Wei Fangfang, Zheng Qiaolan, Li Maoyin, Wu Maosheng
Department of Infectious Disease, Guangdong Second Provincial General Hospital Journal Center Department of Urology, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong Province, China.
Medicine (Baltimore). 2017 May;96(19):e6835. doi: 10.1097/MD.0000000000006835.
More and more studies focus on the relationship between hepatitis B virus (HBV) basal core promoter/precore (BCP/PC) mutations, but it remains controvercial, we conducted a meta-analysis to investigate the features of hepatitis B virus basal core promoter/precore mutations on the progression of hepatocellular carcinoma (HCC).
A comprehensive search was conducted for articles published between January 1, 2005 and December 31, 2015 using the following databases: PubMed, Embase, Cochrane Library, Wanfang, and China National Knowledge Infrastructure. Medical subject heading terms were prioritized in setting the search strategy. Search terms included ("hepatitis B virus"), ("mutation or mutations or mutant"), and ("hepatocellular carcinoma" or "liver cancer" or hepatoma). A meta-analysis of pooled results from case-control studies examined the association between mutations G1896A, A1762T, G1764A, and A1762T/G1764A and the risk of HCC.
We included 29 articles for analysis and found that G1896A (summary odds ratios [OR] = 2.04, 95% confidence interval [CI] = 1.41-2.95), A1762T (summary OR = 3.96, 95% CI = 1.98-7.92), G1764A (summary OR = 3.48, 95% CI = 1.99-6.09), and A1762T/G1764A (summary OR = 3.96, 95% CI = 2.77-5.65) are each associated with a statistically significant increase in the risk of HCC.
In summary, we found that G1896A, A1762T, G1764A, and A1762T/G1764A are associated with an increased risk of HCC.
越来越多的研究聚焦于乙型肝炎病毒(HBV)基础核心启动子/前核心(BCP/PC)突变之间的关系,但仍存在争议。我们进行了一项荟萃分析,以研究乙型肝炎病毒基础核心启动子/前核心突变在肝细胞癌(HCC)进展中的特征。
使用以下数据库对2005年1月1日至2015年12月31日发表的文章进行全面检索:PubMed、Embase、Cochrane图书馆、万方和中国知网。在制定检索策略时优先使用医学主题词。检索词包括(“乙型肝炎病毒”)、(“突变或多种突变或突变体”)以及(“肝细胞癌”或“肝癌”或“肝细胞瘤”)。对病例对照研究的汇总结果进行荟萃分析,以检验G1896A、A1762T、G1764A和A1762T/G1764A突变与HCC风险之间的关联。
我们纳入了29篇文章进行分析,发现G1896A(汇总比值比[OR]=2.04,95%置信区间[CI]=1.41 - 2.95)、A1762T(汇总OR=3.96,95% CI=1.98 - 7.92)、G1764A(汇总OR=3.48,95% CI=1.99 - 6.09)和A1762T/G1764A(汇总OR=3.96,95% CI=2.77 - 5.65)均与HCC风险的统计学显著增加相关。
总之,我们发现G1896A、A1762T、G1764A和A1762T/G1764A与HCC风险增加相关。