4.7 Article

Altered thalamic connectivity in insomnia disorder during wakefulness and sleep

期刊

HUMAN BRAIN MAPPING
卷 42, 期 1, 页码 259-270

出版社

WILEY
DOI: 10.1002/hbm.25221

关键词

EEG-fMRI; functional connectivity; hyperarousal; insomnia disorder; sleep misperception; thalamus

资金

  1. Beijing Brain Initiative of Beijing Municipal Science & Technology Commission [Z181100001518003]
  2. Beijing Municipal Natural Science Foundation [7172121]
  3. Beijing Municipal Science & Technology Commission [Z171100000117012, Z181100001518005]
  4. Guangdong Pearl River Talents Plan Innovative and Entrepreneurial Team [2016ZT06S220]
  5. National Key Research and Development Program of China [2017YFC0108900, 2018YFC2000603]
  6. National Natural Science Foundation of China [31421003, 81430037, 81671765, 81727808, 81771429, 81790650, 81790651, 81871427]
  7. Shenzhen Peacock Plan [KQTD2015033016104926]
  8. Shenzhen Science and Technology Research Funding Program [JCYJ20170412164413575]

向作者/读者索取更多资源

This study investigated brain functional networks of patients with insomnia disorder and healthy controls, revealing decreased thalamic connectivity in patients with insomnia disorder compared to controls, particularly with regions like the left amygdala and parahippocampal gyrus. Specific brain region connectivity was found to be significantly correlated with sleep misperception index, shedding new light on the neuropathophysiology of insomnia disorder.
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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