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Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis
Authors:Hüffmeier Ulrike  Uebe Steffen  Ekici Arif B  Bowes John  Giardina Emiliano  Korendowych Eleanor  Juneblad Kristina  Apel Maria  McManus Ross  Ho Pauline  Bruce Ian N  Ryan Anthony W  Behrens Frank  Lascorz Jesús  Böhm Beate  Traupe Heiko  Lohmann Jörg  Gieger Christian  Wichmann Heinz-Erich  Herold Christine  Steffens Michael  Klareskog Lars  Wienker Thomas F  Fitzgerald Oliver  Alenius Gerd-Marie  McHugh Neil J  Novelli Giuseppe  Burkhardt Harald  Barton Anne  Reis André
Institution:Institute of Human Genetics, University of Erlangen-Nuremberg, Erlangen, Germany.
Abstract:Psoriatic arthritis (PsA) is an inflammatory joint disease that is distinct from other chronic arthritides and which is frequently accompanied by psoriasis vulgaris (PsV) and seronegativity for rheumatoid factor. We conducted a genome-wide association study in 609 German individuals with PsA (cases) and 990 controls with replication in 6 European cohorts including a total of 5,488 individuals. We replicated PsA associations at HLA-C and IL12B and identified a new association at TRAF3IP2 (rs13190932, P = 8.56 × 10?1?). TRAF3IP2 was also associated with PsV in a German cohort including 2,040 individuals (rs13190932, P = 1.95 × 10?3). Sequencing of the exons of TRAF3IP2 identified a coding variant (p.Asp10Asn, rs33980500) as the most significantly associated SNP (P = 1.13 × 10?2?, odds ratio = 1.95). Functional assays showed reduced binding of this TRAF3IP2 variant to TRAF6, suggesting altered modulation of immunoregulatory signals through altered TRAF interactions as a new and shared pathway for PsA and PsV.
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