Sex differences of brain cortical structure in major depressive disorder

邦费罗尼校正 重性抑郁障碍 额中回 顶叶下小叶 额上回 析因分析 医学 中央前回 事后 颞中回 眶额皮质 听力学 脑回 心理学 内科学 神经科学 精神科 磁共振成像 放射科 前额叶皮质 认知 统计 数学
作者
Jingping Mou,Zheng Tian,Zhiliang Long,Lan Mei,Yuting Wang,Yifang Yuan,Xin Guo,Hai Yang,Xinyu Hu,Qiyong Gong,Li-Zhen Qiu
出处
期刊:Psychoradiology 卷期号:3
标识
DOI:10.1093/psyrad/kkad014
摘要

Abstract Background Major depressive disorder (MDD) has different clinical presentations in males and females. However, the neuroanatomical mechanisms underlying these sex differences are not fully understood. Objective The purpose of present study was to explore the sex differences in brain cortical thickness (CT) and surface area (SA) of MDD and the relationship between these differences and clinical manifestations in different gender. Methods High-resolution T1-weighted images were acquired from 61 patients with MDD and 61 healthy controls (36 females and 25 males, both). The sex differences in CT and SA were obtained using the FreeSurfer software and compared between every two groups by post hoc test. Spearman correlation analysis was also performed to explore the relationships between these regions and clinical characteristics. Results In male patients with MDD, the CT of the right precentral was thinner compared to female patients, although this did not survive Bonferroni correction. The SA of several regions, including right superior frontal, medial orbitofrontal gyrus, inferior frontal gyrus triangle, superior temporal, middle temporal, lateral occipital gyrus, and inferior parietal lobule in female patients with MDD was smaller than that in male patients (P < 0.01 after Bonferroni correction). In female patients, the SA of the right superior temporal (r = 0.438, P = 0.008), middle temporal (r = 0.340, P = 0.043), and lateral occipital gyrus (r = 0.372, P = 0.025) were positively correlated with illness duration. Conclusion The current study provides evidence of sex differences in CT and SA in patients with MDD, which may improve our understanding of the sex-specific neuroanatomical changes in the development of MDD.

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