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Non-invasive detection of high gamma band activity during motor imagery

High gamma oscillations (70–150 Hz; HG) are rapidly evolving, spatially localized neurophysiological signals that are believed to be the best representative signature of engaged neural populations. The HG band has been best characterized from invasive electrophysiological approaches such as electroc...

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Autores principales: Smith, Melissa M., Weaver, Kurt E., Grabowski, Thomas J., Rao, Rajesh P. N., Darvas, Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199322/
https://www.ncbi.nlm.nih.gov/pubmed/25360100
http://dx.doi.org/10.3389/fnhum.2014.00817
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author Smith, Melissa M.
Weaver, Kurt E.
Grabowski, Thomas J.
Rao, Rajesh P. N.
Darvas, Felix
author_facet Smith, Melissa M.
Weaver, Kurt E.
Grabowski, Thomas J.
Rao, Rajesh P. N.
Darvas, Felix
author_sort Smith, Melissa M.
collection PubMed
description High gamma oscillations (70–150 Hz; HG) are rapidly evolving, spatially localized neurophysiological signals that are believed to be the best representative signature of engaged neural populations. The HG band has been best characterized from invasive electrophysiological approaches such as electrocorticography because of the increased signal-to-noise ratio that results when by-passing the scalp and skull. Despite the recent observation that HG activity can be detected non-invasively by electroencephalography (EEG), it is unclear to what extent EEG can accurately resolve the spatial distribution of HG signals during active task engagement. We have overcome some of the limitations inherent to acquiring HG signals across the scalp by utilizing individual head anatomy in combination with an inverse modeling method. We applied a linearly constrained minimum variance (LCMV) beamformer method on EEG data during a motor imagery paradigm to extract a time-frequency spectrogram at every voxel location on the cortex. To confirm spatially distributed patterns of HG responses, we contrasted overlapping maps of the EEG HG signal with blood oxygen level dependence (BOLD) functional magnetic resonance imaging (fMRI) data acquired from the same set of neurologically normal subjects during a separate session. We show that scalp-based HG band activity detected by EEG during motor imagery spatially co-localizes with BOLD fMRI data. Taken together, these results suggest that EEG can accurately resolve spatially specific estimates of local cortical high frequency signals, potentially opening an avenue for non-invasive measurement of HG potentials from diverse sets of neurologically impaired populations for diagnostic and therapeutic purposes.
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spelling pubmed-41993222014-10-30 Non-invasive detection of high gamma band activity during motor imagery Smith, Melissa M. Weaver, Kurt E. Grabowski, Thomas J. Rao, Rajesh P. N. Darvas, Felix Front Hum Neurosci Neuroscience High gamma oscillations (70–150 Hz; HG) are rapidly evolving, spatially localized neurophysiological signals that are believed to be the best representative signature of engaged neural populations. The HG band has been best characterized from invasive electrophysiological approaches such as electrocorticography because of the increased signal-to-noise ratio that results when by-passing the scalp and skull. Despite the recent observation that HG activity can be detected non-invasively by electroencephalography (EEG), it is unclear to what extent EEG can accurately resolve the spatial distribution of HG signals during active task engagement. We have overcome some of the limitations inherent to acquiring HG signals across the scalp by utilizing individual head anatomy in combination with an inverse modeling method. We applied a linearly constrained minimum variance (LCMV) beamformer method on EEG data during a motor imagery paradigm to extract a time-frequency spectrogram at every voxel location on the cortex. To confirm spatially distributed patterns of HG responses, we contrasted overlapping maps of the EEG HG signal with blood oxygen level dependence (BOLD) functional magnetic resonance imaging (fMRI) data acquired from the same set of neurologically normal subjects during a separate session. We show that scalp-based HG band activity detected by EEG during motor imagery spatially co-localizes with BOLD fMRI data. Taken together, these results suggest that EEG can accurately resolve spatially specific estimates of local cortical high frequency signals, potentially opening an avenue for non-invasive measurement of HG potentials from diverse sets of neurologically impaired populations for diagnostic and therapeutic purposes. Frontiers Media S.A. 2014-10-16 /pmc/articles/PMC4199322/ /pubmed/25360100 http://dx.doi.org/10.3389/fnhum.2014.00817 Text en Copyright © 2014 Smith, Weaver, Grabowski, Rao and Darvas. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Smith, Melissa M.
Weaver, Kurt E.
Grabowski, Thomas J.
Rao, Rajesh P. N.
Darvas, Felix
Non-invasive detection of high gamma band activity during motor imagery
title Non-invasive detection of high gamma band activity during motor imagery
title_full Non-invasive detection of high gamma band activity during motor imagery
title_fullStr Non-invasive detection of high gamma band activity during motor imagery
title_full_unstemmed Non-invasive detection of high gamma band activity during motor imagery
title_short Non-invasive detection of high gamma band activity during motor imagery
title_sort non-invasive detection of high gamma band activity during motor imagery
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199322/
https://www.ncbi.nlm.nih.gov/pubmed/25360100
http://dx.doi.org/10.3389/fnhum.2014.00817
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