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Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population

机译:中国人群干扰素γ多态性与乙肝病毒相关的肝硬化风险

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Previous studies proved that interferon gamma (IFN-γ) gene polymorphisms were associated with the risk of hepatitis B virus (HBV) infection. However, the association between IFN-γ polymorphisms and HBV-related liver cirrhosis (HBV-LC) risk is still unclear. IFN-γ +874 T/A and +2109G/A genotypes were determined in 126 HBV-LC patients, 129 chronic hepatitis B(CHB) patients, and 173 early HBV infection controls using a sequence-specific primer-polymerase chain reaction and a polymerase chain reaction-restriction fragment length polymorphism, respectively. Significant associations were observed between +2109A/G polymorphisms and HBV-LC risk in the co-dominant model (GG vs. AA: OR = 0.321, 95% CI = 0.130-0.793, P = 0.014), the allelic model (OR = 0.565, 95% CI = 0.388-0.825, P = 0.003), the dominant model (OR = 0.551, 95% CI = 0.344-0.883, P = 0.013), and the recessive model (OR = 0.385, 95% CI = 0.159-0.930, P = 0.034). In addition, haplotype analysis indicated that the T+874G+2109 haplotype significantly decreased the HBV-LC risk (OR = 0.106, 95% CI = 0.022-0.502, P = 0.000), and A+874A+2109 haplotype significantly increased the LC risk (OR = 1.485, 95% CI = 1.065-2.070, P = 0.019). No significant associations were observed between IFN-γ +874 T/A polymorphisms and HBV-LC risk, as well as the two single-nucleotide polymorphisms (SNPs) and CHB risk (P  0.05). Our observations suggested a significant association of IFN-γ polymorphisms with HBV-LC risk in the Chinese population.
机译:先前的研究证明干扰素γ(IFN-γ)基因多态性与乙型肝炎病毒(HBV)感染的风险有关。但是,IFN-γ多态性与HBV相关肝硬化(HBV-LC)风险之间的关联仍不清楚。使用序列特异性引物-聚合酶链反应和PCR检测了126名HBV-LC患者,129名慢性乙型肝炎(CHB)患者和173名早期HBV感染对照中的IFN-γ+874 T / A和+ 2109G / A基因型。聚合酶链反应-限制性片段长度多态性。在等位基因模型(共显性模型)中,在共显性模型中(+ 2109A / G多态性与HBV-LC风险之间存在显着关联)(GG与AA:OR = 0.321,95%CI = 0.130-0.793,P = 0.014)。 0.565,95%CI = 0.388-0.825,P = 0.003),显性模型(OR = 0.551,95%CI = 0.344-0.883,P = 0.013),隐性模型(OR = 0.385,95%CI = 0.159) -0.930,P = 0.034)。另外,单倍型分析表明,T + 874G + 2109单倍型显着降低了HBV-LC风险(OR = 0.106,95%CI = 0.022-0.502,P = 0.000),而A + 874A + 2109单倍体则显着提高了LC风险(OR = 1.485,95%CI = 1.065-2.070,P = 0.019)。 IFN-γ+874 T / A多态性与HBV-LC风险以及两个单核苷酸多态性(SNPs)和CHB风险之间没有显着相关性(P> 0.05)。我们的观察结果表明,中国人群中IFN-γ多态性与HBV-LC风险显着相关。

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