Shared and specific patterns of dynamic functional connectivity variability of striato-cortical circuitry in unmedicated bipolar and major depressive disorders

腹侧纹状体 纹状体 顶叶下小叶 中央前回 心理学 神经科学 辅助电机区 双相情感障碍 重性抑郁障碍 功能磁共振成像 扣带回前部 壳核 磁共振成像 医学 认知 多巴胺 放射科
作者
Guanmao Chen,Pan Chen,Jiaying Gong,Yanbin Jia,Shuming Zhong,Feng Chen,Jurong Wang,Zhenye Luo,Zhangzhang Qi,Li Huang,Ying Wang
出处
期刊:Psychological Medicine [Cambridge University Press]
卷期号:52 (4): 747-756 被引量:47
标识
DOI:10.1017/s0033291720002378
摘要

Abstract Background Accumulating studies have found structural and functional abnormalities of the striatum in bipolar disorder (BD) and major depressive disorder (MDD). However, changes in intrinsic brain functional connectivity dynamics of striato-cortical circuitry have not been investigated in BD and MDD. This study aimed to investigate the shared and specific patterns of dynamic functional connectivity (dFC) variability of striato-cortical circuitry in BD and MDD. Methods Brain resting-state functional magnetic resonance imaging data were acquired from 128 patients with unmedicated BD II (current episode depressed), 140 patients with unmedicated MDD, and 132 healthy controls (HCs). Six pairs of striatum seed regions were selected: the ventral striatum inferior (VSi) and the ventral striatum superior (VSs), the dorsal-caudal putamen (DCP), the dorsal-rostral putamen (DRP), and the dorsal caudate and the ventral-rostral putamen (VRP). The sliding-window analysis was used to evaluate dFC for each seed. Results Both BD II and MDD exhibited increased dFC variability between the left DRP and the left supplementary motor area, and between the right VRP and the right inferior parietal lobule. The BD II had specific increased dFC variability between the right DCP and the left precentral gyrus compared with MDD and HCs. The MDD had increased dFC variability between the left VSi and the left medial prefrontal cortex compared with BD II and HCs. Conclusions The patients with BD and MDD shared common dFC alteration in the dorsal striatal-sensorimotor and ventral striatal-cognitive circuitries. The patients with MDD had specific dFC alteration in the ventral striatal-affective circuitry.
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