Department of Gastroenterology, Ajou University School of Medicine, Suwon, Republic of Korea.
J Med Virol. 2013 May;85(5):808-14. doi: 10.1002/jmv.23551.
Polymorphisms in the primary microRNA region may be associated with natural course of hepatitis B virus (HBV) infection. This study evaluated if the mircoRNA 219-1 (miR-219-1) polymorphism can influence the susceptibility towards persistence of HBV infection and the progression to hepatocellular carcinoma (HCC) in patients with chronic HBV infection. A total of 1,439 individuals having either past or present evidence of HBV infection were enrolled for the study. The subjects were divided into four groups; (1) spontaneous recovery (n = 404), (2) chronic HBV carrier (n = 313), (3) chronic HBV carrier with cirrhosis (n = 305), and (4) hepatocellular carcinoma (n = 417). Genotyping was performed at three polymorphic variants (rs421446, rs107822, and rs213210) in the pri-miRNA region of miR-219-1. The rs421446 T allele was found to be strongly associated with HBV clearance (OR = 0.73, P = 0.0005 in a codominant model and OR = 0.67, P = 0.0009 in a dominant model, OR = 0.69, P = 0.04 in a recessive model, respectively). The rs107822 G allele was also found to be associated with HBV clearance (OR = 0.79, P = 0.008 in a codominant model and OR = 0.72, P = 0.01 in a dominant model, respectively). In haplotype analysis, ht2 (T-G-T) and ht1 (C-A-C) were found to be in significant association with the clearance of HBV. However, no significant association was observed between miR-219-1 polymorphism and the risk of HCC occurrence. This result suggests that polymorphisms in the pri-miRNA region of miR-219-1 might be a genetic factor for HBV clearance after infection.
miR-219-1 基因多态性与乙型肝炎病毒感染自然史的关系
miR-219-1 基因多态性与乙型肝炎病毒(HBV)感染的自然史有关。本研究评估了微小 RNA 219-1(miR-219-1)多态性是否会影响慢性 HBV 感染者对 HBV 感染持续存在的易感性以及向肝细胞癌(HCC)的进展。共有 1439 名既往或目前有 HBV 感染证据的个体被纳入本研究。将受试者分为四组:(1)自发恢复组(n=404);(2)慢性 HBV 携带者组(n=313);(3)慢性 HBV 携带者伴肝硬化组(n=305);(4)肝细胞癌组(n=417)。对 miR-219-1 前 miRNA 区三个多态性变异体(rs421446、rs107822 和 rs213210)进行基因分型。rs421446T 等位基因与 HBV 清除呈强相关(在共显性模型中 OR=0.73,P=0.0005;在显性模型中 OR=0.67,P=0.0009;在隐性模型中 OR=0.69,P=0.04)。rs107822G 等位基因也与 HBV 清除相关(在共显性模型中 OR=0.79,P=0.008;在显性模型中 OR=0.72,P=0.01)。在单体型分析中,ht2(T-G-T)和 ht1(C-A-C)与 HBV 清除呈显著相关。然而,miR-219-1 多态性与 HCC 发生风险之间未观察到显著相关性。该结果表明,miR-219-1 前 miRNA 区的多态性可能是感染后 HBV 清除的遗传因素。