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Quantitative assessment of HLA-DQ gene polymorphisms with the development of hepatitis B virus infection clearance liver cirrhosis and hepatocellular carcinoma

机译:HLA-DQ基因多态性随乙型肝炎病毒感染清除肝硬化和肝细胞癌发展的定量评估

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摘要

Hepatitis B is one of the most common infectious diseases, which leads to public health problems in the world, especially in Asian counties. In recent years, extensive human genetic association studies have been carried out to identify susceptible genes and genetic polymorphisms to understand the genetic contributions to the disease progression of HBV infection. HLA-DQ gene variations have been reported to be associated with HBV infection/clearance, disease progression and the development of hepatitis B-related complications, including liver cirrhosis (LC) and hepatocellular carcinoma (HCC). However, the results are either inconclusive or controversial. Therefore, to derive a more precise estimation of the association, a meta-analysis was performed. Our data revealed that the HLA-DQ alleles rs2856718-G, rs7453920-A and rs9275319-G were significantly associated with decreased risk of HBV infection and HBV natural clearance. Logistic regression analyses showed that HLA-DQ alleles rs9275572-A significantly increased HBV infection clearance, and decreased HBV natural clearance. However, rs2856718-G and rs9275572-A were not associated with development of cirrhosis. The HLA-DQ polymorphisms (rs2856718 and rs9275572) were associated with a decreased HBV-related HCC risk in all genetic models, but rs9272105-A increased the risk of HBV-related HCC. In addition, no significant association was observed between HLA-DQ rs9275319-G polymorphism and HBV-related HCC. These stratified analyses were limited due to relatively modest size of correlational studies. In future, further investigation on a large population and different ethnicities are warranted. Our findings contribute to the personalized care and prognosis in hepatitis B.
机译:乙型肝炎是最常见的传染病之一,导致世界范围内的公共卫生问题,尤其是在亚洲县。近年来,已经进行了广泛的人类遗传协会研究,以鉴定易感基因和遗传多态性,以了解遗传因素对HBV感染疾病进展的影响。据报道,HLA-DQ基因变异与HBV感染/清除,疾病进展以及与乙型肝炎相关的并发症(包括肝硬化(LC)和肝细胞癌(HCC))的发展有关。但是,结果要么是不确定的,要么是有争议的。因此,为了获得对关联的更精确的估计,进行了荟萃分析。我们的数据显示,HLA-DQ等位基因rs2856718-G,rs7453920-A和rs9275319-G与降低HBV感染风险和HBV自然清除率显着相关。 Logistic回归分析显示,HLA-DQ等位基因rs9275572-A显着增加了HBV感染清除率,并降低了HBV自然清除率。但是,rs2856718-G和rs9275572-A与肝硬化的发展无关。在所有遗传模型中,HLA-DQ多态性(rs2856718和rs9275572)与HBV相关的HCC风险降低相关,但rs9272105-A增加了HBV相关的HCC风险。此外,未观察到HLA-DQ rs9275319-G多态性与HBV相关HCC之间的显着关联。由于相关研究规模相对较小,这些分层分析受到了限制。将来,有必要对大量人口和不同种族进行进一步调查。我们的发现有助于乙型肝炎的个性化护理和预后。

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