Altered thalamic connectivity in insomnia disorder during wakefulness and sleep.
Altered thalamic connectivity in insomnia disorder during wakefulness and sleep.
复制标题
失眠症在清醒和睡眠期间丘脑连接的改变
DOI:
10.1002/hbm.25221
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发表时间:
2021-01
影响因子:
4.8
通讯作者:
Gao JH
中科院分区:
文献类型:
--
作者:
Zou G;Li Y;Liu J;Zhou S;Xu J;Qin L;Shao Y;Yao P;Sun H;Zou Q;Gao JH
Insomnia disorder is the most common sleep disorder and has drawn increasing attention. Many studies have shown that hyperarousal plays a key role in the pathophysiology of insomnia disorder. However, the specific brain mechanisms underlying insomnia disorder remain unclear. To elucidate the neuropathophysiology of insomnia disorder, we investigated the brain functional networks of patients with insomnia disorder and healthy controls across the sleep–wake cycle. EEG‐fMRI data from 33 patients with insomnia disorder and 31 well‐matched healthy controls during wakefulness and nonrapid eye movement sleep, including N1, N2 and N3 stages, were analyzed. A medial and anterior thalamic region was selected as the seed considering its role in sleep–wake regulation. The functional connectivity between the thalamic seed and voxels across the brain was calculated. ANOVA with factors “group” and “stage” was performed on thalamus‐based functional connectivity. Correlations between the misperception index and altered functional connectivity were explored. A group‐by‐stage interaction was observed at widespread cortical regions. Regarding the main effect of group, patients with insomnia disorder demonstrated decreased thalamic connectivity with the left amygdala, parahippocampal gyrus, putamen, pallidum and hippocampus across wakefulness and all three nonrapid eye movement sleep stages. The thalamic connectivity in the subcortical cluster and the right temporal cluster in N1 was significantly correlated with the misperception index. This study demonstrated the brain functional basis in insomnia disorder and illustrated its relationship with sleep misperception, shedding new light on the brain mechanisms of insomnia disorder and indicating potential therapeutic targets for its treatment.
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DOI:
10.1016/j.nicl.2017.07.008
发表时间:
2017
期刊:
NeuroImage. Clinical
影响因子:
--
作者:
Bagshaw AP;Hale JR;Campos BM;Rollings DT;Wilson RS;Alvim MKM;Coan AC;Cendes F
通讯作者:
Cendes F
DOI:
10.1523/jneurosci.1809-08.2008
发表时间:
2008-10-01
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
Cano G;Mochizuki T;Saper CB
通讯作者:
Saper CB
影响因子:
5.6
作者:
Hsiao, Fan-Chi;Tsai, Pei-Jung;Wu, Yu-Zu
通讯作者:
Wu, Yu-Zu
影响因子:
5.7
作者:
Hale, Joanne R.;White, Thomas P.;Bagshaw, Andrew P.
通讯作者:
Bagshaw, Andrew P.
影响因子:
5.7
作者:
Falahpour M;Chang C;Wong CW;Liu TT
通讯作者:
Liu TT