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No association between hOGG1 Ser326Cys polymorphism and hepatocellular carcinoma

机译:hOGG1 Ser326Cys多态性与肝细胞癌无关联

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Background/Aims: To clarify any association between the hOGG1 Ser326Cys polymorphism and susceptibility to hepatocellular carcinoma (HCC). Methodology: The PubMed, CNKI databases were searched for all available articles. The OR corresponding to the 95% confidence interval (95% CI) was used to assess the association between hOGG1 Ser326Cys polymorphism and susceptibility to HCC. Results: Seven case-control studies, with 1,663 cases and 1,675 controls, were available for this analysis. No association was found between hOGG1 Ser326Cys polymorphism and HCC risk (dominant model: OR=0.695, 95% CI: 0.501-0.964, p=0.029; additive model: OR=0.682, 95% CI: 0.374-1.245, p=0.213; recessive model: OR=1.215, 95% CI: 0.711-2.078, p=0.476). Sensitivity analysis did not perturb the results. Conclusions: These findings indicated that hOGG1 Ser326Cys polymorphism may not play a role in HCC development. However, larger scale studies are needed for confirmation.
机译:背景/目的:阐明hOGG1 Ser326Cys多态性与肝细胞癌(HCC)易感性之间的任何关联。方法:在PubMed CNKI数据库中搜索所有可用文章。对应于95%置信区间(95%CI)的OR用来评估hOGG1 Ser326Cys多态性与HCC敏感性之间的关联。结果:七个病例对照研究,包括1,663例病例和1,675例对照,可用于该分析。在hOGG1 Ser326Cys多态性与HCC风险之间未发现关联(主要模型:OR = 0.695,95%CI:0.501-0.964,p = 0.029;加成模型:OR = 0.682,95%CI:0.374-1.245,p = 0.213;隐性模型:OR = 1.215,95%CI:0.711-2.078,p = 0.476)。敏感性分析不干扰结果。结论:这些发现表明hOGG1 Ser326Cys多态性可能在肝癌的发生中不起作用。但是,需要更大规模的研究来确认。

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