Regional decreases of cortical thickness in major depressive disorder and their correlation with illness duration: a case-control study

Alterations in brain structure and function in major depressive disorder (MDD) have been identified in a number of studies, but findings regarding cortical thickness were various and inconsistent. Our current study aims to explore the differences in cortical thickness between individuals with MDD an...

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Published inFrontiers in psychiatry Vol. 15; p. 1297204
Main Authors Wang, Fukun, Hou, Xiaofang, Guo, Xiao, Zang, Chen, Wu, Gang, Zhao, Jingjing
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 2024
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Summary:Alterations in brain structure and function in major depressive disorder (MDD) have been identified in a number of studies, but findings regarding cortical thickness were various and inconsistent. Our current study aims to explore the differences in cortical thickness between individuals with MDD and healthy controls (HC) in a Chinese population. We investigated T1-weighted brain magnetic resonance imaging data from 61 participants (31 MDD and 30 HC). The cortical thickness between the two groups and analyzed correlations between cortical thickness and demographic variables in the MDD group for regions with significant between-group differences were conducted. Compared with the HC group, patients with MDD had significantly decreased cortical thickness, in left pars triangularis, left pars orbitalis, left rostral middle frontal gyrus, left supramarginal gyrus, right parahippocampal gyrus, right lingual gyrus, right fusiform and right inferior parietal gyrus. The cortical thickness of left rostral middle frontal gyrus was negatively correlated (  = -0.47,  = 0.028) with the illness duration in patients with MDD. Our study distinguished that cortical thickness decreases in numerous brain regions both in the left and right hemisphere in individuals with MDD, and the negative correlation between the cortical thickness of left rostral middle frontal gyrus illness duration. Our current findings are valuable in providing neural markers to identify MDD and understanding the potential pathophysiology of mood disorders.
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Edited by: Serdar M. Dursun, University of Alberta, Canada
Reviewed by: Luciana Ramalho Pimentel-Silva, State University of Campinas, Brazil
These authors have contributed equally to this work
Mateus Henrique Nogueira, State University of Campinas, Brazil
ISSN:1664-0640
1664-0640
DOI:10.3389/fpsyt.2024.1297204