Functional connectivity strengths in unmedicated patients with major depressive disorder: a resting-state functional magnetic resonance imaging study
10.3760/cma.j.issn.1006-7884.2017.05.012
- VernacularTitle:抑郁症未治疗患者静息态脑功能连接强度的研究
- Author:
Guanmao CHEN
1
;
Lianping ZHAO
;
Yanbin JIA
;
Shuming ZHONG
;
Zhangzhang QI
;
Shunkai LAI
;
Yao SUN
;
Li HUANG
;
Ying WANG
Author Information
1. 暨南大学附属第一医院影像中心, 广州,510630
- Publication Type:Journal Article
- Keywords:
Depressive disorder;
Resting state;
Functional connectivity strengths
- From:
Chinese Journal of Psychiatry
2017;50(5):377-382
- CountryChina
- Language:Chinese
-
Abstract:
Objective To provide a new approach to further elucidate the underlying pathogenesis of major depressive disorder by using resting-state functional connectivity strengths(FCS) in unmedicated patients with major depressive disorder(MDD). Methods Thirty-three unmedicated patients with MDD and thirty-three normal controls underwent the resting-state functional magnetic resonance imaging(rs-fMRI). After preprocessing of rs-fMRI, the whole brain FCS values were constructed. Two-sample t-test was used to compare the FCS values of both groups to locate the regions with significant change. And correlation analysis was performed between the FCS values extracted from significantly different brain regions and Hamilton Depression Scale (HAMD24) scores. Results One sample t test had shown that high FCS values brain areas (hubs) of MDD patients and normal controls were mainly located in the default mode network (the prefrontal cortex, anterior cingulate gyrus, posterior cingulate gyrus, precuneus/cuneus, angular gyrus) and parietal cortex, lateral temporal cortex as well as occipital cortex. In comparison to the normal controls, the MDD patients had FCS values significantly decreased in the bilateral posterior cerebellar lobe (right posterior cerebellar t=-4.57, P<0.05;left posterior cerebellar t=-3.40,P<0.05), and FCS values increased in the right superior temporal gyrus (t=3.71,P<0.05) and left anterior insular lobe (t=3.91, P<0.05). There were no significant correlations between the HAMD24 scores and the FCS values in right/left posterior cerebellar (r=0.081, P=0.654; r=-0.028, P=0.877), right superior temporal gyrus (r=0.211, P=0.239) and left anterior insular lobe (r=-0.017,P=0.924). Conclusions These findings suggest abnormal functional connectivity in the bilateral posterior cerebellar lobe, right temporal lobe and left insular lobe in MDD. The FCS analysis may be used as a new research method to explore the pathogenesis of MDD.