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Slow wave synchronization and sleep state transitions
Spontaneous synchronization over large networks is ubiquitous in nature, ranging from inanimate to biological systems. In the human brain, neuronal synchronization and de-synchronization occur during sleep, with the greatest degree of neuronal synchronization during slow wave sleep (SWS). The curren...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076647/ https://www.ncbi.nlm.nih.gov/pubmed/35523989 http://dx.doi.org/10.1038/s41598-022-11513-0 |
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author | Guo, Dan Thomas, Robert J. Liu, Yanhui Shea, Steven A. Lu, Jun Peng, Chung-Kang |
author_facet | Guo, Dan Thomas, Robert J. Liu, Yanhui Shea, Steven A. Lu, Jun Peng, Chung-Kang |
author_sort | Guo, Dan |
collection | PubMed |
description | Spontaneous synchronization over large networks is ubiquitous in nature, ranging from inanimate to biological systems. In the human brain, neuronal synchronization and de-synchronization occur during sleep, with the greatest degree of neuronal synchronization during slow wave sleep (SWS). The current sleep classification schema is based on electroencephalography and provides common criteria for clinicians and researchers to describe stages of non-rapid eye movement (NREM) sleep as well as rapid eye movement (REM) sleep. These sleep stage classifications have been based on convenient heuristic criteria, with little consideration of the accompanying normal physiological changes across those same sleep stages. To begin to resolve those inconsistencies, first focusing only on NREM sleep, we propose a simple cluster synchronization model to explain the emergence of SWS in healthy people without sleep disorders. We apply the empirical mode decomposition (EMD) analysis to quantify slow wave activity in electroencephalograms, and provide quantitative evidence to support our model. Based on this synchronization model, NREM sleep can be classified as SWS and non-SWS, such that NREM sleep can be considered as an intrinsically bistable process. Finally, we develop an automated algorithm for SWS classification. We show that this new approach can unify brain wave dynamics and their corresponding physiologic changes. |
format | Online Article Text |
id | pubmed-9076647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90766472022-05-08 Slow wave synchronization and sleep state transitions Guo, Dan Thomas, Robert J. Liu, Yanhui Shea, Steven A. Lu, Jun Peng, Chung-Kang Sci Rep Article Spontaneous synchronization over large networks is ubiquitous in nature, ranging from inanimate to biological systems. In the human brain, neuronal synchronization and de-synchronization occur during sleep, with the greatest degree of neuronal synchronization during slow wave sleep (SWS). The current sleep classification schema is based on electroencephalography and provides common criteria for clinicians and researchers to describe stages of non-rapid eye movement (NREM) sleep as well as rapid eye movement (REM) sleep. These sleep stage classifications have been based on convenient heuristic criteria, with little consideration of the accompanying normal physiological changes across those same sleep stages. To begin to resolve those inconsistencies, first focusing only on NREM sleep, we propose a simple cluster synchronization model to explain the emergence of SWS in healthy people without sleep disorders. We apply the empirical mode decomposition (EMD) analysis to quantify slow wave activity in electroencephalograms, and provide quantitative evidence to support our model. Based on this synchronization model, NREM sleep can be classified as SWS and non-SWS, such that NREM sleep can be considered as an intrinsically bistable process. Finally, we develop an automated algorithm for SWS classification. We show that this new approach can unify brain wave dynamics and their corresponding physiologic changes. Nature Publishing Group UK 2022-05-06 /pmc/articles/PMC9076647/ /pubmed/35523989 http://dx.doi.org/10.1038/s41598-022-11513-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Guo, Dan Thomas, Robert J. Liu, Yanhui Shea, Steven A. Lu, Jun Peng, Chung-Kang Slow wave synchronization and sleep state transitions |
title | Slow wave synchronization and sleep state transitions |
title_full | Slow wave synchronization and sleep state transitions |
title_fullStr | Slow wave synchronization and sleep state transitions |
title_full_unstemmed | Slow wave synchronization and sleep state transitions |
title_short | Slow wave synchronization and sleep state transitions |
title_sort | slow wave synchronization and sleep state transitions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076647/ https://www.ncbi.nlm.nih.gov/pubmed/35523989 http://dx.doi.org/10.1038/s41598-022-11513-0 |
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