| Literature DB >> 31740837 |
Max Lam1,2,3,4,5,6, Chia-Yen Chen4,5,7,8,9, Zhiqiang Li10,11, Alicia R Martin4,5,7, Julien Bryois12, Xixian Ma13, Helena Gaspar14, Masashi Ikeda15, Beben Benyamin16,17,18, Brielin C Brown19,20, Ruize Liu4,5, Wei Zhou11,21, Lili Guan22,23,24, Yoichiro Kamatani25,26, Sung-Wan Kim27, Michiaki Kubo28, Agung A A A Kusumawardhani29, Chih-Min Liu30,31, Hong Ma22,23,24, Sathish Periyasamy32,33, Atsushi Takahashi26,34, Zhida Xu35, Hao Yu22,23,24, Feng Zhu36,37,38, Wei J Chen30,31,39, Stephen Faraone40, Stephen J Glatt41, Lin He11,42,43, Steven E Hyman5,44, Hai-Gwo Hwu30,31,39, Steven A McCarroll5,45, Benjamin M Neale4,5,7, Pamela Sklar46, Dieter B Wildenauer47, Xin Yu22,23,24, Dai Zhang22,23,24, Bryan J Mowry32,33, Jimmy Lee48, Peter Holmans49, Shuhua Xu13,50,51,52, Patrick F Sullivan53, Stephan Ripke4,5,54, Michael C O'Donovan49, Mark J Daly4,5,7,55, Shengying Qin11,56, Pak Sham57,58, Nakao Iwata15, Kyung S Hong59, Sibylle G Schwab60,61, Weihua Yue62,63,64,65, Ming Tsuang66, Jianjun Liu67,68, Xiancang Ma69,70,71, René S Kahn72,73,74, Yongyong Shi75,76,77,78, Hailiang Huang79,80,81.
Abstract
Schizophrenia is a debilitating psychiatric disorder with approximately 1% lifetime risk globally. Large-scale schizophrenia genetic studies have reported primarily on European ancestry samples, potentially missing important biological insights. Here, we report the largest study to date of East Asian participants (22,778 schizophrenia cases and 35,362 controls), identifying 21 genome-wide-significant associations in 19 genetic loci. Common genetic variants that confer risk for schizophrenia have highly similar effects between East Asian and European ancestries (genetic correlation = 0.98 ± 0.03), indicating that the genetic basis of schizophrenia and its biology are broadly shared across populations. A fixed-effect meta-analysis including individuals from East Asian and European ancestries identified 208 significant associations in 176 genetic loci (53 novel). Trans-ancestry fine-mapping reduced the sets of candidate causal variants in 44 loci. Polygenic risk scores had reduced performance when transferred across ancestries, highlighting the importance of including sufficient samples of major ancestral groups to ensure their generalizability across populations.Entities:
Mesh:
Year: 2019 PMID: 31740837 PMCID: PMC6885121 DOI: 10.1038/s41588-019-0512-x
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330