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综述文章:慢性丙型肝炎基因型 4、5 和 6 的流行病学和治疗。

Review article: the epidemiology and therapy of chronic hepatitis C genotypes 4, 5 and 6.

机构信息

Department of Medicine, Stanford University Medical Center, Palo Alto, CA, USA.

出版信息

Aliment Pharmacol Ther. 2014 Jan;39(2):137-47. doi: 10.1111/apt.12551. Epub 2013 Nov 19.

Abstract

BACKGROUND

The global burden of hepatitis C (HCV) infection is mostly found in Africa, the Middle East and Asia, where HCV genotypes 4, 5 and 6 are common. The literature on these genotypes is sparse and this synopsis will review characteristics of patients infected with these genotypes.

AIM

To review characteristics of patients infected with HCV genotypes 4, 5 and 6.

METHODS

PubMed search for 'hepatitis C' AND 'genotype 4', 'hepatitis C' AND 'genotype 5', and 'hepatitis C' AND 'genotype 6' was conducted and relevant articles were reviewed.

RESULTS

Intravenous drug use is generally responsible for HCV genotype 4 infection in developed countries, but unsafe medical practices cause most cases of HCV genotypes 4, 5 and 6 in endemic countries. The sustained virological response (SVR) rate for patients with HCV genotype 4 who receive pegylated interferon and ribavirin for 48 weeks ranges from 40% to 70% in various small studies. The SVR rate is in the 60-70% range for HCV genotype 5 and 70-80% range for HCV genotype 6 following 48 weeks with pegylated interferon and ribavirin. Preliminary data suggest that a shorter course of 24 weeks of pegylated interferon and ribavirin may be acceptable for HCV genotype 6, with an SVR rate of approximately 70%.

CONCLUSIONS

The current standard-of-care therapy for HCV genotypes 4, 5 and 6 is pegylated interferon and ribavirin for 48 weeks. A shorter course with 24 weeks of therapy may be considered for patients with genotype 6. Newer and much more effective therapies may be forthcoming in the next few years.

摘要

背景

丙型肝炎(HCV)感染的全球负担主要发生在非洲、中东和亚洲,这些地区常见 HCV 基因型 4、5 和 6。关于这些基因型的文献很少,这篇综述将回顾感染这些基因型的患者的特征。

目的

综述感染 HCV 基因型 4、5 和 6 的患者的特征。

方法

在 PubMed 上进行了“hepatitis C”和“genotype 4”、“hepatitis C”和“genotype 5”以及“hepatitis C”和“genotype 6”的搜索,并对相关文章进行了回顾。

结果

在发达国家,静脉吸毒通常是 HCV 基因型 4 感染的原因,但在流行地区,不安全的医疗实践导致大多数 HCV 基因型 4、5 和 6 感染病例。在各种小型研究中,接受聚乙二醇干扰素和利巴韦林治疗 48 周的 HCV 基因型 4 患者的持续病毒学应答(SVR)率在 40%-70%之间。接受聚乙二醇干扰素和利巴韦林治疗 48 周后,HCV 基因型 5 的 SVR 率在 60%-70%之间,HCV 基因型 6 的 SVR 率在 70%-80%之间。初步数据表明,接受聚乙二醇干扰素和利巴韦林治疗 24 周的疗程可能更短,对于 HCV 基因型 6,SVR 率约为 70%。

结论

目前,HCV 基因型 4、5 和 6 的标准治疗方法是聚乙二醇干扰素和利巴韦林治疗 48 周。对于基因型 6 的患者,可以考虑更短的 24 周疗程。在未来几年内,可能会出现更新、更有效的治疗方法。

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