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Sleep Architecture and Sleep EEG Alterations are Associated with Impaired Cognition Under Sleep Restriction

PURPOSE: Many studies have investigated the cognitive, emotional, and other impairments caused by sleep restriction. However, few studies have explored the relationship between cognitive performance and changes in sleep structure and electroencephalography (EEG) during sleep. The present study aimed...

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Autores principales: Mao, Tianxin, Chai, Ya, Guo, Bowen, Quan, Peng, Rao, Hengyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578164/
https://www.ncbi.nlm.nih.gov/pubmed/37850195
http://dx.doi.org/10.2147/NSS.S420650
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author Mao, Tianxin
Chai, Ya
Guo, Bowen
Quan, Peng
Rao, Hengyi
author_facet Mao, Tianxin
Chai, Ya
Guo, Bowen
Quan, Peng
Rao, Hengyi
author_sort Mao, Tianxin
collection PubMed
description PURPOSE: Many studies have investigated the cognitive, emotional, and other impairments caused by sleep restriction. However, few studies have explored the relationship between cognitive performance and changes in sleep structure and electroencephalography (EEG) during sleep. The present study aimed to examine whether changes in sleep structure and EEG can account for cognitive impairment caused by sleep restriction. PATIENTS AND METHODS: Sixteen young adults spent five consecutive nights (adaptation 9h, baseline 8h, 1st restriction 6h, 2nd restriction 6h, and recovery 10h) in a sleep laboratory, with polysomnography recordings taken during sleep. Throughout waking periods in each condition, participants completed the psychomotor vigilance test (PVT), which measures vigilant attention, and the Go/No-Go task, which measures inhibition control. RESULTS: The results showed that sleep restriction significantly decreased the proportion of N1 and N2 sleep, increased the proportion of N3 sleep, and reduced the time spent awake after sleep onset (WASO) and sleep onset latency. Poorer performance on the PVT and Go/No Go task was associated with longer WASO, a larger proportion of N3 sleep, and a smaller proportion of N2 sleep. Additionally, the power spectral density of delta waves significantly increased after sleep restriction, and this increase predicted a decrease in vigilance and inhibition control the next day. CONCLUSION: These findings suggest that sleep architecture and EEG signatures may partially explain cognitive impairment caused by sleep restriction.
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spelling pubmed-105781642023-10-17 Sleep Architecture and Sleep EEG Alterations are Associated with Impaired Cognition Under Sleep Restriction Mao, Tianxin Chai, Ya Guo, Bowen Quan, Peng Rao, Hengyi Nat Sci Sleep Original Research PURPOSE: Many studies have investigated the cognitive, emotional, and other impairments caused by sleep restriction. However, few studies have explored the relationship between cognitive performance and changes in sleep structure and electroencephalography (EEG) during sleep. The present study aimed to examine whether changes in sleep structure and EEG can account for cognitive impairment caused by sleep restriction. PATIENTS AND METHODS: Sixteen young adults spent five consecutive nights (adaptation 9h, baseline 8h, 1st restriction 6h, 2nd restriction 6h, and recovery 10h) in a sleep laboratory, with polysomnography recordings taken during sleep. Throughout waking periods in each condition, participants completed the psychomotor vigilance test (PVT), which measures vigilant attention, and the Go/No-Go task, which measures inhibition control. RESULTS: The results showed that sleep restriction significantly decreased the proportion of N1 and N2 sleep, increased the proportion of N3 sleep, and reduced the time spent awake after sleep onset (WASO) and sleep onset latency. Poorer performance on the PVT and Go/No Go task was associated with longer WASO, a larger proportion of N3 sleep, and a smaller proportion of N2 sleep. Additionally, the power spectral density of delta waves significantly increased after sleep restriction, and this increase predicted a decrease in vigilance and inhibition control the next day. CONCLUSION: These findings suggest that sleep architecture and EEG signatures may partially explain cognitive impairment caused by sleep restriction. Dove 2023-10-12 /pmc/articles/PMC10578164/ /pubmed/37850195 http://dx.doi.org/10.2147/NSS.S420650 Text en © 2023 Mao et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Mao, Tianxin
Chai, Ya
Guo, Bowen
Quan, Peng
Rao, Hengyi
Sleep Architecture and Sleep EEG Alterations are Associated with Impaired Cognition Under Sleep Restriction
title Sleep Architecture and Sleep EEG Alterations are Associated with Impaired Cognition Under Sleep Restriction
title_full Sleep Architecture and Sleep EEG Alterations are Associated with Impaired Cognition Under Sleep Restriction
title_fullStr Sleep Architecture and Sleep EEG Alterations are Associated with Impaired Cognition Under Sleep Restriction
title_full_unstemmed Sleep Architecture and Sleep EEG Alterations are Associated with Impaired Cognition Under Sleep Restriction
title_short Sleep Architecture and Sleep EEG Alterations are Associated with Impaired Cognition Under Sleep Restriction
title_sort sleep architecture and sleep eeg alterations are associated with impaired cognition under sleep restriction
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578164/
https://www.ncbi.nlm.nih.gov/pubmed/37850195
http://dx.doi.org/10.2147/NSS.S420650
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