EEG microstates are correlated with brain functional networks during slow-wave sleep.


Journal

NeuroImage
ISSN: 1095-9572
Titre abrégé: Neuroimage
Pays: United States
ID NLM: 9215515

Informations de publication

Date de publication:
15 07 2020
Historique:
received: 23 10 2019
revised: 02 04 2020
accepted: 03 04 2020
pubmed: 11 4 2020
medline: 26 2 2021
entrez: 11 4 2020
Statut: ppublish

Résumé

Electroencephalography (EEG) microstates have been extensively studied in wakefulness and have been described as the "atoms of thought". Previous studies of EEG have found four microstates, i.e., microstates A, B, C and D, that are consistent among participants across the lifespan during the resting state. Studies using simultaneous EEG and functional magnetic resonance imaging (fMRI) have provided evidence for correlations between EEG microstates and fMRI networks during the resting state. Microstates have also been found during non-rapid eye movement (NREM) sleep. Slow-wave sleep (SWS) is considered the most restorative sleep stage and has been associated with the maintenance of sleep. However, the relationship between EEG microstates and brain functional networks during SWS has not yet been investigated. In this study, simultaneous EEG-fMRI data were collected during SWS to test the correspondence between EEG microstates and fMRI networks. EEG microstate-informed fMRI analysis revealed that three out of the four microstates showed significant correlations with fMRI data: 1) fMRI fluctuations in the insula and posterior temporal gyrus positively correlated with microstate B, 2) fMRI signals in the middle temporal gyrus and fusiform gyrus negatively correlated with microstate C, and 3) fMRI fluctuations in the occipital lobe negatively correlated with microstate D, while fMRI signals in the anterior cingulate and cingulate gyrus positively correlated with this microstate. Functional brain networks were then assessed using group independent component analysis based on the fMRI data. The group-level spatial correlation analysis showed that the fMRI auditory network overlapped the fMRI activation map of microstate B, the executive control network overlapped the fMRI deactivation of microstate C, and the visual and salience networks overlapped the fMRI deactivation and activation maps of microstate D. In addition, the subject-level spatial correlations between the general linear model (GLM) beta map of each microstate and the individual maps of each component yielded by dual regression also showed that EEG microstates were closely associated with brain functional networks measured using fMRI during SWS. Overall, the results showed that EEG microstates were closely related to brain functional networks during SWS, which suggested that EEG microstates provide an important electrophysiological basis underlying brain functional networks.

Identifiants

pubmed: 32276057
pii: S1053-8119(20)30273-1
doi: 10.1016/j.neuroimage.2020.116786
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

116786

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.

Auteurs

Jing Xu (J)

Laboratory of Applied Brain and Cognitive Sciences, Shanghai International Studies University, Shanghai, China.

Yu Pan (Y)

Laboratory of Applied Brain and Cognitive Sciences, Shanghai International Studies University, Shanghai, China.

Shuqin Zhou (S)

Center for MRI Research, Peking University, Beijing, China; Department of Biomedical Engineering, College of Engineering, Peking University, Beijing, China.

Guangyuan Zou (G)

Center for MRI Research, Peking University, Beijing, China; Beijing City Key Lab for Medical Physics and Engineering, Institution of Heavy Ion Physics, School of Physics, Peking University, Beijing, China.

Jiayi Liu (J)

Center for MRI Research, Peking University, Beijing, China; Beijing City Key Lab for Medical Physics and Engineering, Institution of Heavy Ion Physics, School of Physics, Peking University, Beijing, China.

Zihui Su (Z)

Nuffield Department of Clinical Neurosciences, Oxford University, Oxford, United Kingdom.

Qihong Zou (Q)

Center for MRI Research, Peking University, Beijing, China. Electronic address: zouqihong@pku.edu.cn.

Jia-Hong Gao (JH)

Laboratory of Applied Brain and Cognitive Sciences, Shanghai International Studies University, Shanghai, China; Center for MRI Research, Peking University, Beijing, China; Beijing City Key Lab for Medical Physics and Engineering, Institution of Heavy Ion Physics, School of Physics, Peking University, Beijing, China; McGovern Institute for Brain Research, Peking University, Beijing, Beijing, China. Electronic address: jgao@pku.edu.cn.

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