Department of Infection and Liver Diseases, Liver Research Center, First Affiliated Hospital of Wenzhou Medical College, No. 2 Fuxue Lane, Wenzhou, Zhejiang, China.
Int J Infect Dis. 2010 Jul;14(7):e580-5. doi: 10.1016/j.ijid.2009.08.010. Epub 2009 Dec 9.
Previous studies on the tumor necrosis factor-alpha (TNF-alpha)-308 gene promoter polymorphism in chronic hepatitis B virus (HBV) infection have reported conflicting results.
We carried out a meta-analysis of 21 studies in relation to the TNF-alpha-308 gene promoter, involving a total of 4230 chronic HBV infection cases and 2905 controls.
The overall meta-analysis indicated that -308A heterozygotes (GA) had a significant 27% decreased risk of developing chronic hepatitis B (CHB) (odds ratio (OR) 0.73; 95% confidence interval (CI) 0.57-0.93; p=0.012). For -308A allele homozygotes (AA) and carriers (GA+AA), the pooled odd ratios both indicated a significantly decreased risk of CHB (OR 0.28; 95% CI 0.19-0.43; p=0.0001; and OR 0.70; 95% CI 0.55-0.89; p=0.004, respectively). In subgroup analyses by ethnicity, a significantly decreased risk was associated with -308 variant genotypes (GA and AA) in Mongoloid populations in all genetic models. However, no significant associations were found in Caucasoids. Moreover, in the subgroup analyses by control group, significantly decreased risk was associated with -308 variant genotypes (GA and AA) in the group of spontaneously recovered cases in all genetic models; however, no significant associations were found in the group of healthy cases.
The TNF-alpha-308A allele is a protective factor for chronic HBV infection, especially in Mongoloids.
先前关于肿瘤坏死因子-α(TNF-α)-308 基因启动子多态性与慢性乙型肝炎病毒(HBV)感染的研究结果相互矛盾。
我们对 21 项 TNF-α-308 基因启动子相关研究进行了荟萃分析,共纳入 4230 例慢性 HBV 感染病例和 2905 例对照。
总体荟萃分析表明,-308A 杂合子(GA)发生慢性乙型肝炎(CHB)的风险显著降低 27%(优势比(OR)0.73;95%置信区间(CI)0.57-0.93;p=0.012)。对于-308A 等位基因纯合子(AA)和携带者(GA+AA),合并的 OR 均表明 CHB 的风险显著降低(OR 0.28;95% CI 0.19-0.43;p=0.0001;OR 0.70;95% CI 0.55-0.89;p=0.004)。按种族亚组分析,在所有遗传模型中,蒙古人种的-308 变异基因型(GA 和 AA)均与 CHB 风险显著降低相关。然而,在白种人群中未发现显著相关性。此外,按对照组亚组分析,在所有遗传模型中,自发恢复病例组的-308 变异基因型(GA 和 AA)与 CHB 风险显著降低相关;然而,在健康对照组中未发现显著相关性。
TNF-α-308A 等位基因是慢性 HBV 感染的保护因素,尤其是在蒙古人种中。