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Association of cytokine gene polymorphisms and liver fibrosis in chronic hepatitis B
Author(s) -
Chan Henry LY,
Tse Ada ML,
Chim Angel ML,
Wong Vincent WS,
Choi Paul CL,
Yu Jun,
Zhang Mingdong,
Sung Joseph JY
Publication year - 2008
Publication title -
journal of gastroenterology and hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.214
H-Index - 130
eISSN - 1440-1746
pISSN - 0815-9319
DOI - 10.1111/j.1440-1746.2007.05110.x
Subject(s) - medicine , fibrosis , linkage disequilibrium , genotype , gastroenterology , odds ratio , cytokine , interleukin 1 receptor antagonist , immunology , haplotype , receptor antagonist , receptor , gene , biology , antagonist , genetics
Background and Aim: As liver fibrosis is the result of persistent necroinflammation in the liver, pro‐inflammatory cytokines secreted in response to cell injury have a central role in the pathogenesis of liver fibrosis. We aimed to investigate the association of cytokine gene polymorphism and liver fibrosis among Chinese patients with chronic hepatitis B. Methods: Polymorphisms at interleukin‐10 (IL‐10‐627, ‐1117), interleukin‐1‐beta (IL‐1β‐511, ‐31, ‐3964), interleukin‐1 receptor antagonist (IL‐1RN), and tumor necrosis factor‐alpha (TNF‐α‐308, ‐238) among Chinese chronic hepatitis B patients were determined. Severe liver fibrosis was defined as Ishak fibrosis score = 4 (of 6). Results: Fifty‐nine of 273 (22%) patients had severe fibrosis. The distribution of genotypes for IL‐10‐627 was CC (11%), CA (41%), and AA (48%). The CC genotype at IL‐10‐627 was protective against severe fibrosis (odds ratio (OR) 0.11; 95% CI 0.014–0.82; P = 0.032). After adjusted for baseline variables, the adjusted OR of CC genotypes at IL‐10‐627 for severe fibrosis was 0.063 (95% CI 0.06–0.64; P = 0.063). Other gene polymorphisms at IL‐1β, IL‐1RN, TNF‐α, and IL‐10 had no significant association with severe fibrosis. Weak linkage disequilibrium was observed between IL‐10‐627 and IL‐10‐1117 with linkage disequilibrium coefficient of 0.12 ( P < 0.001). The distribution of haplotypes of IL‐10‐1117 and IL‐10‐627 was A‐A (69%), A‐C (26%), and G‐C (5%). High and intermediate IL‐10 production (A‐C and G‐C) haplotypes were protective against severe fibrosis (OR 0.62; 95% CI 0.39–0.99; P = 0.046). Conclusions: High production genotype and haplotypes of IL‐10 were associated with less severe liver fibrosis in chronic hepatitis B in Chinese.