Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL.

Authors:
Eva Ellinghaus, Philip E Stuart, David Ellinghaus, Rajan P Nair, Sophie Debrus, John V Raelson, Majid Belouchi, Trilokraj Tejasvi, Yanming Li, Lam C Tsoi, Anna T Onken, Tonu Esko, Andres Metspalu, Proton Rahman, Dafna D Gladman, Anne M Bowcock, Cynthia Helms, Gerald G Krueger, Sulev Koks, Külli Kingo, Christian Gieger, H Erich Wichmann, Ulrich Mrowietz, Stephan Weidinger, Stefan Schreiber, Gonçalo R Abecasis, James T Elder, Michael Weichenthal, Andre Franke
Year of publication:
2012
Volume:
132
Issue:
4
Issn:
0022-202X
Journal title abbreviated:
J INVEST DERMATOL
Journal title long:
Journal of investigative dermatology
Impact factor:
6.915
Abstract: 
Psoriatic arthritis (PsA) is a chronic inflammatory musculoskeletal disease affecting up to 30% of psoriasis vulgaris (PsV) cases and approximately 0.25 to 1% of the general population. To identify common susceptibility loci, we performed a meta-analysis of three imputed genome-wide association studies (GWAS) on psoriasis, stratified for PsA. A total of 1,160,703 single-nucleotide polymorphisms (SNPs) were analyzed in the discovery set consisting of 535 PsA cases and 3,432 controls from Germany, the United States, and Canada. We followed up two SNPs in 1,931 PsA cases and 6,785 controls comprising six independent replication panels from Germany, Estonia, the United States, and Canada. In the combined analysis, a genome-wide significant association was detected at 2p16 near the REL locus encoding c-Rel (rs13017599, P=1.18 × 10(-8), odds ratio (OR)=1.27, 95% confidence interval (CI)=1.18-1.35). The rs13017599 polymorphism is known to associate with rheumatoid arthritis (RA), and another SNP near REL (rs702873) was recently implicated in PsV susceptibility. However, conditional analysis indicated that rs13017599, rather than rs702873, accounts for the PsA association at REL. We hypothesize that c-Rel, as a member of the Rel/NF-κB family, is associated with PsA in the context of disease pathways that involve other identified PsA and PsV susceptibility genes including TNIP1, TNFAIP3, and NFκBIA.