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fMRI spectral signatures of sleep

Sleep can be distinguished from wake by changes in brain electrical activity, typically assessed using electroencephalography (EEG). The hallmark of nonrapid-eye-movement (NREM) sleep is the shift from high-frequency, low-amplitude wake EEG to low-frequency, high-amplitude sleep EEG dominated by spi...

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Autores principales: Song, Chen, Boly, Melanie, Tagliazucchi, Enzo, Laufs, Helmut, Tononi, Giulio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335231/
https://www.ncbi.nlm.nih.gov/pubmed/35862450
http://dx.doi.org/10.1073/pnas.2016732119
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author Song, Chen
Boly, Melanie
Tagliazucchi, Enzo
Laufs, Helmut
Tononi, Giulio
author_facet Song, Chen
Boly, Melanie
Tagliazucchi, Enzo
Laufs, Helmut
Tononi, Giulio
author_sort Song, Chen
collection PubMed
description Sleep can be distinguished from wake by changes in brain electrical activity, typically assessed using electroencephalography (EEG). The hallmark of nonrapid-eye-movement (NREM) sleep is the shift from high-frequency, low-amplitude wake EEG to low-frequency, high-amplitude sleep EEG dominated by spindles and slow waves. Here we identified signatures of sleep in brain hemodynamic activity, using simultaneous functional MRI (fMRI) and EEG. We found that, at the transition from wake to sleep, fMRI blood oxygen level–dependent (BOLD) activity evolved from a mixed-frequency pattern to one dominated by two distinct oscillations: a low-frequency (<0.1 Hz) oscillation prominent in light sleep and correlated with the occurrence of spindles, and a high-frequency oscillation (>0.1 Hz) prominent in deep sleep and correlated with the occurrence of slow waves. The two oscillations were both detectable across the brain but exhibited distinct spatiotemporal patterns. During the falling-asleep process, the low-frequency oscillation first appeared in the thalamus, then the posterior cortex, and lastly the frontal cortex, while the high-frequency oscillation first appeared in the midbrain, then the frontal cortex, and lastly the posterior cortex. During the waking-up process, both oscillations disappeared first from the thalamus, then the frontal cortex, and lastly the posterior cortex. The BOLD oscillations provide local signatures of spindle and slow wave activity. They may be employed to monitor the regional occurrence of sleep or wakefulness, track which regions are the first to fall asleep or wake up at the wake–sleep transitions, and investigate local homeostatic sleep processes.
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spelling pubmed-93352312022-07-30 fMRI spectral signatures of sleep Song, Chen Boly, Melanie Tagliazucchi, Enzo Laufs, Helmut Tononi, Giulio Proc Natl Acad Sci U S A Biological Sciences Sleep can be distinguished from wake by changes in brain electrical activity, typically assessed using electroencephalography (EEG). The hallmark of nonrapid-eye-movement (NREM) sleep is the shift from high-frequency, low-amplitude wake EEG to low-frequency, high-amplitude sleep EEG dominated by spindles and slow waves. Here we identified signatures of sleep in brain hemodynamic activity, using simultaneous functional MRI (fMRI) and EEG. We found that, at the transition from wake to sleep, fMRI blood oxygen level–dependent (BOLD) activity evolved from a mixed-frequency pattern to one dominated by two distinct oscillations: a low-frequency (<0.1 Hz) oscillation prominent in light sleep and correlated with the occurrence of spindles, and a high-frequency oscillation (>0.1 Hz) prominent in deep sleep and correlated with the occurrence of slow waves. The two oscillations were both detectable across the brain but exhibited distinct spatiotemporal patterns. During the falling-asleep process, the low-frequency oscillation first appeared in the thalamus, then the posterior cortex, and lastly the frontal cortex, while the high-frequency oscillation first appeared in the midbrain, then the frontal cortex, and lastly the posterior cortex. During the waking-up process, both oscillations disappeared first from the thalamus, then the frontal cortex, and lastly the posterior cortex. The BOLD oscillations provide local signatures of spindle and slow wave activity. They may be employed to monitor the regional occurrence of sleep or wakefulness, track which regions are the first to fall asleep or wake up at the wake–sleep transitions, and investigate local homeostatic sleep processes. National Academy of Sciences 2022-07-21 2022-07-26 /pmc/articles/PMC9335231/ /pubmed/35862450 http://dx.doi.org/10.1073/pnas.2016732119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Song, Chen
Boly, Melanie
Tagliazucchi, Enzo
Laufs, Helmut
Tononi, Giulio
fMRI spectral signatures of sleep
title fMRI spectral signatures of sleep
title_full fMRI spectral signatures of sleep
title_fullStr fMRI spectral signatures of sleep
title_full_unstemmed fMRI spectral signatures of sleep
title_short fMRI spectral signatures of sleep
title_sort fmri spectral signatures of sleep
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335231/
https://www.ncbi.nlm.nih.gov/pubmed/35862450
http://dx.doi.org/10.1073/pnas.2016732119
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