Spatiotemporal organisation of human sensorimotor beta burst activity

Beta oscillations in human sensorimotor cortex are hallmark signatures of healthy and pathological movement. In single trials, beta oscillations include bursts of intermittent, transient periods of high-power activity. These burst events have been linked to a range of sensory and motor processes, bu...

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Main Authors: Catharina Zich, Andrew J Quinn, James J Bonaiuto, George O'Neill, Lydia C Mardell, Nick S Ward, Sven Bestmann
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2023-03-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/80160
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author Catharina Zich
Andrew J Quinn
James J Bonaiuto
George O'Neill
Lydia C Mardell
Nick S Ward
Sven Bestmann
author_facet Catharina Zich
Andrew J Quinn
James J Bonaiuto
George O'Neill
Lydia C Mardell
Nick S Ward
Sven Bestmann
author_sort Catharina Zich
collection DOAJ
description Beta oscillations in human sensorimotor cortex are hallmark signatures of healthy and pathological movement. In single trials, beta oscillations include bursts of intermittent, transient periods of high-power activity. These burst events have been linked to a range of sensory and motor processes, but their precise spatial, spectral, and temporal structure remains unclear. Specifically, a role for beta burst activity in information coding and communication suggests spatiotemporal patterns, or travelling wave activity, along specific anatomical gradients. We here show in human magnetoencephalography recordings that burst activity in sensorimotor cortex occurs in planar spatiotemporal wave-like patterns that dominate along two axes either parallel or perpendicular to the central sulcus. Moreover, we find that the two propagation directions are characterised by distinct anatomical and physiological features. Finally, our results suggest that sensorimotor beta bursts occurring before and after a movement can be distinguished by their anatomical, spectral, and spatiotemporal characteristics, indicating distinct functional roles.
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spelling doaj.art-c81b206c786946afb27a5a12c89485d82023-04-17T13:57:49ZengeLife Sciences Publications LtdeLife2050-084X2023-03-011210.7554/eLife.80160Spatiotemporal organisation of human sensorimotor beta burst activityCatharina Zich0https://orcid.org/0000-0002-0705-9297Andrew J Quinn1https://orcid.org/0000-0003-2267-9897James J Bonaiuto2George O'Neill3Lydia C Mardell4https://orcid.org/0000-0003-3180-3239Nick S Ward5Sven Bestmann6https://orcid.org/0000-0002-6867-9545Department of Clinical and Movement Neuroscience, UCL Queen Square Institute of Neurology, London, United Kingdom; Wellcome Centre for Integrative Neuroimaging, FMRIB, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom; Medical Research Council Brain Network Dynamics Unit, University of Oxford, Oxford, United KingdomOxford Centre for Human Brain Activity, Wellcome Centre for Integrative Neuroimaging, Department of Psychiatry, University of Oxford, Oxford, United Kingdom; Centre for Human Brain Health, School of Psychology, University of Birmingham, Birmingham, United KingdomInstitut des Sciences Cognitives Marc Jeannerod, CNRS UMR 5229, Bron, France; Université Claude Bernard Lyon 1, Université de Lyon, Lyon, FranceWellcome Centre for Human Neuroimaging, Department of Imaging Neuroscience, UCL Queen Square Institute of Neurology, London, United KingdomDepartment of Clinical and Movement Neuroscience, UCL Queen Square Institute of Neurology, London, United KingdomDepartment of Clinical and Movement Neuroscience, UCL Queen Square Institute of Neurology, London, United KingdomDepartment of Clinical and Movement Neuroscience, UCL Queen Square Institute of Neurology, London, United Kingdom; Wellcome Centre for Human Neuroimaging, Department of Imaging Neuroscience, UCL Queen Square Institute of Neurology, London, United KingdomBeta oscillations in human sensorimotor cortex are hallmark signatures of healthy and pathological movement. In single trials, beta oscillations include bursts of intermittent, transient periods of high-power activity. These burst events have been linked to a range of sensory and motor processes, but their precise spatial, spectral, and temporal structure remains unclear. Specifically, a role for beta burst activity in information coding and communication suggests spatiotemporal patterns, or travelling wave activity, along specific anatomical gradients. We here show in human magnetoencephalography recordings that burst activity in sensorimotor cortex occurs in planar spatiotemporal wave-like patterns that dominate along two axes either parallel or perpendicular to the central sulcus. Moreover, we find that the two propagation directions are characterised by distinct anatomical and physiological features. Finally, our results suggest that sensorimotor beta bursts occurring before and after a movement can be distinguished by their anatomical, spectral, and spatiotemporal characteristics, indicating distinct functional roles.https://elifesciences.org/articles/80160beta burstsensorimotor cortextravelling waveoscillation
spellingShingle Catharina Zich
Andrew J Quinn
James J Bonaiuto
George O'Neill
Lydia C Mardell
Nick S Ward
Sven Bestmann
Spatiotemporal organisation of human sensorimotor beta burst activity
eLife
beta burst
sensorimotor cortex
travelling wave
oscillation
title Spatiotemporal organisation of human sensorimotor beta burst activity
title_full Spatiotemporal organisation of human sensorimotor beta burst activity
title_fullStr Spatiotemporal organisation of human sensorimotor beta burst activity
title_full_unstemmed Spatiotemporal organisation of human sensorimotor beta burst activity
title_short Spatiotemporal organisation of human sensorimotor beta burst activity
title_sort spatiotemporal organisation of human sensorimotor beta burst activity
topic beta burst
sensorimotor cortex
travelling wave
oscillation
url https://elifesciences.org/articles/80160
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