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Association of UCP2 −866 G/A polymorphism with chronic inflammatory diseases

2009; Springer Nature; Volume: 10; Issue: 6 Linguagem: Inglês

10.1038/gene.2009.29

1476-5470

Xinhua Yu, Stefan Wieczorek, André Franke, Haiyan Yin, Matthias Pierer, Christian Sina, Tom H. Karlsen, Kirsten Muri Boberg, Annika Bergquist, Manfred Kunz, T Witte, W. L. Gross, Jörg T. Epplen, Marta E. Alarcón‐Riquelme, Stefanie Schreiber, Saleh Ibrahim,

ATP Synthase and ATPases Research

We reported earlier that two mitochondrial gene polymorphisms, UCP2 –866 G/A (rs659366) and mtDNA nt13708 G/A (rs28359178), are associated with multiple sclerosis (MS). Here we aim to investigate whether these functional polymorphisms contribute to other eight chronic inflammatory diseases, including rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), Wegener' granulomatosis (WG), Churg–Strauss syndrome (CSS), Crohn's disease (CD), ulcerative colitis (UC), primary sclerosing cholangitis (PSC) and psoriasis. Compared with individual control panels, the UCP2 –866 G/A polymorphism was associated with RA and SLE, and the mtDNA nt13708 G/A polymorphism with RA. Compared with combined controls, the UCP2 –866 G/A polymorphism was associated with SLE, WG, CD and UC. When all eight disease panels and the original MS panel were combined in a meta-analysis, the UCP2 was associated with chronic inflammatory diseases in terms of either alleles (odds ratio (OR)=0.91, 95% confidence interval (95% CI): 0.86–0.96), P=0.0003) or genotypes (OR=0.88, (95% CI: 0.82–0.95), P=0.0008), with the –866A allele associated with a decreased risk to diseases. As the −866A allele increases gene expression, our findings suggest a protective role of the UCP2 protein in chronic inflammatory diseases.