Reduced resting‐state functional connectivity and sleep impairment in abstinent male alcohol‐dependent patients. Issue 17 (4th August 2019)

• Record Type: Journal Article
• Authors: Liu, Jingjing; Cai, Wanye; Zhao, Meng; Cai, Wenlong; Sui, Feng; Hou, Wenbao; Wang, Hongde; Yu, Dahua; Yuan, Kai
• Is Part Of: Human brain mapping. Volume 40:Issue 17(2019)
• Page Start: 4941
• Page End: 4951
• Publication Date: 2019-08-04
• Subjects: alcohol dependence -- resting‐state functional connectivity -- sleep impairment -- thalamus; Brain mapping -- Periodicals; 611.81
• DOI: 10.1002/hbm.24749
• Languages: English
• ISSNs: 1065-9471

Abstract

Abstract: Alcohol dependence is associated with poor sleep quality, which has both been implicated with thalamocortical circuits function. To identify the possible roles of these circuits in the alcohol‐sleep association, we investigated the volume of both left and right thalamus and corresponding resting‐state functional connectivity (RSFC) differences between 15 alcohol‐dependent patients (AD) and 15 healthy controls (HC) male participants. The neuroimaging findings were then correlated with clinical variables, that is, Alcohol Use Disorders Identification Test (AUDIT) and Pittsburgh Sleep Quality Index (PSQI). Additionally, mediation analysis was carried out to test whether the thalamocortical RSFC mediates the relationship between drinking behavior and sleep impairments in AD when applicable. We observed a significant positive correlation between AUDIT score and PSQI score in AD. Compared with HC, AD showed reduced RSFC between the left thalamus and medial prefrontal cortex (mPFC), orbitofrontal cortex, anterior cingulate cortex (ACC), and right caudate. We also observed a negative correlation between RSFC of the left thalamus–mPFC and PSQI score in AD. More importantly, the left thalamus–mPFC RSFC strength mediated the relationship between AUDIT score and PSQI score in AD. No significant difference was detected in the normalized volume of both left and right thalamus, and volumes were not significantly correlated with clinical variables. Our results demonstrate that AD show abnormal interactions within thalamocortical circuits in association with drinking behaviors and sleep impairments. It is hoped that our study focusing on thalamocortical circuits could provide new information on potential novel therapeutic targets for treatment of sleep impairment in alcohol‐dependent patients.