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Abnormal functional connectivity in the habenula is associated with subjective hyperarousal state in chronic insomnia disorder

BACKGROUND: The hyperarousal process model plays a central role in the physiology of chronic insomnia disorder (CID). Recent evidence has demonstrated that the habenula is involved in the arousal and sleep–wake cycle. However, whether the intrinsic habenular functional network contributes to the und...

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Autores principales: Gong, Liang, Cheng, Fang, Li, Xue, Wang, Zhiqi, Wang, Shuo, Xu, Ronghua, Zhang, Bei, Xi, Chunhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10426801/
https://www.ncbi.nlm.nih.gov/pubmed/37588671
http://dx.doi.org/10.3389/fneur.2023.1119595
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author Gong, Liang
Cheng, Fang
Li, Xue
Wang, Zhiqi
Wang, Shuo
Xu, Ronghua
Zhang, Bei
Xi, Chunhua
author_facet Gong, Liang
Cheng, Fang
Li, Xue
Wang, Zhiqi
Wang, Shuo
Xu, Ronghua
Zhang, Bei
Xi, Chunhua
author_sort Gong, Liang
collection PubMed
description BACKGROUND: The hyperarousal process model plays a central role in the physiology of chronic insomnia disorder (CID). Recent evidence has demonstrated that the habenula is involved in the arousal and sleep–wake cycle. However, whether the intrinsic habenular functional network contributes to the underlying mechanism of CID and its relationship to the arousal state in CID remains unclear. METHODS: This single-centered study included 34 patients with subjective CID and 22 matched good sleep control (GSC), and underwent a series of neuropsychological tests and resting-state functional magnetic resonance imaging scans. The habenular functional network was assessed using seed-based functional connectivity (FC) analysis. The subjective arousal state was evaluated with the hyperarousal scale (HAS). Alterations in the habenular FC network and their clinical significance in patients with CID were explored. RESULTS: Compared with the GSC group, the CID group showed decreased habenular FC in the left caudate nucleus and right inferior parietal lobule and increased FC in the right habenula, bilateral calcarine cortex, and posterior cingulate cortex. The decreased FC between the left habenula and caudate nucleus was associated with an increased arousal state in the CID group. CONCLUSION: The present results provide evidence for a dysfunctional habenular network in patients with CID. These findings extend our understanding of the neuropathological mechanisms underlying the hyperarousal model in chronic insomnia.
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spelling pubmed-104268012023-08-16 Abnormal functional connectivity in the habenula is associated with subjective hyperarousal state in chronic insomnia disorder Gong, Liang Cheng, Fang Li, Xue Wang, Zhiqi Wang, Shuo Xu, Ronghua Zhang, Bei Xi, Chunhua Front Neurol Neurology BACKGROUND: The hyperarousal process model plays a central role in the physiology of chronic insomnia disorder (CID). Recent evidence has demonstrated that the habenula is involved in the arousal and sleep–wake cycle. However, whether the intrinsic habenular functional network contributes to the underlying mechanism of CID and its relationship to the arousal state in CID remains unclear. METHODS: This single-centered study included 34 patients with subjective CID and 22 matched good sleep control (GSC), and underwent a series of neuropsychological tests and resting-state functional magnetic resonance imaging scans. The habenular functional network was assessed using seed-based functional connectivity (FC) analysis. The subjective arousal state was evaluated with the hyperarousal scale (HAS). Alterations in the habenular FC network and their clinical significance in patients with CID were explored. RESULTS: Compared with the GSC group, the CID group showed decreased habenular FC in the left caudate nucleus and right inferior parietal lobule and increased FC in the right habenula, bilateral calcarine cortex, and posterior cingulate cortex. The decreased FC between the left habenula and caudate nucleus was associated with an increased arousal state in the CID group. CONCLUSION: The present results provide evidence for a dysfunctional habenular network in patients with CID. These findings extend our understanding of the neuropathological mechanisms underlying the hyperarousal model in chronic insomnia. Frontiers Media S.A. 2023-07-31 /pmc/articles/PMC10426801/ /pubmed/37588671 http://dx.doi.org/10.3389/fneur.2023.1119595 Text en Copyright © 2023 Gong, Cheng, Li, Wang, Wang, Xu, Zhang and Xi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Gong, Liang
Cheng, Fang
Li, Xue
Wang, Zhiqi
Wang, Shuo
Xu, Ronghua
Zhang, Bei
Xi, Chunhua
Abnormal functional connectivity in the habenula is associated with subjective hyperarousal state in chronic insomnia disorder
title Abnormal functional connectivity in the habenula is associated with subjective hyperarousal state in chronic insomnia disorder
title_full Abnormal functional connectivity in the habenula is associated with subjective hyperarousal state in chronic insomnia disorder
title_fullStr Abnormal functional connectivity in the habenula is associated with subjective hyperarousal state in chronic insomnia disorder
title_full_unstemmed Abnormal functional connectivity in the habenula is associated with subjective hyperarousal state in chronic insomnia disorder
title_short Abnormal functional connectivity in the habenula is associated with subjective hyperarousal state in chronic insomnia disorder
title_sort abnormal functional connectivity in the habenula is associated with subjective hyperarousal state in chronic insomnia disorder
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10426801/
https://www.ncbi.nlm.nih.gov/pubmed/37588671
http://dx.doi.org/10.3389/fneur.2023.1119595
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