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Cross-Disorder Analysis of Shared Genetic Components Between Cortical Structures and Major Psychiatric Disorders

重性抑郁障碍 双相情感障碍 精神分裂症(面向对象编程) 注意缺陷多动障碍 心理学 全基因组关联研究 双胞胎研究 自闭症谱系障碍 神经影像学 精神科 临床心理学 遗传力 自闭症 单核苷酸多态性 遗传学 认知 生物 基因型 基因
作者
Zongchang Li,David Li,Ying Hé,Kangli Wang,Xiaoqian Ma,Xiaogang Chen
出处
期刊:Schizophrenia Bulletin [Oxford University Press]
卷期号:48 (5): 1145-1154 被引量:3
标识
DOI:10.1093/schbul/sbac019
摘要

Abstract Background and Hypothesis Although large-scale neuroimaging studies have demonstrated similar patterns of structural brain abnormalities across major psychiatric disorders, the underlying genetic etiology behind these similar cross-disorder patterns is not well understood. Study Design We quantified the extent of shared genetic components between cortical structures and major psychiatric disorders (CS-MPD) by using genome-wide association study (GWAS) summary statistics of 70 cortical structures (surface area and thickness of the whole cortex and 34 cortical regions) and five major psychiatric disorders, consisting of attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD), bipolar disorder (BD), major depressive disorder (MDD), and schizophrenia (SCZ). Cross-disorder analyses were then conducted to estimate the degree of similarity in CS-MPD shared genetic components among these disorders. Study Results The CS-MPD shared genetic components have medium-to-strong positive correlations in ADHD, BD, MDD, and SCZ (r = 0.415 to r = 0.806) while ASD was significantly correlated with ADHD, BD, and SCZ (r = 0.388 to r = 0.403). These pairwise correlations of CS-MPD shared genetic components among disorders were significantly associated with corresponding cross-disorder similarities in cortical structural abnormalities (r = 0.668), accounting for 44% variance. In addition, one latent shared factor consisted primarily of BD, MDD, and SCZ, explaining 62.47% of the total variance in CS-MPD shared genetic components of all disorders. Conclusions The current results bridge the gap between shared cross-disorder heritability and shared structural brain abnormalities in major psychiatric disorders, providing important implications for a shared genetic basis of cortical structures in these disorders.

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