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Effect of vitamin D supplementation on sustained virological response in genotype 1/4 chronic hepatitis C treatment-na?ve patients from India

机译:补充维生素D对印度基因型1/4慢性丙型肝炎初治患者持续病毒学应答的影响

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Background & objectives: The effect of vitamin D supplementation on response to antiviral therapy in hepatitis C virus (HCV) genotype 1 and 4 infection still remains unclear, with studies yielding inconsistent results. The aim of the present study was to assess the effect of vitamin D supplementation on treatment outcome in patients with genotype 1/4 chronic hepatitis C (CHC) infection. Methods: Sixty consecutive, treatment-na?ve, genotype 1 and 4 chronic HCV patients were included in the study. The patients were randomized into two groups: Vitamin D supplemented group received pegylated (PEG)-interferon α-2a 180 μg per week plus ribavirin (RBV) (1000-1200 mg/d) together with vitamin D3 (2000 IU/d) and control group received identical therapy without vitamin D (32 patients). Results: There were no significant differences between the two groups in terms of age, sex, body mass index and baseline laboratory values. Lower vitamin D levels were associated with higher grades of fibrosis in liver histology (vitamin D >20 ng/ml - 70% vs vitamin D PP=0.36), complete early viral response (53.2 vs 40%, P=0.34), end of treatment response (64 vs 46%, P=0.17) and sustained virological response (SVR) (60 vs 44%, P=0.19) as compared to control group. Interleukin 28B polymorphism [odds ratio (OR)-15.37, 95% confidence interval (CI)-2.32-101.76, P=0.04] and baseline serum vitamin D levels (OR-6.36, 95% CI-1.36-29.61 P=0.02) were independent predictors of SVR in genotype 1/4 CHC. Vitamin D supplementation was not found to be predictor of response in genotype 1/4 CHC on multivariate analysis (OR-2.79, 95% CI- 0.63-12.34, P=0.74). Interpretation & conclusions: The present study showed that addition of vitamin D to PEG/RBV combination therapy in treatment-na?ve patients who were infected with HCV genotype 1/4 had no effect on the rates of rapid, early and sustained viral responses.
机译:背景与目标:尚不清楚维生素D补充剂对丙型肝炎病毒(HCV)基因型1和4感染的抗病毒治疗反应的影响,研究结果不一致。本研究的目的是评估补充维生素D对基因型1/4慢性丙型肝炎(CHC)感染患者的治疗效果。方法:本研究包括连续60例初治的1型和4型慢性HCV患者。将患者随机分为两组:补充维生素D的组每周接受聚乙二醇化(PEG)-干扰素α-2a180μg加利巴韦林(RBV)(1000-1200 mg / d)以及维生素D3(2000 IU / d)和对照组接受无维生素D的相同疗法(32例)。结果:两组在年龄,性别,体重指数和基线实验室值方面均无显着差异。较低的维生素D水平与肝脏组织学中较高水平的纤维化有关(维生素D> 20 ng / ml-70%vs维生素D PP = 0.36),完全早期病毒应答(53.2 vs 40%,P = 0.34),与对照组相比,治疗反应(64 vs 46%,P = 0.17)和持续病毒学应答(SVR)(60 vs 44%,P = 0.19)。白介素28B多态性[比值比(OR)-15.37,95%置信区间(CI)-2.32-101.76,P = 0.04]和基线血清维生素D水平(OR-6.36,95%CI-1.36-29.61 P = 0.02)是1/4 CHC基因型SVR的独立预测因子。在多变量分析中,未发现补充维生素D是1/4 CHC基因型反应的预测因子(OR-2.79,95%CI-0.63-12.34,P = 0.74)。解释与结论:本研究表明,在初次感染HCV基因型1/4的初治患者中,在PEG / RBV联合治疗中添加维生素D对快速,早期和持续的病毒反应速率没有影响。

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