Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Faculty of Internal Medicine, School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Sci Rep. 2018 Oct 10;8(1):15058. doi: 10.1038/s41598-018-33448-1.
Hepatitis C virus (HCV) eradication by antivirals promote fibrosis modification. Whether host genetics determined fibrosis regression in chronic hepatitis C (CHC) patients with sustained virological response (SVR) is to be determined. One hundred and fifty-six SVR patients with paired liver biopsy before and after antivirals were enrolled. Host genetic factors including single nucleotide polymorphism rs17047200 of tolloid-like 1(TLL-1) were analyzed for their association with fibrosis modification. The proportions of improved, unchanged and worsening fibrotic stags were 39.1% (n = 61), 39.1% (n = 61), and 21.8% (n = 34), respectively. The rate of annual fibrotic improvement was 0.16 ± 0.79. There was a significant trend of increased fibrotic improvement rate in patients from F01 to F4 (P < 0.001). However, the rate of improvement seemed more limited in cirrhotic patients among those with advanced liver disease. Patients with fibrotic improvement had a significantly higher proportion of TLL-1 rs17047200 AA genotype compared to those without (92.5% vs. 79.3%, p = 0.039). Logistic regression analysis revealed that the TLL-1 rs17047200 AA genotype was the only independent factor associated with fibrosis improvement (odds ratio/95% confidence intervals: 3.2/1.01-10.12, p = 0.047). Compared with TLL-1 rs17047200 non-AA carriers, a significantly higher proportion of fibrosis improvement in AA genotype carriers was observed among patients with F0-2 (33.3% vs. 0%, p = 0.005) but not with F34 (70% vs. 80%, p = 1). We concluded that TLL-1 genetic variants determined fibrotic improvement in CHC with curative antivirals, particularly in patients with mild liver disease.
抗病毒治疗清除丙型肝炎病毒(HCV)可促进肝纤维化的改善。但尚不清楚宿主遗传学是否决定了慢性丙型肝炎(CHC)患者持续病毒学应答(SVR)后的纤维化消退。本研究纳入了 156 例抗病毒治疗前后有配对肝活检的 SVR 患者,分析了宿主遗传因素,包括 Toll 样 1(Toll-like 1,TLL-1)基因单核苷酸多态性 rs17047200,与纤维化改善的相关性。改善、不变和恶化纤维化阶段的比例分别为 39.1%(61 例)、39.1%(61 例)和 21.8%(34 例)。纤维化每年改善率为 0.16±0.79。纤维化改善率在 F01 至 F4 期患者中呈增加趋势(P<0.001)。然而,在晚期肝病患者中,肝硬化患者的改善率似乎更为有限。与无改善者相比,纤维化改善者 TLL-1 rs17047200 AA 基因型的比例明显更高(92.5%比 79.3%,P=0.039)。Logistic 回归分析显示,TLL-1 rs17047200 AA 基因型是与纤维化改善相关的唯一独立因素(比值比/95%置信区间:3.2/1.01-10.12,P=0.047)。与 TLL-1 rs17047200 非 AA 携带者相比,AA 基因型携带者在 F0-2 期患者中纤维化改善的比例明显更高(33.3%比 0%,P=0.005),而在 F34 期患者中无显著差异(70%比 80%,P=1)。综上所述,TLL-1 遗传变异决定了抗病毒治疗后 CHC 的纤维化改善,特别是在轻度肝病患者中。