Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

Nalls, Mike A., Pankratz, Nathan, Lill, Christina M., Do, Chuong B., Hernandez, Dena G., Saad, Mohamad, DeStefano, Anita L., Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F., Arepalli, Sampath, Letson, Christopher, Edsall, Connor, Stefansson, Hreinn, Liu, Xinmin, Pliner, Hannah, Lee, Joseph H., Cheng, Rong, Ikram, M. Arfan, Ioannidis, John P. A., Hadjigeorgiou, Georgios M., Bis, Joshua C., Martinez, Maria, Perlmutter, Joel S., Goate, Alison, Marder, Karen, Fiske, Brian, Sutherland, Margaret, Xiromerisiou, Georgia, Myers, Richard H., Clark, Lorraine N., Stefansson, Kari, Hardy, John A., Heutink, Peter, Chen, Honglei, Wood, Nicholas W., Houlden, Henry, Payami, Haydeh, Brice, Alexis, Scott, William K., Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, Singleton, Andrew B., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Morris, Huw 2014. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nature Genetics 46 (9) , pp. 989-993. 10.1038/ng.3043

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Abstract

We conducted a meta-analysis of Parkinson's disease genome-wide association studies using a common set of 7,893,274 variants across 13,708 cases and 95,282 controls. Twenty-six loci were identified as having genome-wide significant association; these and 6 additional previously reported loci were then tested in an independent set of 5,353 cases and 5,551 controls. Of the 32 tested SNPs, 24 replicated, including 6 newly identified loci. Conditional analyses within loci showed that four loci, including GBA, GAK-DGKQ, SNCA and the HLA region, contain a secondary independent risk variant. In total, we identified and replicated 28 independent risk variants for Parkinson's disease across 24 loci. Although the effect of each individual locus was small, risk profile analysis showed substantial cumulative risk in a comparison of the highest and lowest quintiles of genetic risk (odds ratio (OR) = 3.31, 95% confidence interval (CI) = 2.55–4.30; P = 2 × 10−16). We also show six risk loci associated with proximal gene expression or DNA methylation.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Medicine MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG)
Subjects:	R Medicine > R Medicine (General)
Additional Information:	International Parkinson's Disease Genomics Consortium (IPDGC), Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI), 23andMe, GenePD, NeuroGenetics Research Consortium (NGRC), Hussman Institute of Human Genomics (HIHG), The Ashkenazi Jewish Dataset Investigator, Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE), North American Brain Expression Consortium (NABEC), United Kingdom Brain Expression Consortium (UKBEC), Greek Parkinson's Disease Consortium, Alzheimer Genetic Analysis Group,
Publisher:	Nature
ISSN:	1061-4036
Date of Acceptance:	30 June 2014
Last Modified:	28 Oct 2022 09:51
URI:	https://orca.cardiff.ac.uk/id/eprint/75924

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