Association between polymorphisms in the promoter region of interleukin-10 and susceptibility to inflammatory bowel disease

Springer Science and Business Media LLC - Tập 41 - Trang 1299-1310 - 2014
Hongchao Lv1,2, Yongshuai Jiang1,2, Jin Li1,2, Mingming Zhang1,2, Zhenwei Shang1,2, Jiajia Zheng1,2, Xin Wu1,2, Panpan Liu1,2, Ruijie Zhang1,2, Huimin Yu3,2
1College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, People’s Republic of China
2The Third Affiliated Hospital, Harbin Medical University, Harbin, People’s Republic of China
3Chinese Medicine Department of The 2nd Affiliated Hospital of Harbin Medical University, Harbin, People’s Republic of China

Tóm tắt

The aim of this study was to assess the association of polymorphisms in the promoter region of the IL-10 gene with the risk of inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC). Fifteen studies (3,693 cases and 4,574 controls) were included in a meta-analysis of association between IL-10 −1082G/A, −819C/T and −592C/A polymorphisms, and IBD, CD and UC using allele contrast and the recessive, dominant, and additive models. Hardy–Weinberg equilibrium was confirmed for each study. Heterogeneity and study quality were investigated using stratification analyses and sensitivity analyses. Polymorphism −1082G/A showed significant association with CD, with odds ratios (ORs) for the GG + GA genotype and GG versus AA genotype of 1.278 (1.004–1.627) and 1.238 (1.027–1.492) in all subjects. Significant associations were found in the Caucasian subgroup using the allele contrast, dominant, and additive models. C-allele carriers of the −819C/T polymorphism were at increased risk of IBD (OR 1.093, 95 % CI 1.004–1.190). Association with the −819C/T polymorphism was also found in Caucasians with CD (C vs. T: OR 1.104, 95 % CI 1.010–1.206; CC + CT vs. TT: OR 1.328, 95 % CI 1.006–1.754; CC vs. TT: OR 1.339, 95 % CI 1.008–1.778), and with UC (CC vs. CT + TT: OR 1.188, 95 % CI 1.019–1.385). No significant association was found between the −592C/A polymorphism and IBD, CD or UC. In conclusion, the meta-analysis demonstrated clear association between the IL-10 polymorphisms −1082G/A and −819C/T and the risk of IBD.

Tài liệu tham khảo

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