| Literature DB >> 28011712 |
Jia Nee Foo1,2, Louis C Tan3, Ishak D Irwan2, Wing-Lok Au3, Hui Qi Low2, Kumar-M Prakash3, Azlina Ahmad-Annuar4, Jinxin Bei5, Anne Yy Chan6, Chiung Mei Chen7, Yi-Chun Chen7, Sun Ju Chung8, Hao Deng9, Shen-Yang Lim10, Vincent Mok6, Hao Pang11, Zhong Pei12, Rong Peng13, Hui-Fang Shang13, Kyuyoung Song14, Ai Huey Tan10, Yih-Ru Wu7, Tin Aung15,16, Ching-Yu Cheng15,16,17, Fook Tim Chew18, Soo-Hong Chew19, Siow-Ann Chong20, Richard P Ebstein21, Jimmy Lee17,20, Seang-Mei Saw15,16,17,22, Adeline Seow22, Mythily Subramaniam20, E-Shyong Tai23, Eranga N Vithana15,16,17, Tien-Yin Wong15,16,17, Khai Koon Heng2, Wee-Yang Meah2, Chiea Chuen Khor2,15,24, Hong Liu25, Furen Zhang25, Jianjun Liu2, Eng-King Tan3,17.
Abstract
Genome-wide association studies (GWAS) on Parkinson's disease (PD) have mostly been done in Europeans and Japanese. No study has been done in Han Chinese, which make up nearly a fifth of the world population. We conducted the first Han Chinese GWAS analysing a total of 22,729 subjects (5,125 PD cases and 17,604 controls) from Singapore, Hong Kong, Malaysia, Korea, mainland China and Taiwan. We performed imputation, merging and logistic regression analyses of 2,402,394 SNPs passing quality control filters in 779 PD cases, 13,227 controls, adjusted for the first three principal components. 90 SNPs with association P < 10-4 were validated in 9 additional sample collections and the results were combined using fixed-effects inverse-variance meta-analysis. We observed strong associations reaching genome-wide significance at SNCA, LRRK2 and MCCC1, confirming their important roles in both European and Asian PD. We also identified significant (P < 0.05) associations at 5 loci (DLG2, SIPA1L2, STK39, VPS13C and RIT2), and observed the same direction of associations at 9 other loci including BST1 and PARK16. Allelic heterogeneity was observed at LRRK2 while European risk SNPs at 6 other loci including MAPT and GBA-SYT11 were non-polymorphic or very rare in our cohort. Overall, we replicate associations at SNCA, LRRK2, MCCC1 and 14 other European PD loci but did not identify Asian-specific loci with large effects (OR > 1.45) on PD risk. Our results also demonstrate some differences in the genetic contribution to PD between Europeans and Asians. Further pan-ethnic meta-analysis with European GWAS cohorts may unravel new PD loci.Entities:
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Year: 2017 PMID: 28011712 DOI: 10.1093/hmg/ddw379
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150