焦虑症和精神疾病广泛遗传重叠的新基因座的鉴定。

Markos Tesfaye, Piotr Jaholkowski, Alexey A Shadrin, Dennis van der Meer, Guy F L Hindley, Børge Holen, Nadine Parker, Pravesh Parekh, Viktoria Birkenæs, Zillur Rahman, Shahram Bahrami, Gleda Kutrolli, Oleksandr Frei, Srdjan Djurovic, Anders M Dale, Olav B Smeland, Kevin S O'Connell, Ole A Andreassen
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背景:焦虑症普遍存在,焦虑症状往往与精神疾病同时发生。在这里,我们旨在确定与焦虑相关的基因组风险基因座,描述其遗传结构,以及与精神疾病的遗传重叠。方法:我们使用了焦虑(GAD-2评分)、精神分裂症、双相情感障碍、重度抑郁症和注意力缺陷多动障碍(ADHD)的最大可用GWAS。我们使用MiXeR和LAVA来表征表型之间的遗传结构和遗传重叠。此外,还进行了条件和联合错误发现率分析,以促进对与焦虑相关的基因组基因座和与精神疾病共有的基因座的识别。分别使用OpenTargets和FUMA进行基因注释和基因集分析。结果:焦虑是多基因的,估计有8.4k个遗传风险变异,并与精神疾病广泛重叠(4.1-7.8k个变异)。MiXeR和LAVA都显示焦虑和精神障碍之间主要存在正的遗传相关性。我们通过对精神障碍的条件调节,确定了154个焦虑位点(139个新位点)。我们确定了焦虑与重度抑郁症(n=66)、双相情感障碍(n=19)、精神分裂症(n=51)和多动症(n=37)之间的共同基因座。与共享基因座注释的基因相比,注释到焦虑基因座的基因在更广泛的生物途径中表现出富集,并在更多样的组织中表现出不同的组织表达。结论:焦虑是一种高度多基因表型,与精神疾病有广泛的基因重叠。这些基因重叠使得能够识别焦虑症的新基因座和精神疾病的共享基因座。共享的遗传结构可能是焦虑共病的基础,而已确定的遗传基因座暗示了可能成为潜在药物靶点的分子途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Identification of Novel Genomic Loci for Anxiety and Extensive Genetic Overlap with Psychiatric Disorders.

Background: Anxiety disorders are prevalent and anxiety symptoms co-occur with many psychiatric disorders. We aimed to identify genomic risk loci associated with anxiety, characterize its genetic architecture, and genetic overlap with psychiatric disorders.

Methods: We used the GWAS of anxiety symptoms, schizophrenia, bipolar disorder, major depression, and attention deficit hyperactivity disorder (ADHD). We employed MiXeR and LAVA to characterize the genetic architecture and genetic overlap between the phenotypes. Conditional and conjunctional false discovery rate analyses were performed to boost the identification of genomic loci associated with anxiety and those shared with psychiatric disorders. Gene annotation and gene set analyses were conducted using OpenTargets and FUMA, respectively.

Results: Anxiety was polygenic with 12.9k estimated genetic risk variants and overlapped extensively with psychiatric disorders (4.1-11.4k variants). MiXeR and LAVA revealed predominantly positive genetic correlations between anxiety and psychiatric disorders. We identified 114 novel loci for anxiety by conditioning on the psychiatric disorders. We also identified loci shared between anxiety and major depression (n = 47), bipolar disorder (n = 33), schizophrenia (n = 71), and ADHD (n = 20). Genes annotated to anxiety loci exhibit enrichment for a broader range of biological pathways and differential tissue expression in more diverse tissues than those annotated to the shared loci.

Conclusions: Anxiety is a highly polygenic phenotype with extensive genetic overlap with psychiatric disorders. These genetic overlaps enabled the identification of novel loci for anxiety. The shared genetic architecture may underlie the extensive cross-disorder comorbidity of anxiety, and the identified genetic loci implicate molecular pathways that may lead to potential drug targets.

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