Abstract

Background: There is an urgent need for a meta-analysis that characterizes the brain states of major depression disorder (MDD) patients and potentially provides reliable biomarkers, because heterogeneity in the results of resting-state functional neuroimaging has been observed between studies, with some patients not showing the consistent changes, or even opposite patterns. Thus, we evaluated consistent regional brain activity alterations in medication-naive patients with first-episode unipolar MDD and compared the results with those in healthy controls (HCs).Methods: A systematic database search was conducted (in PubMed, Ovid, and Web of Knowledge) between January 1984 and July 2016 to select resting-state functional activity studies with a voxel-wise analysis in MDD. We used anisotropic effect size-signed differential mapping to perform a whole-brain meta-analysis, comparing functional alterations between first-episode medication-naive unipolar MDD patients and HCs by integrating the studies. In addition, subgroup meta-analysis was conducted to control for the MRI analysis method. Moreover, the meta-regression analyses were performed to examine the potential effects of mean age, education duration, illness duration, and severity of depressive symptoms.Results: A total of 12 studies were included, comparing 313 MDD patients with 283 HCs. The pooled and subgroup meta-analysis found that the MDD patients showed hyperactivity in the left parahippocampal gyrus, left supplementary motor area, left amygdala, left hippocampus, and left middle frontal gyrus (MFG; orbital part), and hypoactivity in the left lingual gyrus, left middle occipital gyrus, right cuneus cortex, right MFG (orbital part), and left cerebellum. In the meta-regression analyses, the mean illness duration was positively associated with hyper-activation in the left parahippocampal gyrus and hypoactivation in the hemispheric lobule IV/V of the left cerebellum.Conclusions: This meta-analysis indicated that MDD patients had significant and robust resting-state brain activity alteration in amygdala, left hippocampus and other regions, which implicated this finding in the pathophysiology of cognitive and emotional impairment in MDD patients.

Highlights

  • Depressive disorders constitute a common group of psychiatric disorders with high prevalence (Rosenstrom and Jokela, 2017)

  • The results of the present meta-analysis are largely consistent with previous major depressive disorder (MDD) studies, showing a subset of regional differences, including hyperactive left PHG, left supplementary motor area (SMA), left middle frontal gyrus (MFG), and hypoactive left lingual gyrus (LING), left middle occipital gyrus (MOG), right CUN cortex, right MFG, right supramarginal gyrus (SMAR), and right postcentral gyrus (PoCG)

  • The results of the present study suggest that the left hippocampus, with reduced volume and hyperactivity in depression, could serve as a neuroimaging biomarker for diagnosing MDD

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Summary

Introduction

Depressive disorders constitute a common group of psychiatric disorders with high prevalence (Rosenstrom and Jokela, 2017). Recent studies have investigated depressive disorder at the level of individual symptoms that define major depressive disorder (MDD) (Fried and Nesse, 2015). The current MDD diagnosis depends on subjective symptoms, experiences and perceptions, requiring the presence of at least one of the two core symptoms: (1) depressed mood and/or (2) markedly diminished interest or pleasure in all, or almost all, activities (Rosenstrom and Jokela, 2017). There is an urgent need for a meta-analysis that characterizes the brain states of major depression disorder (MDD) patients and potentially provides reliable biomarkers, because heterogeneity in the results of resting-state functional neuroimaging has been observed between studies, with some patients not showing the consistent changes, or even opposite patterns. We evaluated consistent regional brain activity alterations in medication-naive patients with first-episode unipolar MDD and compared the results with those in healthy controls (HCs)

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