Suppr超能文献

对122341例欧洲血统个体的主要焦虑症进行全基因组关联研究,确定了58个基因座并突出了γ-氨基丁酸能信号传导。

Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling.

作者信息

Strom Nora I, Verhulst Brad, Bacanu Silviu-Alin, Cheesman Rosa, Purves Kirstin L, Gedik Hüseyin, Mitchell Brittany L, Kwong Alex S, Faucon Annika B, Singh Kritika, Medland Sarah, Colodro-Conde Lucia, Krebs Kristi, Hoffmann Per, Herms Stefan, Gehlen Jan, Ripke Stephan, Awasthi Swapnil, Palviainen Teemu, Tasanko Elisa M, Peterson Roseann E, Adkins Daniel E, Shabalin Andrey A, Adams Mark J, Iveson Matthew H, Campbell Archie, Thomas Laurent F, Winsvold Bendik S, Drange Ole Kristian, Børte Sigrid, Ter Kuile Abigail R, Nguyen Tan-Hoang, Meier Sandra M, Corfield Elizabeth C, Hannigan Laurie, Levey Daniel F, Czamara Darina, Weber Heike, Choi Karmel W, Pistis Giorgio, Couvy-Duchesne Baptiste, Van der Auwera Sandra, Teumer Alexander, Karlsson Robert, Garcia-Argibay Miguel, Lee Donghyung, Wang Rujia, Bjerkeset Ottar, Stordal Eystein, Bäckmann Julia, Salum Giovanni A, Zai Clement C, Kennedy James L, Zai Gwyneth, Tiwari Arun K, Heilmann-Heimbach Stefanie, Schmidt Börge, Kaprio Jaakko, Kennedy Martin M, Boden Joseph, Havdahl Alexandra, Middeldorp Christel M, Lopes Fabiana L, Akula Nirmala, McMahon Francis J, Binder Elisabeth B, Fehm Lydia, Ströhle Andreas, Castelao Enrique, Tiemeier Henning, Stein Dan J, Whiteman David, Olsen Catherine, Fuller Zachary, Wang Xin, Wray Naomi R, Byrne Enda M, Lewis Glyn, Timpson Nicholas J, Davis Lea K, Hickie Ian B, Gillespie Nathan A, Milani Lili, Schumacher Johannes, Woldbye David P, Forstner Andreas J, Nöthen Markus M, Hovatta Iiris, Horwood John, Copeland William E, Maes Hermine H, McIntosh Andrew M, Andreassen Ole A, Zwart John-Anker, Mors Ole, Børglum Anders D, Mortensen Preben B, Ask Helga, Reichborn-Kjennerud Ted, Najman Jackob M, Stein Murray B, Gelernter Joel, Milaneschi Yuri, Penninx Brenda W, Boomsma Dorret I, Maron Eduard, Erhardt-Lehmann Angelika, Rück Christian, Kircher Tilo T, Melzig Christiane A, Alpers Georg W, Arolt Volker, Domschke Katharina, Smoller Jordan W, Preisig Martin, Martin Nicholas G, Lupton Michelle K, Luik Annemarie I, Reif Andreas, Grabe Hans J, Larsson Henrik, Magnusson Patrik K, Oldehinkel Albertine J, Hartman Catharina A, Breen Gerome, Docherty Anna R, Coon Hilary, Conrad Rupert, Lehto Kelli, Deckert Jürgen, Eley Thalia C, Mattheisen Manuel, Hettema John M

机构信息

Department of Psychology, Humboldt-Universität zu Berlin, Berlin, Germany.

Institute of Psychiatric Phenomics and Genomics (IPPG), University Hospital, LMU Munich, Munich, Germany.

出版信息

medRxiv. 2024 Jul 5:2024.07.03.24309466. doi: 10.1101/2024.07.03.24309466.

Abstract

The major anxiety disorders (ANX; including generalized anxiety disorder, panic disorder, and phobias) are highly prevalent, often onset early, persist throughout life, and cause substantial global disability. Although distinct in their clinical presentations, they likely represent differential expressions of a dysregulated threat-response system. Here we present a genome-wide association meta-analysis comprising 122,341 European ancestry ANX cases and 729,881 controls. We identified 58 independent genome-wide significant ANX risk variants and 66 genes with robust biological support. In an independent sample of 1,175,012 self-report ANX cases and 1,956,379 controls, 51 of the 58 associated variants were replicated. As predicted by twin studies, we found substantial genetic correlation between ANX and depression, neuroticism, and other internalizing phenotypes. Follow-up analyses demonstrated enrichment in all major brain regions and highlighted GABAergic signaling as one potential mechanism underlying ANX genetic risk. These results advance our understanding of the genetic architecture of ANX and prioritize genes for functional follow-up studies.

摘要

主要焦虑症(ANX;包括广泛性焦虑症、惊恐障碍和恐惧症)非常普遍,通常起病早,终生持续,并在全球范围内导致严重的残疾。尽管它们在临床表现上有所不同,但可能代表了失调的威胁反应系统的不同表现形式。在此,我们呈现了一项全基因组关联荟萃分析,该分析纳入了122341例欧洲血统的ANX病例和729881例对照。我们鉴定出58个独立的全基因组显著ANX风险变异以及66个有充分生物学支持的基因。在一个由1175012例自我报告的ANX病例和1956379例对照组成的独立样本中,58个相关变异中的51个得到了重复验证。正如双胞胎研究所预测的,我们发现ANX与抑郁症、神经质及其他内化表型之间存在显著的遗传相关性。后续分析表明在所有主要脑区均有富集,并突出了GABA能信号传导作为ANX遗传风险的一种潜在机制。这些结果推进了我们对ANX遗传结构的理解,并为功能后续研究确定了优先研究的基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/11245051/5aa6f2865037/nihpp-2024.07.03.24309466v1-f0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验