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Discovery of key whole-brain transitions and dynamics during human wakefulness and non-REM sleep

The modern understanding of sleep is based on the classification of sleep into stages defined by their electroencephalography (EEG) signatures, but the underlying brain dynamics remain unclear. Here we aimed to move significantly beyond the current state-of-the-art description of sleep, and in parti...

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Autores principales: Stevner, A. B. A., Vidaurre, D., Cabral, J., Rapuano, K., Nielsen, S. F. V., Tagliazucchi, E., Laufs, H., Vuust, P., Deco, G., Woolrich, M. W., Van Someren, E., Kringelbach, M. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399232/
https://www.ncbi.nlm.nih.gov/pubmed/30833560
http://dx.doi.org/10.1038/s41467-019-08934-3
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author Stevner, A. B. A.
Vidaurre, D.
Cabral, J.
Rapuano, K.
Nielsen, S. F. V.
Tagliazucchi, E.
Laufs, H.
Vuust, P.
Deco, G.
Woolrich, M. W.
Van Someren, E.
Kringelbach, M. L.
author_facet Stevner, A. B. A.
Vidaurre, D.
Cabral, J.
Rapuano, K.
Nielsen, S. F. V.
Tagliazucchi, E.
Laufs, H.
Vuust, P.
Deco, G.
Woolrich, M. W.
Van Someren, E.
Kringelbach, M. L.
author_sort Stevner, A. B. A.
collection PubMed
description The modern understanding of sleep is based on the classification of sleep into stages defined by their electroencephalography (EEG) signatures, but the underlying brain dynamics remain unclear. Here we aimed to move significantly beyond the current state-of-the-art description of sleep, and in particular to characterise the spatiotemporal complexity of whole-brain networks and state transitions during sleep. In order to obtain the most unbiased estimate of how whole-brain network states evolve through the human sleep cycle, we used a Markovian data-driven analysis of continuous neuroimaging data from 57 healthy participants falling asleep during simultaneous functional magnetic resonance imaging (fMRI) and EEG. This Hidden Markov Model (HMM) facilitated discovery of the dynamic choreography between different whole-brain networks across the wake-non-REM sleep cycle. Notably, our results reveal key trajectories to switch within and between EEG-based sleep stages, while highlighting the heterogeneities of stage N1 sleep and wakefulness before and after sleep.
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spelling pubmed-63992322019-03-06 Discovery of key whole-brain transitions and dynamics during human wakefulness and non-REM sleep Stevner, A. B. A. Vidaurre, D. Cabral, J. Rapuano, K. Nielsen, S. F. V. Tagliazucchi, E. Laufs, H. Vuust, P. Deco, G. Woolrich, M. W. Van Someren, E. Kringelbach, M. L. Nat Commun Article The modern understanding of sleep is based on the classification of sleep into stages defined by their electroencephalography (EEG) signatures, but the underlying brain dynamics remain unclear. Here we aimed to move significantly beyond the current state-of-the-art description of sleep, and in particular to characterise the spatiotemporal complexity of whole-brain networks and state transitions during sleep. In order to obtain the most unbiased estimate of how whole-brain network states evolve through the human sleep cycle, we used a Markovian data-driven analysis of continuous neuroimaging data from 57 healthy participants falling asleep during simultaneous functional magnetic resonance imaging (fMRI) and EEG. This Hidden Markov Model (HMM) facilitated discovery of the dynamic choreography between different whole-brain networks across the wake-non-REM sleep cycle. Notably, our results reveal key trajectories to switch within and between EEG-based sleep stages, while highlighting the heterogeneities of stage N1 sleep and wakefulness before and after sleep. Nature Publishing Group UK 2019-03-04 /pmc/articles/PMC6399232/ /pubmed/30833560 http://dx.doi.org/10.1038/s41467-019-08934-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Stevner, A. B. A.
Vidaurre, D.
Cabral, J.
Rapuano, K.
Nielsen, S. F. V.
Tagliazucchi, E.
Laufs, H.
Vuust, P.
Deco, G.
Woolrich, M. W.
Van Someren, E.
Kringelbach, M. L.
Discovery of key whole-brain transitions and dynamics during human wakefulness and non-REM sleep
title Discovery of key whole-brain transitions and dynamics during human wakefulness and non-REM sleep
title_full Discovery of key whole-brain transitions and dynamics during human wakefulness and non-REM sleep
title_fullStr Discovery of key whole-brain transitions and dynamics during human wakefulness and non-REM sleep
title_full_unstemmed Discovery of key whole-brain transitions and dynamics during human wakefulness and non-REM sleep
title_short Discovery of key whole-brain transitions and dynamics during human wakefulness and non-REM sleep
title_sort discovery of key whole-brain transitions and dynamics during human wakefulness and non-rem sleep
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399232/
https://www.ncbi.nlm.nih.gov/pubmed/30833560
http://dx.doi.org/10.1038/s41467-019-08934-3
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