Literature DB >> 26922247

Enhanced default mode network connectivity with ventral striatum in subthreshold depression individuals.

J W Hwang1, S C Xin2, Y M Ou3, W Y Zhang4, Y L Liang5, J Chen6, X Q Yang7, X Y Chen8, T W Guo9, X J Yang2, W H Ma2, J Li2, B C Zhao2, Y Tu10, J Kong11.   

Abstract

Subthreshold depression (StD) is a highly prevalent condition associated with increased service utilization and social morbidity. Nevertheless, due to limitations in current diagnostic systems that set the boundary for major depressive disorder (MDD), very few brain imaging studies on the neurobiology of StD have been carried out, and its underlying neurobiological mechanism remains unclear. In recent years, accumulating evidence suggests that the disruption of the default mode network (DMN), a network involved in self-referential processing, affective cognition, and emotion regulation, is involved in major depressive disorder. Using independent component analysis, we investigated resting-state default mode network (DMN) functional connectivity (FC) changes in two cohorts of StD patients with different age ranges (young and middle-aged, n = 57) as well as matched controls (n = 79). We found significant FC increase between the DMN and ventral striatum (key region in the reward network), in both cohorts of StD patients in comparison with controls. In addition, we also found the FC between the DMN and ventral striatum was positively and significantly associated with scores on the Center for Epidemiologic Studies Depression Scale (CES-D), a measurement of depressive symptomatology. We speculate that this enhanced FC between the DMN and the ventral striatum may reflect a self-compensation to ameliorate the lowered reward function.
Copyright © 2016 The Authors. Published by Elsevier Ltd.. All rights reserved.

Entities:  

Keywords:  Default mode network; Independent component analysis; Resting-state functional connectivity; Subthreshold depression; Ventral striatum; fMRI

Mesh:

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Year:  2016        PMID: 26922247      PMCID: PMC4838997          DOI: 10.1016/j.jpsychires.2016.02.005

Source DB:  PubMed          Journal:  J Psychiatr Res        ISSN: 0022-3956            Impact factor:   4.791


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