Department of Gastroenterology and Hepatology, Kinki University School of Medicine, Osaka-Sayama, Japan.
Digestion. 2011;84 Suppl 1:56-61. doi: 10.1159/000333215. Epub 2011 Dec 2.
Pegylated interferon (PEG-IFN) plus ribavirin therapy is the current standard treatment for chronic hepatitis C (CHC) genotype 1 with high viral load. A common genetic variation near the IL28B gene has been found to affect the response to PEG-IFN plus ribavirin therapy for CHC. The aims of this study were to analyze the association between the rs8099917 genotype and treatment response in a cohort study of CHC.
This study evaluated clinical and laboratory parameters retrospectively in a cohort of 122 patients with chronic hepatitis C with genotype 1 and a high viral load who received PEG-IFN plus ribavirin therapy. We carried out univariate and multivariate statistical analyses of parameters and clinical responses.
Sixty-three of 122 patients (51.6%) had sustained virological responses (SVRs). Patients with the rs8099917 genotype TT achieved significantly higher SVR rates (p < 0.01). Univariate analysis revealed that SVRs were associated with BMI, fibrosis, albumin, total cholesterol, PEG-IFN dose, ribavirin dose and the rs8099917 genotype. Multivariate analysis revealed that the rs8099917 genotype (odds ratio 7.434, 95% CI 2.278-24.257, p = 0.001) and total PEG-IFN dose (odds ratio 7.162, 95% CI 1.565-18.15, p = 0.007) were significant factors.
The rs8099917 genotype and total PEG-IFN dose were associated with SVR in patients with hepatitis C virus genotype 1.
聚乙二醇干扰素(PEG-IFN)联合利巴韦林治疗是目前高病毒载量慢性丙型肝炎(CHC)基因型 1 的标准治疗方法。在 IL28B 基因附近发现了一种常见的遗传变异,它会影响 CHC 患者对 PEG-IFN 联合利巴韦林治疗的反应。本研究旨在对慢性丙型肝炎患者队列研究中 IL28B 基因附近的 rs8099917 基因型与治疗反应的相关性进行分析。
本研究回顾性评估了 122 例基因型 1 高病毒载量慢性丙型肝炎患者接受 PEG-IFN 联合利巴韦林治疗的临床和实验室参数。我们对参数和临床反应进行了单变量和多变量统计分析。
122 例患者中 63 例(51.6%)获得持续病毒学应答(SVR)。rs8099917 基因型 TT 的患者获得了更高的 SVR 率(p<0.01)。单变量分析显示,SVR 与 BMI、纤维化、白蛋白、总胆固醇、PEG-IFN 剂量、利巴韦林剂量和 rs8099917 基因型有关。多变量分析显示,rs8099917 基因型(比值比 7.434,95%可信区间 2.278-24.257,p=0.001)和总 PEG-IFN 剂量(比值比 7.162,95%可信区间 1.565-18.15,p=0.007)是显著因素。
rs8099917 基因型和总 PEG-IFN 剂量与丙型肝炎病毒基因型 1 患者的 SVR 相关。