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Global and local complexity of intracranial EEG decreases during NREM sleep

Key to understanding the neuronal basis of consciousness is the characterization of the neural signatures of changes in level of consciousness during sleep. Here we analysed three measures of dynamical complexity on spontaneous depth electrode recordings from 10 epilepsy patients during wakeful rest...

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Autores principales: Schartner, Michael M, Pigorini, Andrea, Gibbs, Steve A, Arnulfo, Gabriele, Sarasso, Simone, Barnett, Lionel, Nobili, Lino, Massimini, Marcello, Seth, Anil K, Barrett, Adam B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007155/
https://www.ncbi.nlm.nih.gov/pubmed/30042832
http://dx.doi.org/10.1093/nc/niw022
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author Schartner, Michael M
Pigorini, Andrea
Gibbs, Steve A
Arnulfo, Gabriele
Sarasso, Simone
Barnett, Lionel
Nobili, Lino
Massimini, Marcello
Seth, Anil K
Barrett, Adam B
author_facet Schartner, Michael M
Pigorini, Andrea
Gibbs, Steve A
Arnulfo, Gabriele
Sarasso, Simone
Barnett, Lionel
Nobili, Lino
Massimini, Marcello
Seth, Anil K
Barrett, Adam B
author_sort Schartner, Michael M
collection PubMed
description Key to understanding the neuronal basis of consciousness is the characterization of the neural signatures of changes in level of consciousness during sleep. Here we analysed three measures of dynamical complexity on spontaneous depth electrode recordings from 10 epilepsy patients during wakeful rest (WR) and different stages of sleep: (i) Lempel–Ziv complexity, which is derived from how compressible the data are; (ii) amplitude coalition entropy, which measures the variability over time of the set of channels active above a threshold; (iii) synchrony coalition entropy, which measures the variability over time of the set of synchronous channels. When computed across sets of channels that are broadly distributed across multiple brain regions, all three measures decreased substantially in all participants during early-night non-rapid eye movement (NREM) sleep. This decrease was partially reversed during late-night NREM sleep, while the measures scored similar to WR during rapid eye movement (REM) sleep. This global pattern was in almost all cases mirrored at the local level by groups of channels located in a single region. In testing for differences between regions, we found elevated signal complexity in the frontal lobe. These differences could not be attributed solely to changes in spectral power between conditions. Our results provide further evidence that the level of consciousness correlates with neural dynamical complexity.
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spelling pubmed-60071552018-07-24 Global and local complexity of intracranial EEG decreases during NREM sleep Schartner, Michael M Pigorini, Andrea Gibbs, Steve A Arnulfo, Gabriele Sarasso, Simone Barnett, Lionel Nobili, Lino Massimini, Marcello Seth, Anil K Barrett, Adam B Neurosci Conscious Research Article Key to understanding the neuronal basis of consciousness is the characterization of the neural signatures of changes in level of consciousness during sleep. Here we analysed three measures of dynamical complexity on spontaneous depth electrode recordings from 10 epilepsy patients during wakeful rest (WR) and different stages of sleep: (i) Lempel–Ziv complexity, which is derived from how compressible the data are; (ii) amplitude coalition entropy, which measures the variability over time of the set of channels active above a threshold; (iii) synchrony coalition entropy, which measures the variability over time of the set of synchronous channels. When computed across sets of channels that are broadly distributed across multiple brain regions, all three measures decreased substantially in all participants during early-night non-rapid eye movement (NREM) sleep. This decrease was partially reversed during late-night NREM sleep, while the measures scored similar to WR during rapid eye movement (REM) sleep. This global pattern was in almost all cases mirrored at the local level by groups of channels located in a single region. In testing for differences between regions, we found elevated signal complexity in the frontal lobe. These differences could not be attributed solely to changes in spectral power between conditions. Our results provide further evidence that the level of consciousness correlates with neural dynamical complexity. Oxford University Press 2017-01-25 /pmc/articles/PMC6007155/ /pubmed/30042832 http://dx.doi.org/10.1093/nc/niw022 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Schartner, Michael M
Pigorini, Andrea
Gibbs, Steve A
Arnulfo, Gabriele
Sarasso, Simone
Barnett, Lionel
Nobili, Lino
Massimini, Marcello
Seth, Anil K
Barrett, Adam B
Global and local complexity of intracranial EEG decreases during NREM sleep
title Global and local complexity of intracranial EEG decreases during NREM sleep
title_full Global and local complexity of intracranial EEG decreases during NREM sleep
title_fullStr Global and local complexity of intracranial EEG decreases during NREM sleep
title_full_unstemmed Global and local complexity of intracranial EEG decreases during NREM sleep
title_short Global and local complexity of intracranial EEG decreases during NREM sleep
title_sort global and local complexity of intracranial eeg decreases during nrem sleep
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007155/
https://www.ncbi.nlm.nih.gov/pubmed/30042832
http://dx.doi.org/10.1093/nc/niw022
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