Abstract

Alterations in white matter (WM) microstructure have been implicated in the pathophysiology of major depressive disorder (MDD). However, previous findings have been inconsistent, partially due to low statistical power and the heterogeneity of depression. In the largest multi-site study to date, we examined WM anisotropy and diffusivity in 1305 MDD patients and 1602 healthy controls (age range 12–88 years) from 20 samples worldwide, which included both adults and adolescents, within the MDD Working Group of the Enhancing Neuroimaging Genetics through Meta-Analysis (ENIGMA) consortium. Processing of diffusion tensor imaging (DTI) data and statistical analyses were harmonized across sites and effects were meta-analyzed across studies. We observed subtle, but widespread, lower fractional anisotropy (FA) in adult MDD patients compared with controls in 16 out of 25 WM tracts of interest (Cohen’s d between 0.12 and 0.26). The largest differences were observed in the corpus callosum and corona radiata. Widespread higher radial diffusivity (RD) was also observed (all Cohen’s d between 0.12 and 0.18). Findings appeared to be driven by patients with recurrent MDD and an adult age of onset of depression. White matter microstructural differences in a smaller sample of adolescent MDD patients and controls did not survive correction for multiple testing. In this coordinated and harmonized multisite DTI study, we showed subtle, but widespread differences in WM microstructure in adult MDD, which may suggest structural disconnectivity in MDD.

Highlights

  • Major depressive disorder (MDD) is a debilitating and highly prevalent psychiatric disorder, characterized by depressed mood and loss of interest in daily activities [1]

  • After false discovery rate (FDR) correction, significantly lower fractional anisotropy (FA) was observed for adult MDD patients (N = 921; age range 22–88) compared to healthy controls (N = 1265) in 16 of the 25 ROIs, with the largest effects observed for the full white matter (WM) skeleton, followed by the anterior corona radiata (ACR), corona radiata (CR), corpus callosum (CC), genu of the corpus callosum (GCC), body of the corpus callosum (BCC) and anterior limb of the internal capsule (ALIC)

  • Lower FA was observed in the superior fronto-occipital fasciculus (SFO), sagittal stratum (SS), internal capsule (IC), posterior corona radiata (PCR), superior corona radiata (SCR), inferior fronto-occipital fasciculus (IFO), fornix/stria terminalis (FXST), external capsule (EC), and cingulate gyrus of the cingulum bundle (CGC) (Fig. 1, Supplementary Table S4 and Supplementary Fig. 1)

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Summary

Introduction

Major depressive disorder (MDD) is a debilitating and highly prevalent psychiatric disorder, characterized by depressed mood and loss of interest in daily activities [1]. In recent years, neuroimaging analyses have helped to characterize the neuroanatomical basis of MDD; consistent patterns of brain alterations have been difficult to identify due to limited power in previous studies and heterogeneity in data analysis. To address this issue, the MDD working group within the Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) consortium (http:// enigma.usc.edu/) initiated the largest coordinated metaanalyses of brain structure in MDD to date to investigate the robustness or consistency of neuroimaging findings across many samples worldwide. Our recent studies revealed lower hippocampal volume and altered cortical structure in MDD patients [3, 4]. Identifying patterns of alterations in WM in MDD could lead to the discovery of pathogenic processes and thereby guide development of new treatment targets for MDD; it could help provide ways of monitoring or predicting response to currently available treatments

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