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

被引:73
作者
Yu, X.
Wieczorek, S. [2 ]
Franke, A. [3 ]
Yin, H. [4 ]
Pierer, M. [5 ]
Sina, C. [6 ]
Karlsen, T. H. [7 ]
Boberg, K. M. [7 ]
Bergquist, A. [8 ]
Kunz, M. [9 ]
Witte, T. [10 ]
Gross, W. L. [11 ]
Epplen, J. T. [2 ]
Alarcon-Riquelme, M. E. [4 ]
Schreiber, S. [3 ,6 ]
Ibrahim, S. M. [1 ]
机构
[1] Univ Rostock, Immunogenet Grp, Sect Immunogenet, D-18055 Rostock, Germany
[2] Ruhr Univ Bochum, Dept Human Genet, IGSN, Bochum, Germany
[3] Univ Kiel, Inst Clin Mol Biol, Kiel, Germany
[4] Uppsala Univ, Dept Gen & Pathol, Uppsala, Sweden
[5] Univ Leipzig, Dept Med 4, Leipzig, Germany
[6] Univ Kiel, Univ Hosp Schleswig Holstein, Dept Gen Internal Med, Kiel, Germany
[7] Univ Hosp, Rikshosp, Dept Med, Oslo, Norway
[8] Karolinska Univ Hosp, Dept Gastroenterol & Hepatol, Stockholm, Sweden
[9] Univ Rostock, Dermatol Clin, Rostock, Germany
[10] Hannover Med Sch, Dept Immunol & Rheumatol, D-3000 Hannover, Germany
[11] Univ Hosp Schleswig Holstein, Dept Rheumatol, Lubeck, Germany
关键词
mitochondria; chronic inflammatory diseases; uncoupling protein 2; UNCOUPLING PROTEIN-2; COMMON POLYMORPHISM; MULTIPLE-SCLEROSIS; PROMOTER; RISK; MICE;
D O I
10.1038/gene.2009.29
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. Genes and Immunity ( 2009) 10, 601-605; doi:10.1038/gene.2009.29; published online 23 April 2009
引用
收藏
页码:601 / 605
页数:5
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