HLA-DRB1等位基因多态性与肝癌发病风险关系的系统评价
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Association between HLA-DRB1 alleles polymorphism and hepatocellular carcinoma:a systematic review
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    目的:系统评价HLA-DRB1*07/12/15与肝癌[本文的肝癌指的是肝细胞癌(hepatocellular carcinoma,HCC)]的发病风险关系。方法:计算机检索PubMed、EMBASE、万方数据库、中国知网全文数据库(CNKI),纳入HLA-DRB1*07/12/15与HCC发病风险关系的病例对照研究,对纳入的研究提取有效数据,采用统计软件RevMan 5.0进行Meta分析,效应指标采用OR值表示。结果:HLA-DRB1*12/15增加了整个人群HCC的发病风险[(OR=1.56,95%CI=1.12~2.17,P=0.009)/(OR=1.35,95%CI=1.03~1.77,P=0.03)],HLA-DRB1*07与整个人群HCC的发病无明显关系(OR=0.99,95%CI=0.46~2.14,P=0.97);亚组分析结果提示:HLA-DRB1*12/15增加了亚洲人群HCC的发病风险[(OR=1.65,95%CI=1.17~2.32,P=0.004)/(OR=1.55,95%CI=1.14~2.11,P=0.006)],HLA-DRB1*07与亚洲人群HCC的发病风险无明显关系(OR=0.95,95%CI=0.26~3.50,P=0.94)。结论:HLA-DRB1*12/15增加了HCC的发病风险,HLA-DRB1*07与HCC的发病无明显关系。

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    Objective:To investigate the correlation between HLA-DRB1*07/12/15 and hepatocellular carcinoma(HCC). Methods:Articles were identified by electronic search in PubMed,EMBASE,Wanfang data,CNKI. Case-control study trials focusing on the correlation of the risk of HLA-DRB1*07/12/15 with HCC were included. Effective data were extracted from the eligible studies. All Meta analysis were performed by RevMan 5.0 software. ORs were used as effect indicators. Results:HLA-DRB1*12/15 increased the risk of HCC in the whole populations[(OR=1.56,95%CI=1.12 to 2.17,P=0.009)/(OR=1.35,95%CI=1.03 to 1.77,P=0.03)] while HLA-DRB1*07 didn’t correlated with the risk of HCC in the whole populations(OR=0.99,95%CI=0.46 to 2.14,P=0.97). Subgroup analyzis suggested that:HLA-DRB1*12/15 increased the risk of HCC in Asian populations[(OR=1.65,95%CI=1.17 to 2.32,P=0.004)/(OR=1.55,95%CI=1.14 to 2.11,P=0.006)],while HLA-DRB1*07 didn’t correlated with the risk of HCC in Asian populations significantly(OR=0.95,95%CI=0.26 to 3.50,P=0.94). Conclusion:HLA-DRB1*12/15 increases the risk of HCC while HLA-DRB1*07 doesn’t correlate with the risk of HCC.

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时志鹏,庄 汉,张大志,周 智,胡 鹏,任 红. HLA-DRB1等位基因多态性与肝癌发病风险关系的系统评价[J].重庆医科大学学报,2014,38(12):1727-1731

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  • 在线发布日期: 2015-11-06
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