| Literature DB >> 24080174 |
Eleanna Kara1, Georgia Xiromerisiou, Cleanthe Spanaki, Maria Bozi, Georgios Koutsis, Marios Panas, Efthimios Dardiotis, Styliani Ralli, Jose Bras, Christopher Letson, Connor Edsall, Hannah Pliner, Sampath Arepalli, Kallirhoe Kalinderi, Liana Fidani, Sevasti Bostantjopoulou, Margaux F Keller, Nicholas W Wood, John Hardy, Henry Houlden, Leonidas Stefanis, Andreas Plaitakis, Dena Hernandez, Georgios M Hadjigeorgiou, Mike A Nalls, Andrew B Singleton.
Abstract
Genome-wide association studies (GWAS) have been shown to be a powerful approach to identify risk loci for neurodegenerative diseases. Recent GWAS in Parkinson's disease (PD) have been successful in identifying numerous risk variants pointing to novel pathways potentially implicated in the pathogenesis of PD. Contributing to these GWAS efforts, we performed genotyping of previously identified risk alleles in PD patients and control subjects from Greece. We showed that previously published risk profiles for Northern European and American populations are also applicable to the Greek population. In addition, although our study was largely underpowered to detect individual associations, we replicated 5 of 32 previously published risk variants with nominal p values <0.05. Genome-wide complex trait analysis revealed that known risk loci explain disease risk in 1.27% of Greek PD patients. Collectively, these results indicate that there is likely a substantial genetic component to PD in Greece, similarly to other worldwide populations, that remains to be discovered. Published by Elsevier Inc.Entities:
Keywords: GCTA; GWAS; Genetics; Greece; Parkinson's disease; Risk profiles
Mesh:
Year: 2013 PMID: 24080174 PMCID: PMC3830580 DOI: 10.1016/j.neurobiolaging.2013.07.011
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673