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丙型肝炎病毒与直接作用抗病毒药物(DAAs)时代的血脂。

Hepatitis C virus and lipids in the era of direct acting antivirals (DAAs).

机构信息

Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.

出版信息

Clin Res Hepatol Gastroenterol. 2013 Feb;37(1):10-6. doi: 10.1016/j.clinre.2012.07.002. Epub 2012 Sep 5.

Abstract

The six different HCV-genotypes have marked differences in response to therapy with pegylated interferon-α and ribavirin. The introduction of the direct acting antiviral (DAA) protease inhibitors, telaprevir and boceprevir in combination with pegylated interferon-α and ribavirin has become the new standard of care for genotype 1 infection. Several host factors associated with response to pegylated interferon-α and ribavirin are not as important in predicting response to triple therapy, and yet low-density lipoprotein cholesterol (LDLC) and statin use remain important associations of outcome with DAAs. This review focuses on the clinical associations between lipids and treatment response to interferon based antiviral treatments. We consider how understanding the interactions of HCV and host lipid metabolism remains relevant in the era of DAAs for genotype 1 infection and for treatment of non-genotype 1 chronic hepatitis C.

摘要

六种不同的 HCV 基因型在聚乙二醇干扰素-α和利巴韦林治疗中的反应有明显差异。直接作用抗病毒(DAA)蛋白酶抑制剂替拉瑞韦和博赛泼维与聚乙二醇干扰素-α和利巴韦林联合应用已成为治疗 1 型感染的新标准。一些与聚乙二醇干扰素-α和利巴韦林治疗反应相关的宿主因素在预测三联疗法反应中并不那么重要,但低密度脂蛋白胆固醇(LDLC)和他汀类药物的使用仍然与 DAA 的治疗结果有重要关联。本综述重点关注基于干扰素的抗病毒治疗与血脂之间的临床关联。我们考虑了在 DAA 治疗 1 型感染和非 1 型慢性丙型肝炎的时代,了解 HCV 和宿主脂质代谢相互作用仍然具有相关性。

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