[No authors listed]
BACKGROUND:This study was aimed to evaluate the association between interleukin-6 (IL-6) gene polymorphisms and the risk of hepatocellular carcinoma (HCC) in a meta-analysis. METHODS:A literature search was performed for case-control studies published during May, 1993 to May, 2020 focusing on IL-6 gene polymorphisms (-174Gâ>âC, -572Gâ>âC, and -597Gâ>âA) and HCC susceptibility by using PubMed, Cochrane Database, EMBASE, Web of science, and China National Knowledge Infrastructure. From 128 full-text articles, 11 were included in this meta-analysis. I index was used to assess heterogeneity and Newcastle-Ottawa Scale was utilized for quality assessment. RESULTS:For IL-6 -174Gâ>âC polymorphism, in codominant (GG vs CC: odds ratios [OR]â=â2.78, 95% confidence intervals [CI]â=â1.25-6.19, Pâ=â.01, Iâ=â16%) and recessive (GG+GC vs CC: ORâ=â2.76, 95% CIâ=â1.29-5.90, Pâ=â.009, Iâ=â3%) models, IL-6 -174G>C polymorphism was significantly associated with the risk of HCC. In dominant (GG vs CC+GC: ORâ=â1.80, 95% CIâ=â0.92-3.54, Pâ=â.09, Iâ=â86%) and allele (G vs C: ORâ=â1.49, 95% CIâ=â0.95-2.32, Pâ=â.08, Iâ=â68%) models, IL-6 -174G>C polymorphism had no impact on the risk of HCC. However, in non-Italian Caucasian population, IL-6 -174G>C polymorphism was significantly related to the occurrence of HCC in both dominant (GG vs CC+GC: ORâ=â3.26, 95% CIâ=â2.29-4.65, Pâ<â.00001, Iâ=â0%) and allele (G vs C: ORâ=â2.48, 95% CIâ=â1.48-4.15, Pâ=â.0006) models. Such correlations also could be observed when healthy individuals were selected as controls. For IL-6 -572G>C and -597G>A polymorphisms, no significant association was observed in all models, regardless of the source of control and population subgroups. No publication bias could be calculated when Begg and Egger tests were employed. CONCLUSION:This meta-analysis indicated that IL-6 -174G>C polymorphism was significantly related with the risk for HCC, especially in non-Italian Caucasian population. No significant association was observed for the correlation between IL-6 -572G>C and -597G>A polymorphisms and HCC susceptibility.
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