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首页> 外文期刊>Antiviral therapy >Low-dose pegylated interferon-α2a plus ribavirin therapy for elderly and/or cirrhotic patients with HCV genotype-1b and high viral load
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Low-dose pegylated interferon-α2a plus ribavirin therapy for elderly and/or cirrhotic patients with HCV genotype-1b and high viral load

机译:低剂量聚乙二醇化干扰素-α2a联合利巴韦林治疗HCV基因型1b和高病毒载量的老年和/或肝硬化患者

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摘要

Background: Pegylated interferon (PEG-IFN) plus ribavirin therapy is still recommended for elderly and/or cirrhotic patients. This study examined whether sustained virological response (SVR) to low-dose PEG-IFN-α2a plus ribavirin therapy for elderly and/or cirrhotic patients could be predicted based on viral reduction within 2 weeks after therapy initiation or interleukin IL-(28B) polymorphism and viral mutations. Methods: Participants comprised 115 elderly (≥65 years) and/or cirrhotic patients with genotype-1b and high viral load. Reduced doses of PEG-IFN-α2a (90 μg/kg/week) and ribavirin (400-800 mg/day) were administered for 48-72 weeks based on virological response of each patient. Results: SVR was achieved in 34% (39/115), and treatment was discontinued in 15% (17/115). Univariate analysis identified age, α-fetoprotein, fibrosis marker, interferon sensitivity-determining region (ISDR), IL-28B polymorphism and level of viral reduction within 2 weeks as factors contributing significantly to SVR. However, no significant differences were noted in core amino acid substitutions. Multivariate analysis identified age, hyaluronic acid, ISDR and viral reduction as factors independently associated with SVR. Positive predictive value (PPV) and negative predictive value (NPV) of SVR based on the level of viral reduction at 2 weeks (cutoff level, 1.7 log IU/ml) were 83% and 84%, respectively. The PPV of SVR based on IL-28B major and ISDR mutant was 70%, and the NPV of SVR based on IL-28B minor and wild-type ISDR was 89%. Conclusions: Evaluations of viral reduction at 2 weeks or both IL-28B and ISDR are useful to predict SVR to low-dose PEG-IFN-α2a plus ribavirin therapy for elderly and/or cirrhotic patients.
机译:背景:对于老年人和/或肝硬化患者,仍建议使用聚乙二醇化干扰素(PEG-IFN)联合利巴韦林治疗。这项研究检查了是否可以根据治疗开始后2周内的病毒减少或白介素IL-(28B)多态性来预测对老年和/或肝硬化患者低剂量PEG-IFN-α2a加利巴韦林治疗的持续病毒学应答(SVR)和病毒突变。方法:参与者包括115名基因型1b和高病毒载量的老年人(≥65岁)和/或肝硬化患者。根据每位患者的病毒学应答,将降低剂量的PEG-IFN-α2a(90μg/ kg /周)和利巴韦林(400-800 mg /天)给药48-72周。结果:SVR达到34%(39/115),而中止治疗的比例为15%(17/115)。单因素分析确定了年龄,α-甲胎蛋白,纤维化标志物,干扰素敏感性决定区(ISDR),IL-28B多态性和2周内病毒减少水平是显着影响SVR的因素。但是,在核心氨基酸取代中没有发现显着差异。多变量分析确定年龄,透明质酸,ISDR和病毒减少是与SVR独立相关的因素。基于2周时病毒减少水平(临界水平,1.7 log IU / ml),SVR的阳性预测值(PPV)和阴性预测值(NPV)分别为83%和84%。基于IL-28B大分子和ISDR突变体的SVR的PPV为70%,基于IL-28B小分子和野生型ISDR的SVR的NPV为89%。结论:评估2周时的病毒减少或IL-28B和ISDR两者均有助于预测SVR对老年和/或肝硬化患者的小剂量PEG-IFN-α2a加利巴韦林治疗。

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