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Microstates and power envelope hidden Markov modeling probe bursting brain activity at different timescales

State modeling of whole-brain electroencephalography (EEG) or magnetoencephalography (MEG) allows to investigate transient, recurring neurodynamical events. Two widely-used techniques are the microstate analysis of EEG signals and hidden Markov modeling (HMM) of MEG power envelopes. Both reportedly...

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Autores principales: Coquelet, N., De Tiège, X., Roshchupkina, L., Peigneux, P., Goldman, S., Woolrich, M., Wens, V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803543/
https://www.ncbi.nlm.nih.gov/pubmed/34954027
http://dx.doi.org/10.1016/j.neuroimage.2021.118850
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author Coquelet, N.
De Tiège, X.
Roshchupkina, L.
Peigneux, P.
Goldman, S.
Woolrich, M.
Wens, V.
author_facet Coquelet, N.
De Tiège, X.
Roshchupkina, L.
Peigneux, P.
Goldman, S.
Woolrich, M.
Wens, V.
author_sort Coquelet, N.
collection PubMed
description State modeling of whole-brain electroencephalography (EEG) or magnetoencephalography (MEG) allows to investigate transient, recurring neurodynamical events. Two widely-used techniques are the microstate analysis of EEG signals and hidden Markov modeling (HMM) of MEG power envelopes. Both reportedly lead to similar state lifetimes on the 100 ms timescale, suggesting a common neural basis. To investigate whether microstates and power envelope HMM states describe the same neural dynamics, we used simultaneous MEG/EEG recordings at rest and compared the spatial signature and temporal activation dynamics of microstates and power envelope HMM states obtained separately from EEG and MEG. Results showed that microstates and power envelope HMM states differ both spatially and temporally. Microstates reflect sharp events of neural synchronization, whereas power envelope HMM states disclose network-level activity with 100–200 ms lifetimes. Further, MEG microstates do not correspond to the canonical EEG microstates but are better interpreted as split HMM states. On the other hand, both MEG and EEG HMM states involve the (de)activation of similar functional networks. Microstate analysis and power envelope HMM thus appear sensitive to neural events occurring over different spatial and temporal scales. As such, they represent complementary approaches to explore the fast, sub-second scale bursting electrophysiological dynamics in spontaneous human brain activity.
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spelling pubmed-88035432022-02-15 Microstates and power envelope hidden Markov modeling probe bursting brain activity at different timescales Coquelet, N. De Tiège, X. Roshchupkina, L. Peigneux, P. Goldman, S. Woolrich, M. Wens, V. Neuroimage Article State modeling of whole-brain electroencephalography (EEG) or magnetoencephalography (MEG) allows to investigate transient, recurring neurodynamical events. Two widely-used techniques are the microstate analysis of EEG signals and hidden Markov modeling (HMM) of MEG power envelopes. Both reportedly lead to similar state lifetimes on the 100 ms timescale, suggesting a common neural basis. To investigate whether microstates and power envelope HMM states describe the same neural dynamics, we used simultaneous MEG/EEG recordings at rest and compared the spatial signature and temporal activation dynamics of microstates and power envelope HMM states obtained separately from EEG and MEG. Results showed that microstates and power envelope HMM states differ both spatially and temporally. Microstates reflect sharp events of neural synchronization, whereas power envelope HMM states disclose network-level activity with 100–200 ms lifetimes. Further, MEG microstates do not correspond to the canonical EEG microstates but are better interpreted as split HMM states. On the other hand, both MEG and EEG HMM states involve the (de)activation of similar functional networks. Microstate analysis and power envelope HMM thus appear sensitive to neural events occurring over different spatial and temporal scales. As such, they represent complementary approaches to explore the fast, sub-second scale bursting electrophysiological dynamics in spontaneous human brain activity. Academic Press 2022-02-15 /pmc/articles/PMC8803543/ /pubmed/34954027 http://dx.doi.org/10.1016/j.neuroimage.2021.118850 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Coquelet, N.
De Tiège, X.
Roshchupkina, L.
Peigneux, P.
Goldman, S.
Woolrich, M.
Wens, V.
Microstates and power envelope hidden Markov modeling probe bursting brain activity at different timescales
title Microstates and power envelope hidden Markov modeling probe bursting brain activity at different timescales
title_full Microstates and power envelope hidden Markov modeling probe bursting brain activity at different timescales
title_fullStr Microstates and power envelope hidden Markov modeling probe bursting brain activity at different timescales
title_full_unstemmed Microstates and power envelope hidden Markov modeling probe bursting brain activity at different timescales
title_short Microstates and power envelope hidden Markov modeling probe bursting brain activity at different timescales
title_sort microstates and power envelope hidden markov modeling probe bursting brain activity at different timescales
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803543/
https://www.ncbi.nlm.nih.gov/pubmed/34954027
http://dx.doi.org/10.1016/j.neuroimage.2021.118850
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