CARD8 p.C10X polymorphism is associated with inflammatory activity in early rheumatoid arthritis. Issue 4 (13th May 2009)

• Record Type: Journal Article
• Authors: Kastbom, Alf; Johansson, Martin; Verma, Deepti; Söderkvist, Peter; Rantapää-Dahlqvist, Solbritt
• Is Part Of: Annals of the rheumatic diseases. Volume 69:Issue 4(2010)
• Page Start: 723
• Page End: 726
• Publication Date: 2009-05-13
• Subjects: Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/ard.2008.106989
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Objectives: CARD8 and NLRP3 are constituents of the inflammasome which regulates interleukin 1β production. The influence of polymorphisms in CARD8 and NLRP3 on rheumatoid arthritis (RA) susceptibility and severity were evaluated. Methods: CARD8 p.C10X and NLRP3 p.Q705K genotypes were assessed in >500 controls and patients with early RA from northern Sweden. The patients were monitored regularly over a 2–year period. The 28-joint disease activity score (DAS28) and its separate components were compared across genotypes. Results: Patients with one or more variant alleles in CARD8 (CARD8-X) had increased DAS28, tender joint count and erythrocyte sedimentation rate during the 2-year follow-up period despite receiving disease-modifying antirheumatic drugs to a greater extent. CARD8-X was significantly over-represented among patients who received anti-tumour necrosis factor therapy during the first 2 years. CARD8 and NLRP3 genotypes did not influence radiological joint damage and were not associated with an increased susceptibility. Conclusions: Carriage of CARD8-X is associated with a worse disease course in early RA.