Shavakhi Ahmad, Minakari Mohamad, Bighamian Afshin, Sadeghian Sina, Shavakhi Sara, Khamisi Naser, Khodadustan Mahsa, Talebi Majid, Ataei Behrooz
Department of Gastroenterology and Hepatology, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Gastroenterology and Hepatology, Shahrekord University of Medical Sciences, Isfahan, Iran.
J Res Med Sci. 2014 Mar;19(Suppl 1):S1-4.
Lipid metabolism is one of the hepatitis C virus (HCV) life cycle steps. Statins can reduce cholesterol level and finally can decrease HCV replication. Thus, we assessed the effect of Statins in combination with standard antiviral treatment on hyperlipidemic genotype I HCV infected patients.
This study was a prospective clinical trial. 40 patients were selected from those referred to educational and Therapeutic Centers of Isfahan University of Medical Sciences from 2009 to 2010 with confirmed HCV viremia. All patients received Peg-interferon-a2a and ribavirin. 20 hyperlipidemic Patients received 20 mg atorvastatin nightly for 3 months and placebo was prescribed for 20 normolipidemic HCV infected patients as a control group. Liver enzymes and complete blood count were checked monthly and thyroid stimulating hormone was checked every 3 months. We also performed quantitative HCV-ribonucleic acid (RNA) test in 12(th) week of therapy, at the end of treatment and 6 months after therapy for all samples.
We didn't find any significant differences in the mean of HCV-RNA numbers between statin and placebo groups in 12(th) week of treatment, in the end of treatment and 6 months after treatment (P > 0.05).
Atorvastatin has no effect on the mean of HCV viral load when we added it to standard treatment for hepatitis C infection. Further studies are necessary to examine the possible antiviral properties of statins and their potential role as adjuncts to standard HCV therapy.
脂质代谢是丙型肝炎病毒(HCV)生命周期的步骤之一。他汀类药物可降低胆固醇水平,最终可减少HCV复制。因此,我们评估了他汀类药物与标准抗病毒治疗联合应用对高脂血症I型HCV感染患者的影响。
本研究为前瞻性临床试验。从2009年至2010年转诊至伊斯法罕医科大学教育与治疗中心且确诊为HCV病毒血症的患者中选取40例。所有患者均接受聚乙二醇干扰素α-2a和利巴韦林治疗。20例高脂血症患者每晚服用20mg阿托伐他汀,持续3个月,20例血脂正常的HCV感染患者服用安慰剂作为对照组。每月检查肝酶和全血细胞计数,每3个月检查促甲状腺激素。我们还对所有样本在治疗第12周、治疗结束时和治疗后6个月进行了HCV核糖核酸(RNA)定量检测。
在治疗第12周、治疗结束时和治疗后6个月,他汀类药物组和安慰剂组的HCV-RNA数量平均值之间未发现任何显著差异(P>0.05)。
将阿托伐他汀添加到丙型肝炎感染的标准治疗中时,其对HCV病毒载量平均值没有影响。有必要进行进一步研究以检验他汀类药物可能的抗病毒特性及其作为标准HCV治疗辅助药物的潜在作用。