Polymorphisms in genes controlling inflammation and tissue repair in rheumatoid arthritis: a case control study

• Published in: BMC genetics 2011-03, Vol.12 (1), p.36-36, Article 36
• Main Authors: Emonts, Marieke, Hazes, Mieke J M W, Houwing-Duistermaat, Jeanine J, van der Gaast-de Jongh, Christa E, de Vogel, Lisette, Han, Huub K H, Wouters, Jacques M G W, Laman, Jon D, Dolhain, Radboud J E M
• Format: Article
• Language: English
• Subjects: Adult; Age of Onset; Aged; Apoptosis; Arthritis, Rheumatoid - genetics; Autoimmune diseases; Blood banks; Case-Control Studies; Cohort Studies; Design; Development and progression; Gene loci; Genetic aspects; Genetic polymorphisms; Genotype; Hospitals; Humans; Inflammation; Inflammation Mediators; Interleukin-8; Interleukin-8 - genetics; Male; Mediators; Medical statistics; Middle Aged; Pathogenesis; Pediatrics; Physiological aspects; Polymorphism, Genetic; Rheumatoid arthritis; Rheumatology; Severity of Illness Index; Tumor Necrosis Factor-alpha - genetics
• ISSN: 1471-2350; 1471-2156; 1471-2350; 1471-2156
• DOI: 10.1186/1471-2350-12-36

Various cytokines and inflammatory mediators are known to be involved in the pathogenesis of rheumatoid arthritis (RA). We hypothesized that polymorphisms in selected inflammatory response and tissue repair genes contribute to the susceptibility to and severity of RA. Polymorphisms in TNFA, IL1B, IL4, IL6, IL8, IL10, PAI1, NOS2a, C1INH, PARP, TLR2 and TLR4 were genotyped in 376 Caucasian RA patients and 463 healthy Caucasian controls using single base extension. Genotype distributions in patients were compared with those in controls. In addition, the association of polymorphisms with the need for anti-TNF-α treatment as a marker of RA severity was assessed. The IL8 781 CC genotype was associated with early onset of disease. The TNFA -238 G/A polymorphism was differentially distributed between RA patients and controls, but only when not corrected for age and gender. None of the polymorphisms was associated with disease severity. We here report an association between IL8 781 C/T polymorphism and age of onset of RA. Our findings indicate that there might be a role for variations in genes involved in the immune response and in tissue repair in RA pathogenesis. Nevertheless, additional larger genomic and functional studies are required to further define their role in RA.