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Association Between Catalase Gene Polymorphisms and Risk of Chronic Hepatitis B Hepatitis B Virus-Related Liver Cirrhosis and Hepatocellular Carcinoma in Guangxi Population

机译:过氧化氢酶基因多态性与广西人群慢性乙型肝炎乙型肝炎病毒相关性肝硬化和肝细胞癌风险之间的关系

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摘要

Reactive oxygen species (ROS) play critical roles in hepatocarcinogenesis. The catalase (CAT) enzyme is involved in the repair of ROS. Therefore, we investigate the association between CAT gene polymorphisms and the risk of hepatocellular carcinoma (HCC).A total of 715 subjects were divided into 4 groups: 111 chronic hepatitis B (CHB) patients, 90 hepatitis B virus (HBV)-related liver cirrhosis (LC) patients, 266 HBV-HCC patients, and 248 healthy controls. The polymerase chain reaction-restriction fragment length polymorphism strategy was used to detect CAT gene rs1001179, rs769217, and rs7943316 polymorphisms.Binary logistic regression analyses adjusting for sex, age, ethnicity, smoking and alcohol consumption, and body mass index suggested that subjects carrying the rs769217 T allele were at marginally increased risk of CHB, LC, and HCC, with adjusted odds ratios (ORs) of 1.51 (95% confidence interval [CI] = 1.04–2.20, P = 0.029), 1.48 (95% CI = 1.03–2.14, P = 0.035), and 1.51 (95% CI = 1.14–1.98, P = 0.004), respectively. Similarly, those individuals carrying the rs769217 TT genotype had a moderately increased risk of CHB, LC, and HCC, with adjusted ORs of 2.11 (95% CI = 1.05–4.22, P = 0.035), 2.00 (95% CI, 1.01–3.95, P = 0.047), and 1.93 (95% CI = 1.14–3.28, P = 0.015), respectively. Moreover, subjects carrying the rs769217 CT genotype and at least 1 copy of the T allele (dominant model) were 1.78 times and 1.83 times more likely to develop HCC, respectively (OR = 1.78, 95% CI = 1.16–2.73, P = 0.009 and OR = 1.83, 95% CI = 1.23–2.71, P = 0.003). This association between CAT rs769217 T alleles and HCC risk is significantly strengthened among men, nonsmokers, nondrinkers, and among individuals <50 years of age. Furthermore, we found 1 high-risk haplotype GTA for CHB (OR = 1.45, 95% CI = 1.05–2.01) and 1 protective haplotype GCA for HCC risk (OR = 0.67, 95% CI = 0.52–0.87). We did not found any significant difference in CAT rs1001179 and rs7943316 polymorphisms between controls and cases.Our findings suggest that the CAT rs769217 T allele is associated with increased risk of CHB, HBV-LC, and HBV-HCC in Guangxi population.
机译:活性氧(ROS)在肝癌发生中起关键作用。过氧化氢酶(CAT)酶参与ROS的修复。因此,我们调查了CAT基因多态性与肝细胞癌(HCC)风险之间的关系。总共715名受试者分为4组:111例慢性乙型肝炎(CHB)患者,90例乙型肝炎病毒(HBV)相关肝肝硬化(LC)患者,266例HBV-HCC患者和248名健康对照者。聚合酶链反应-限制性片段长度多态性策略用于检测CAT基因rs1001179,rs769217和rs7943316多态性。通过对性别,年龄,种族,吸烟和饮酒和身体质量指数进行调整的二元logistic回归分析表明,携带rs769217 T等位基因患CHB,LC和HCC的风险略有增加,调整后的优势比(OR)为1.51(95%置信区间[CI] = 1.04–2.20,P = 0.029),1.48(95%CI = 1.03分别为–2.14,P = 0.035)和1.51(95%CI = 1.14–1.98,P = 0.004)。同样,携带rs769217 TT基因型的个体患CHB,LC和HCC的风险适度增加,调整后的OR为2.11(95%CI%= 1.05–4.22,P = 0.035),2.00(95%CI,1.01-3.95) ,P = 0.047)和1.93(95%CI = 1.14-3.28,P = 0.015)。此外,携带rs769217 CT基因型和至少1个T等位基因(优势模型)的受试者发生肝癌的可能性分别为1.78倍和1.83倍(OR = 1.78,95%CI = 1.16-2.73,P = 0.009和OR = 1.83,95%CI = 1.23-2.71,P = 0.003)。 CAT rs769217 T等位基因与HCC风险之间的这种关联在男性,非吸烟者,非饮酒者以及年龄小于50岁的人群中显着增强。此外,我们发现CHB有1个高风险单倍型GTA(OR = 1.45,95%CI = 1.05-2.01)和1个保护性单倍型GCA伴有HCC风险(OR = 0.67,95%CI = 0.52-0.87)。我们在对照组和病例之间未发现CAT rs1001179和rs7943316多态性的显着差异。我们的发现表明CAT rs769217 T等位基因与广西人群CHB,HBV-LC和HBV-HCC的风险增加有关。

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