重性抑郁障碍
扣带回前部
扁桃形结构
灰质
基于体素的形态计量学
海马结构
脑岛
心理学
扣带皮质
医学
神经科学
磁共振成像
精神科
内科学
白质
中枢神经系统
放射科
认知
作者
Mirjam Stratmann,Carsten Konrad,Harald Kugel,Axel Krug,Sonja Schöning,Patricia Ohrmann,Christina Uhlmann,Christian Postert,Thomas Suslow,Walter Heindel,Volker Arolt,Tilo Kircher,Udo Dannlowski
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2014-07-22
卷期号:9 (7): e102692-e102692
被引量:148
标识
DOI:10.1371/journal.pone.0102692
摘要
Background Major depressive disorder is a serious psychiatric illness with a highly variable and heterogeneous clinical course. Due to the lack of consistent data from previous studies, the study of morphometric changes in major depressive disorder is still a major point of research requiring additional studies. The aim of the study presented here was to characterize and quantify regional gray matter abnormalities in a large sample of clinically well-characterized patients with major depressive disorder. Methods For this study one-hundred thirty two patients with major depressive disorder and 132 age- and gender-matched healthy control participants were included, 35 with their first episode and 97 with recurrent depression. To analyse gray matter abnormalities, voxel-based morphometry (VBM8) was employed on T1 weighted MRI data. We performed whole-brain analyses as well as a region-of-interest approach on the hippocampal formation, anterior cingulate cortex and amygdala, correlating the number of depressive episodes. Results Compared to healthy control persons, patients showed a strong gray-matter reduction in the right anterior insula. In addition, region-of-interest analyses revealed significant gray-matter reductions in the hippocampal formation. The observed alterations were more severe in patients with recurrent depressive episodes than in patients with a first episode. The number of depressive episodes was negatively correlated with gray-matter volume in the right hippocampus and right amygdala. Conclusions The anterior insula gray matter structure appears to be strongly affected in major depressive disorder and might play an important role in the neurobiology of depression. The hippocampal and amygdala volume loss cumulating with the number of episodes might be explained either by repeated neurotoxic stress or alternatively by higher relapse rates in patients showing hippocampal atrophy.
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