Aleagha Omid Emami, Oltulu Pembe, Sadeghi Masoud
Molecular Pathology Research Center, Imam Reza Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Clinical Research Development Center, Imam Reza Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Clin Exp Hepatol. 2020 Dec;6(4):359-366. doi: 10.5114/ceh.2020.102171. Epub 2020 Dec 30.
We reported the association between interleukin 6 polymorphisms (rs1800796, rs1800795, rs2069837, rs17147230, and rs1800797) and hepatocellular carcinoma (HCC) susceptibility in a meta-analysis.
The studies were retrieved by searching the search terms in Scopus, PubMed, Web of Science, and Cochrane Library databases until June 2020. The analyses were done by RevMan 5.3 software using odds ratios (ORs) and 95% confidence intervals (CIs) and the analysis of publication bias and sensitivity analyses were performed by CMA 2.0 software.
Searching through the databases, 316 records were retrieved and finally 13 studies were analyzed in the present meta-analysis. For the rs1800797 polymorphism, there was an elevated risk of AA genotype (OR = 2.68, = 0.03) in HCC patients compared to healthy controls. Also, there was an elevated risk of AA (OR = 3.06, = 0.04) and GA (OR = 2.61, = 0.005) genotypes in HCC patients compared to liver cirrhosis patients. For rs2069837 polymorphism, there was an elevated risk of GG genotype (OR = 2.25, = 0.01) in HCC patients compared to healthy controls. For rs17147230, T allele (OR = 1.31, = 0.03) and TT genotype (OR = 1.83, = 0.02) had elevated risks in HCC patients compared to healthy controls.
The present meta-analysis confirmed that there was an elevated risk of the AA and GA genotypes of rs1800797 polymorphism and the GG genotype of rs2069837, and the T allele and TT genotype of rs17147230 in HCC.
我们在一项荟萃分析中报告了白细胞介素6基因多态性(rs1800796、rs1800795、rs2069837、rs17147230和rs1800797)与肝细胞癌(HCC)易感性之间的关联。
通过在Scopus、PubMed、Web of Science和Cochrane图书馆数据库中检索检索词来获取研究,检索截至2020年6月。使用RevMan 5.3软件通过比值比(OR)和95%置信区间(CI)进行分析,并使用CMA 2.0软件进行发表偏倚分析和敏感性分析。
通过数据库检索,共检索到316条记录,最终在本荟萃分析中分析了13项研究。对于rs1800797基因多态性,与健康对照相比,HCC患者中AA基因型的风险升高(OR = 2.68,P = 0.03)。此外,与肝硬化患者相比,HCC患者中AA(OR = 3.06,P = 0.04)和GA(OR = 2.61,P = 0.005)基因型的风险升高。对于rs2069837基因多态性,与健康对照相比,HCC患者中GG基因型的风险升高(OR = 2.25,P = 0.01)。对于rs17147230,与健康对照相比,HCC患者中T等位基因(OR = 1.31,P = 0.03)和TT基因型(OR = 1.83,P = 0.02)的风险升高。
本荟萃分析证实,rs1800797基因多态性的AA和GA基因型、rs2069837的GG基因型以及rs17147230的T等位基因和TT基因型在HCC中的风险升高。