simultaneously learnt and fit to the MEG data using a recurrent neural network (RNN). Crucially, this maintains full temporal resolution (i.e., a sample-level tokenisation) and enables a tokeniser to model causal structure in sequential data. We evaluated our method through a signal reconstruction task, benchmarking its performance against traditional non-learnable approaches. Our tokeniser achieved a strong reconstruction accuracy, explaining over 97% of the variance in both simulated and real resting-state MEG data, while also accounting for subject-level variability. Furthermore, it required significantly fewer tokens (90-120) than the conventional mu-transform method (256 tokens) and generalised robustly across datasets and MEG scanner types. When a transformer model was trained on the derived tokens, it achieved higher token prediction accuracy with our tokeniser, explaining more variance in the original signals. In conclusion, we present the first data-adaptive, sample-level tokenisation framework based on convolution kernels and RNN-based inference, capable of capturing fine-grained temporal dynamics suitable for transformer-based MEG foundation models. This method offers enhanced temporal resolution and prediction accuracy over existing approaches and holds promise for facilitating more reliable foundation models in neuroimaging.
Abstract:
Recent advancements in large language models have catalysed the development of transformer-based foundation models for MEG and other neuroimaging modalities, aiming to extract generalisable patterns from large datasets that can be flexibly adapted to various modalities and clinical disorders with minimal retraining. This endeavour in turn necessitated efficient tokenisation strategies that can compactly summarise neural data into transformer-compatible representations. Until now, existing tokenisers primarily adapted techniques designed for general, non-biological time-series data, such as patching, time-frequency transformations, or vector quantisation. However, these often sacrifice temporal resolution, limiting interpretability and precise temporal alignment essential for MEG data analyses. While some tokenisers do preserve temporal fidelity (e.g., mu-transform tokenisation), they are not data-adaptive and may poorly capture temporal dependencies and latent structures in MEG signals. To address these limitations, we propose a new learnable tokeniser that models tokens using convolution kernels. These kernels are simultaneously learnt and fit to the MEG data using a recurrent neural network (RNN). Crucially, this maintains full temporal resolution (i.e., a sample-level tokenisation) and enables a tokeniser to model causal structure in sequential data. We evaluated our method through a signal reconstruction task, benchmarking its performance against traditional non-learnable approaches. Our tokeniser achieved a strong reconstruction accuracy, explaining over 97% of the variance in both simulated and real resting-state MEG data, while also accounting for subject-level variability. Furthermore, it required significantly fewer tokens (90-120) than the conventional mu-transform method (256 tokens) and generalised robustly across datasets and MEG scanner types. When a transformer model was trained on the derived tokens, it achieved higher token prediction accuracy with our tokeniser, explaining more variance in the original signals. In conclusion, we present the first data-adaptive, sample-level tokenisation framework based on convolution kernels and RNN-based inference, capable of capturing fine-grained temporal dynamics suitable for transformer-based MEG foundation models. This method offers enhanced temporal resolution and prediction accuracy over existing approaches and holds promise for facilitating more reliable foundation models in neuroimaging.
12:00 – 12:30
Flash talks
Flash talks
Session 2 flash talks
Mary Ward Hall
Mary Ward Hall
12:30 – 14:00
Lunch and poster session 2
Ground Floor
Ground Floor
Clinical Neuroscience
14:00 – 14:30
Long talk
Long talk
MEG in Psychosis: individual differences in neural oscillations underlying language disorganization and impoverishment
Hsi (Tiana) Wei
McGill University; Douglas Mental Health Institute
Hsi (Tiana) Wei
McGill University; Douglas Mental Health Institute
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Co-authors: Hsi (Tiana) Wei, Dominic Boutet, Rukun Dou, Jessica Ahrens, Nadia Zeramdini, Alban Voppel, Fernando Miguel Gonzales Aste, Sylvain Baillet, Lena Palaniyappan
Abstract:
Schizophrenia is characterized by incoherent speech and reduced linguistic output, associated with neural dysconnectivity and aberrant oscillatory activity. However, the relationship between these neuronal changes and communication deficits remains unclear. This project explores the hypothesis that neuronal dysfunction underlies language disorganization and impoverishment by investigating associations between neuronal oscillations during visuo-audio integration and language features derived via automated processing pipelines in individuals with and without psychosis. Twenty-five patients with schizophrenia and 25 healthy controls completed symptom and speech assessments, Magnetoencephalography (MEG) during an audiovisual task and resting state and structural MRI. MEG recordings were obtained during an audiovisual simultaneity judgment task and open-eye resting. MEG data were source-localized to each participant’s normalized structural MRI, preprocessed, and epoched to motor responses and sensory stimuli to assess event-related power modulations. Speech data collected during interviews were analyzed for acoustic/linguistic features using Python. Preliminary analyses of 16 controls (Age M=31.81, SD=9.59) and 13 schizophrenia (SZ) patients (Age M=34.46, SD=9.38) revealed attenuated post-movement beta rebound (PMBR) in patients, bilaterally in frontal regions. Reduced PMBR likely suggests diminished interhemispheric beta-mediated functional inhibition. Notably, weaker PMBR correlated with hallucinatory behavior (r(27)=-.38, p=0.04) and blunted affect (r(27)=-.38, p=0.04) on the PANSS. Speech analysis showed that apathetic social withdrawal was linked to fewer syllables (r(27)=-.41, p=0.03) and unnatural mannerisms and postures on PANSS related with reduced syllables (r(27)=-.51, p<0.01), phonation time (r(27)=-.48, p<0.01), and pauses (r(27)=-.38, p=0.04). Stronger PMBR in the frontal region correlated with greater syllable production (r(27)=.37, p<0.05). These findings highlight associations between beta-band power, clinical symptoms, and speech performance, with PMBR strongest in controls, followed by more verbal patients, and weakest in less verbal patients. Upcoming analyses will include personalized spectral power characteristics, bilateral frontotemporal oscillatory connectivity. With a more comprehensive sample size and analysis, this project aims to elucidate individual differences linking neuronal oscillations to language symptoms in psychosis.
Abstract:
Schizophrenia is characterized by incoherent speech and reduced linguistic output, associated with neural dysconnectivity and aberrant oscillatory activity. However, the relationship between these neuronal changes and communication deficits remains unclear. This project explores the hypothesis that neuronal dysfunction underlies language disorganization and impoverishment by investigating associations between neuronal oscillations during visuo-audio integration and language features derived via automated processing pipelines in individuals with and without psychosis. Twenty-five patients with schizophrenia and 25 healthy controls completed symptom and speech assessments, Magnetoencephalography (MEG) during an audiovisual task and resting state and structural MRI. MEG recordings were obtained during an audiovisual simultaneity judgment task and open-eye resting. MEG data were source-localized to each participant’s normalized structural MRI, preprocessed, and epoched to motor responses and sensory stimuli to assess event-related power modulations. Speech data collected during interviews were analyzed for acoustic/linguistic features using Python. Preliminary analyses of 16 controls (Age M=31.81, SD=9.59) and 13 schizophrenia (SZ) patients (Age M=34.46, SD=9.38) revealed attenuated post-movement beta rebound (PMBR) in patients, bilaterally in frontal regions. Reduced PMBR likely suggests diminished interhemispheric beta-mediated functional inhibition. Notably, weaker PMBR correlated with hallucinatory behavior (r(27)=-.38, p=0.04) and blunted affect (r(27)=-.38, p=0.04) on the PANSS. Speech analysis showed that apathetic social withdrawal was linked to fewer syllables (r(27)=-.41, p=0.03) and unnatural mannerisms and postures on PANSS related with reduced syllables (r(27)=-.51, p<0.01), phonation time (r(27)=-.48, p<0.01), and pauses (r(27)=-.38, p=0.04). Stronger PMBR in the frontal region correlated with greater syllable production (r(27)=.37, p<0.05). These findings highlight associations between beta-band power, clinical symptoms, and speech performance, with PMBR strongest in controls, followed by more verbal patients, and weakest in less verbal patients. Upcoming analyses will include personalized spectral power characteristics, bilateral frontotemporal oscillatory connectivity. With a more comprehensive sample size and analysis, this project aims to elucidate individual differences linking neuronal oscillations to language symptoms in psychosis.
Clinical Neuroscience
14:30 – 14:45
Short talk
Short talk
Weakened prefrontal activation dynamics associated with slowed information processing speed in multiple sclerosis
Olivier Burta
Vrije Universiteit Brussel
Olivier Burta
Vrije Universiteit Brussel
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Co-authors: Fahimeh Akbarian, Chiara Rossi, Diego Vidaurre, Marie Bie D’hooghe, Miguel D’Haeseleer, Guy Nagels, Jeroen Van Schependom
Abstract:
Information processing speed (IPS) is a core cognitive deficit in people with multiple sclerosis (PwMS). Previous efforts have associated IPS performance to frontal regions, but were constrained by limited temporal resolution. In this work, we employed a data-driven method, the time delay embedded-hidden Markov model (TDE-HMM), to identify task-specific states that are spectrally defined with distinct temporal and spatial profiles. We used magnetoencephalographic (MEG) data recorded while healthy controls and PwMS performed a cognitive task designed to capture IPS, the Symbol Digit Modalities Test (SDMT). The TDE-HMM identified five task-relevant states, supporting a tri-factor contribution to IPS: sensory speed (occipital visual detection and processing), cognitive speed (prefrontal executive and frontoparietal attention shift), and motor speed (sensorimotor). We observed reduced prefrontal and increased frontoparietal activation in PwMS, which significantly correlated with offline SDMT performance. This work can drive future research for MS treatments targeting IPS improvements.
Abstract:
Information processing speed (IPS) is a core cognitive deficit in people with multiple sclerosis (PwMS). Previous efforts have associated IPS performance to frontal regions, but were constrained by limited temporal resolution. In this work, we employed a data-driven method, the time delay embedded-hidden Markov model (TDE-HMM), to identify task-specific states that are spectrally defined with distinct temporal and spatial profiles. We used magnetoencephalographic (MEG) data recorded while healthy controls and PwMS performed a cognitive task designed to capture IPS, the Symbol Digit Modalities Test (SDMT). The TDE-HMM identified five task-relevant states, supporting a tri-factor contribution to IPS: sensory speed (occipital visual detection and processing), cognitive speed (prefrontal executive and frontoparietal attention shift), and motor speed (sensorimotor). We observed reduced prefrontal and increased frontoparietal activation in PwMS, which significantly correlated with offline SDMT performance. This work can drive future research for MS treatments targeting IPS improvements.
Clinical Neuroscience
14:45 – 15:00
Short talk
Short talk
Varying patterns of association between cortical large-scale networks and subthalamic nucleus activity in Parkinson’s Disease
Oliver Kohl
Heinrich-Heine-University Düsseldorf
Oliver Kohl
Heinrich-Heine-University Düsseldorf
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Co-authors: Chetan Gohil, Matthias Sure, Alfons Schnitzler, Esther Florin
Abstract:
Parkinson’s Disease (PD) is characterised by the progressive degeneration of dopaminergic neurons and the accumulation of Lewy bodies in the substantia nigra pars compacta. This pathology disrupts dopaminergic regulation of the basal ganglia, leading to motor impairments. While basal ganglia activity is known to synchronise with specific cortical regions, the broader dynamics of cortical network involvement remain unclear. To investigate this, we analysed simultaneous magnetoencephalography (MEG) and subthalamic nucleus (STN) local field potential (LFP) recordings from 25 individuals with PD, both on and off dopaminergic medication. We identified dynamic large-scale cortical networks with a Time-Delay Embedded Hidden Markov Model that showed distinct patterns of STN-cortical coherence. Notably, increased synchrony between the STN and supplementary motor area (SMA) occurred during activation of a sensorimotor network and a network characterised by widespread cortical power increases. The sensorimotor network was associated with elevated STN 9.5 to 23-Hz power and beta bursts, while the widespread activation network was linked to increased STN power in the 5 to 16.5-Hz range. These findings were replicated in a second dataset of 17 additional participants. Interestingly, dopaminergic medication most strongly reduced STN beta power during activation of cortical networks that did not show increased STN-motor cortical coherence. Overall, our results indicate that large-scale cortical networks exhibit STN-cortical communication in distinct ways. The sensorimotor and widespread activation networks, in particular, may serve as spatiotemporal windows into subcortical STN processing. These cortical network signatures in non-invasive recordings may offer a novel avenue for accessing subcortical information relevant to PD, potentially informing diagnosis and treatment strategies.
Abstract:
Parkinson’s Disease (PD) is characterised by the progressive degeneration of dopaminergic neurons and the accumulation of Lewy bodies in the substantia nigra pars compacta. This pathology disrupts dopaminergic regulation of the basal ganglia, leading to motor impairments. While basal ganglia activity is known to synchronise with specific cortical regions, the broader dynamics of cortical network involvement remain unclear. To investigate this, we analysed simultaneous magnetoencephalography (MEG) and subthalamic nucleus (STN) local field potential (LFP) recordings from 25 individuals with PD, both on and off dopaminergic medication. We identified dynamic large-scale cortical networks with a Time-Delay Embedded Hidden Markov Model that showed distinct patterns of STN-cortical coherence. Notably, increased synchrony between the STN and supplementary motor area (SMA) occurred during activation of a sensorimotor network and a network characterised by widespread cortical power increases. The sensorimotor network was associated with elevated STN 9.5 to 23-Hz power and beta bursts, while the widespread activation network was linked to increased STN power in the 5 to 16.5-Hz range. These findings were replicated in a second dataset of 17 additional participants. Interestingly, dopaminergic medication most strongly reduced STN beta power during activation of cortical networks that did not show increased STN-motor cortical coherence. Overall, our results indicate that large-scale cortical networks exhibit STN-cortical communication in distinct ways. The sensorimotor and widespread activation networks, in particular, may serve as spatiotemporal windows into subcortical STN processing. These cortical network signatures in non-invasive recordings may offer a novel avenue for accessing subcortical information relevant to PD, potentially informing diagnosis and treatment strategies.
Clinical Neuroscience
15:00 – 15:15
Short talk
Short talk
Impaired mPFC–hippocampal theta phase coupling during memory retrieval in Schizophrenia
Ingrid Martin
Kings College London
Ingrid Martin
Kings College London
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Co-authors: Daniel Bush, Rick Adams, Neil Burgess
Abstract:
Theta-band (1-7Hz) oscillations and long-range phase coupling within the hippocampal–medial prefrontal cortex (HPC–mPFC) network are critical for memory function and have been extensively characterized in animal models. However, their role in human cognition and psychiatric disorders such as schizophrenia remains poorly understood. This study used magnetoencephalography (MEG) to investigate theta oscillatory dynamics during an associative inference task in patients with schizophrenia and matched healthy controls. Patients exhibited marked impairments in recognition memory, including elevated false alarm rates, and showed deficits in both direct and inferential memory retrieval. While both groups demonstrated increased mPFC theta power and HPC–mPFC theta coupling during encoding, only healthy controls maintained this coupling at retrieval. In contrast, patients showed a breakdown in theta phase coupling during memory retrieval, pointing to a functional disconnection within the HPC–mPFC network. These findings extend prior rodent models of hippocampal–prefrontal interactions to the human domain and provide novel evidence that schizophrenia is associated with task-specific disruptions in theta synchrony. This suggests a potential neural mechanism underlying relational memory impairments in psychosis, with implications for targeting HPC–PFC network dysfunction in therapeutic interventions.
Abstract:
Theta-band (1-7Hz) oscillations and long-range phase coupling within the hippocampal–medial prefrontal cortex (HPC–mPFC) network are critical for memory function and have been extensively characterized in animal models. However, their role in human cognition and psychiatric disorders such as schizophrenia remains poorly understood. This study used magnetoencephalography (MEG) to investigate theta oscillatory dynamics during an associative inference task in patients with schizophrenia and matched healthy controls. Patients exhibited marked impairments in recognition memory, including elevated false alarm rates, and showed deficits in both direct and inferential memory retrieval. While both groups demonstrated increased mPFC theta power and HPC–mPFC theta coupling during encoding, only healthy controls maintained this coupling at retrieval. In contrast, patients showed a breakdown in theta phase coupling during memory retrieval, pointing to a functional disconnection within the HPC–mPFC network. These findings extend prior rodent models of hippocampal–prefrontal interactions to the human domain and provide novel evidence that schizophrenia is associated with task-specific disruptions in theta synchrony. This suggests a potential neural mechanism underlying relational memory impairments in psychosis, with implications for targeting HPC–PFC network dysfunction in therapeutic interventions.
Clinical Neuroscience
15:15 – 15:30
Short talk
Short talk
High-density full-head on-scalp MEG for Epilepsy
Svenja Knappe
FieldLine Medical; University of Colorado Boulder
Svenja Knappe
FieldLine Medical; University of Colorado Boulder
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Co-authors: Svenja Knappe, Isabelle Buard, K. Jeramy Hughes, Orang Alem, Tyler Maydew, Eugene Kronberg, Peter Teale, Teresa Cheung
Abstract:
Optically-pumped magnetometers (OPMs) have been identified as a possible candidate for use in evaluations of patients with epilepsy. We present first results of an ongoing cross-validation study performed in 20 adult patients with drug-resistant focal epilepsy to date. In addition, sensory-evoked activity was recorded and localized in the patients and a set of healthy controls. The goal of the study is to compare the data quality between OPM-based MEG and conventional cryogenic MEG, using simultaneous EEG and MEG recordings. Methods: To assess the OPM data quality, subjects underwent simultaneously EEG and MEG resting-state recordings on a cryogenic MEG system and an on-scalp MEG system for 30 min each. Co-registration with the subject’s anatomy was performed by digitizing the positions of five head-position indicator (HPI) coils with respect to three fiducials and localizing them with the MEG system. The resting data were filtered with a bandpass filter from 3 – 70 Hz or 20 – 70 and a notch filter at 60 Hz. Bad segments containing muscle activity were marked, and a kurtosis was calculated. Thresholds in the volumetric images were used to identify the peak locations of high kurtosis, where virtual channels were computed. Peaks were marked for comparison with the EEG signals and for dipole fits. For the sensory mapping study, auditory, visual, somatosensory, and motor areas were localized both by performing dipole fits and event-related beamformer analysis. Results: Clear interictal spikes were recorded at the same time points and exhibit similar morphology in several patients between the EEG and OPM recordings, consistent with the EEG and cryogenic MEG results. There was also good agreement between the OPM and cryogenic MEG resting data. The results of the sensory study agreed closely between both the OPM and cryogenic MEG recordings and were consistent with results found in literature. Conclusions: Good agreement was found between the on-scalp MEG and the EEG data. The kurtosis beamformer presents a convenient method for localization of interictal activity and agreed well with the dipole fits. The sensory study showed that the OPM HEDscan system localized sensory-evoked fields reliably and yielded similar data quality to cryogenic MEG systems. The results will have to be validated systematically in a larger number of subjects.
Abstract:
Optically-pumped magnetometers (OPMs) have been identified as a possible candidate for use in evaluations of patients with epilepsy. We present first results of an ongoing cross-validation study performed in 20 adult patients with drug-resistant focal epilepsy to date. In addition, sensory-evoked activity was recorded and localized in the patients and a set of healthy controls. The goal of the study is to compare the data quality between OPM-based MEG and conventional cryogenic MEG, using simultaneous EEG and MEG recordings. Methods: To assess the OPM data quality, subjects underwent simultaneously EEG and MEG resting-state recordings on a cryogenic MEG system and an on-scalp MEG system for 30 min each. Co-registration with the subject’s anatomy was performed by digitizing the positions of five head-position indicator (HPI) coils with respect to three fiducials and localizing them with the MEG system. The resting data were filtered with a bandpass filter from 3 – 70 Hz or 20 – 70 and a notch filter at 60 Hz. Bad segments containing muscle activity were marked, and a kurtosis was calculated. Thresholds in the volumetric images were used to identify the peak locations of high kurtosis, where virtual channels were computed. Peaks were marked for comparison with the EEG signals and for dipole fits. For the sensory mapping study, auditory, visual, somatosensory, and motor areas were localized both by performing dipole fits and event-related beamformer analysis. Results: Clear interictal spikes were recorded at the same time points and exhibit similar morphology in several patients between the EEG and OPM recordings, consistent with the EEG and cryogenic MEG results. There was also good agreement between the OPM and cryogenic MEG resting data. The results of the sensory study agreed closely between both the OPM and cryogenic MEG recordings and were consistent with results found in literature. Conclusions: Good agreement was found between the on-scalp MEG and the EEG data. The kurtosis beamformer presents a convenient method for localization of interictal activity and agreed well with the dipole fits. The sensory study showed that the OPM HEDscan system localized sensory-evoked fields reliably and yielded similar data quality to cryogenic MEG systems. The results will have to be validated systematically in a larger number of subjects.
15:30 – 16:00
Closing and award ceremony
Yulia Bezsudnova, Gareth Barnes
University College London
Yulia Bezsudnova, Gareth Barnes
University College London
16:00 – 17:00
Tea break
Ground Floor
Ground Floor
** “Naturalistic neuroscience” day – 16th July:
As brain research increasingly shifts toward studying neural activity in more naturalistic settings, new technologies are being developed — and existing ones adapted — to meet this challenge. The first day of MEGUKI will highlight cutting-edge experiments leveraging neuronal signals (EEG, OP-MEG, fNIRS) to investigate brain and spinal function in real-world-like contexts. Our keynote speakers, Professor Dominik Bach and Dr Jamie Ward, will share their insights and latest research in this exciting area. We hope this day will inspire and connect researchers who are pushing the boundaries of naturalistic neuroscience.
