4.7 Article

Shared genetic etiology between anxiety disorders and psychiatric and related intermediate phenotypes

期刊

PSYCHOLOGICAL MEDICINE
卷 50, 期 4, 页码 692-704

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S003329171900059X

关键词

Anxiety disorder; genetic correlation; genome-wide association study; intermediate phenotype; linkage disequilibrium score regression; major depressive disorder

向作者/读者索取更多资源

BackgroundPsychiatric disorders and related intermediate phenotypes are highly heritable and have a complex, overlapping polygenic architecture. A large-scale genome-wide association study (GWAS) of anxiety disorders identified genetic variants that are significant on a genome-wide. The current study investigated the genetic etiological overlaps between anxiety disorders and frequently cooccurring psychiatric disorders and intermediate phenotypes.MethodsUsing case-control and factor score models, we investigated the genetic correlations of anxiety disorders with eight psychiatric disorders and intermediate phenotypes [the volumes of seven subcortical brain regions, childhood cognition, general cognitive ability and personality traits (subjective well-being, loneliness, neuroticism and extraversion)] from large-scale GWASs (n = 7556-298 420) by linkage disequilibrium score regression.ResultsAmong psychiatric disorders, the risk of anxiety disorders was positively genetically correlated with the risks of major depressive disorder (MDD) (r(g) standard error = 0.83 +/- 0.16, p = 1.97 x 10(-7)), schizophrenia (SCZ) (0.28 +/- 0.09, p = 1.10 x 10(-3)) and attention-deficit/hyperactivity disorder (ADHD) (0.34 +/- 0.13, p = 8.40 x 10(-3)). Among intermediate phenotypes, significant genetic correlations existed between the risk of anxiety disorders and neuroticism (0.81 +/- 0.17, p = 1.30 x 10(-6)), subjective well-being (-0.73 +/- 0.18, p = 4.89 x 10(-5)), general cognitive ability (-0.23 +/- 0.08, p = 4.70 x 10(-3)) and putamen volume (-0.50 +/- 0.18, p = 5.00 x 10(-3)). No other significant genetic correlations between anxiety disorders and psychiatric or intermediate phenotypes were observed (p > 0.05). The case-control model yielded stronger genetic effect sizes than the factor score model.ConclusionsOur findings suggest that common genetic variants underlying the risk of anxiety disorders contribute to elevated risks of MDD, SCZ, ADHD and neuroticism and reduced quality of life, putamen volume and cognitive performance. We suggest that the comorbidity of anxiety disorders is partly explained by common genetic variants.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据