Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci: e1002004

Epidemiology and candidate gene studies indicate a shared genetic basis for celiac disease (CD) and rheumatoid arthritis (RA), but the extent of this sharing has not been systematically explored. Previous studies demonstrate that 6 of the established non-HLA CD and RA risk loci (out of 26 loci for e...

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Veröffentlicht in:PLoS genetics 2011-02, Vol.7 (2)
Hauptverfasser: Zhernakova, Alexandra, Stahl, Eli A, Trynka, Gosia, Raychaudhuri, Soumya, Festen, Eleanora A, Franke, Lude, Westra, Harm-Jan, Fehrmann, Rudolf SN, Kurreeman, Fina AS, Thomson, Brian, Gupta, Namrata, Romanos, Jihane, McManus, Ross, Ryan, Anthony W, Turner, Graham, Brouwer, Elisabeth, Posthumus, Marcel D, Remmers, Elaine F, Tucci, Francesca, Toes, Rene, Grandone, Elvira, Mazzilli, Maria Cristina, Rybak, Anna, Cukrowska, Bozena, Coenen, Marieke JH, Radstake, R DJ, Riel, C Mvan, Li, Yonghong, Bakker, I Wde, Gregersen, Peter K, Worthington, Jane, Siminovitch, Katherine A, Klareskog, Lars, Huizinga, Tom WJ, Wijmenga, Cisca, Plenge, Robert M
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Sprache:eng
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Zusammenfassung:Epidemiology and candidate gene studies indicate a shared genetic basis for celiac disease (CD) and rheumatoid arthritis (RA), but the extent of this sharing has not been systematically explored. Previous studies demonstrate that 6 of the established non-HLA CD and RA risk loci (out of 26 loci for each disease) are shared between both diseases. We hypothesized that there are additional shared risk alleles and that combining genome-wide association study (GWAS) data from each disease would increase power to identify these shared risk alleles. We performed a meta-analysis of two published GWAS on CD (4,533 cases and 10,750 controls) and RA (5,539 cases and 17,231 controls). After genotyping the top associated SNPs in 2,169 CD cases and 2,255 controls, and 2,845 RA cases and 4,944 controls, 8 additional SNPs demonstrated P
ISSN:1553-7390
1553-7404
DOI:10.1371/journal.pgen.1002004