Sun Qing, Guo Xuedan, Wang Qi, Zhao Fan
Department of Oncology, Wuxi 2nd People's Hospital, Affiliated to Nanjing Medical University, Wuxi 214002, China.
Chin J Cancer Res. 2016 Oct;28(5):536-542. doi: 10.21147/j.issn.1000-9604.2016.05.09.
Many studies have examined the association between the -308 G/A polymorphism gene polymorphisms and hepatocellular carcinoma risk in various populations, but their results have been inconsistent. To assess this relationship more precisely, a meta-analysis was performed.
The PubMed and CNKI (China National Knowledge Infrastructure) database was searched for case-control studies. Odds ratios (OR) with 95% CIs were used to determine the strength of association between the -308 G/A polymorphisms and HCC risk. The pooled ORs for the risk associated with the -308 G/A genotype, the A carriers (A/G + A/A) . the wild-type homozygotes (G/G), A/A . G/G were calculated, respectively. Subgroup analyses were done by ethnicity and smoking status. Heterogeneity assumptions were assessed by chi-square-based -test.
Ultimately, 21 studies, comprising 2,923 hepatocellular carcinoma cases and 4,323 controls were included. Overall, the A carriers (G/A + A/A) . the wild-type homozygotes (G/G), the pooled OR was 1.05 (95% CI, 0.93-1.19; P=0.000 for heterogeneity), for A/A . G/G the pooled OR was 1.07 (95% CI, 0.95-1.21; P=0.007 for heterogeneity). In the stratified analysis by ethnicity, the significantly risks were found among non-Asians. However, for Asians, significantly risks were not found.
The -308 G/A polymorphisms are not associated with hepatocellular carcinoma risk among Asians, but for non-Asians.
许多研究探讨了-308 G/A基因多态性与不同人群肝细胞癌风险之间的关联,但其结果并不一致。为了更精确地评估这种关系,进行了一项荟萃分析。
检索PubMed和中国知网(CNKI)数据库中的病例对照研究。采用比值比(OR)及95%置信区间(CI)来确定-308 G/A多态性与肝癌风险之间的关联强度。分别计算与-308 G/A基因型、A等位基因携带者(A/G + A/A)、野生型纯合子(G/G)、A/A与G/G相关风险的合并OR值。按种族和吸烟状况进行亚组分析。通过基于卡方的检验评估异质性假设。
最终纳入21项研究,包括2923例肝细胞癌病例和4323例对照。总体而言,A等位基因携带者(G/A + A/A)与野生型纯合子(G/G)相比,合并OR为1.05(95%CI,0.93 - 1.19;异质性P = 0.000);A/A与G/G相比,合并OR为1.07(95%CI,0.95 - 1.21;异质性P = 0.007)。在按种族进行的分层分析中,非亚洲人群中发现显著风险。然而,在亚洲人群中未发现显著风险。
-308 G/A多态性与亚洲人群的肝细胞癌风险无关,但与非亚洲人群有关。