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Safety and efficacy of sofosbuvir-containing regimens in hepatitis C-infected patients with impaired renal function.含索磷布韦方案在肾功能受损的丙型肝炎感染患者中的安全性和有效性。
Liver Int. 2016 Jun;36(6):807-16. doi: 10.1111/liv.13102. Epub 2016 Mar 24.
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Sofosbuvir and Simeprevir for the Treatment of Recurrent Hepatitis C with Fibrosing Cholestatic Hepatitis after Liver Transplantation.索磷布韦和西米普明治疗肝移植后复发性丙型肝炎伴纤维化胆汁淤积性肝炎
Int J Organ Transplant Med. 2016;7(1):38-45. Epub 2016 Feb 1.
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Successful Treatment of Hepatitis C in Renal Transplant Recipients With Direct-Acting Antiviral Agents.直接作用抗病毒药物治疗肾移植受者丙型肝炎的疗效。
Am J Transplant. 2016 May;16(5):1588-95. doi: 10.1111/ajt.13620. Epub 2016 Feb 5.
4
Chronic kidney disease: Treatment of hepatitis C virus infection in patients with CKD.慢性肾脏病:慢性肾脏病患者丙型肝炎病毒感染的治疗
Nat Rev Nephrol. 2016 Jan;12(1):5-6. doi: 10.1038/nrneph.2015.189. Epub 2015 Nov 23.
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Efficacy and Safety of Sofosbuvir-Based Antiviral Therapy to Treat Hepatitis C Virus Infection After Kidney Transplantation.索磷布韦为基础的抗病毒治疗在肾移植后治疗丙型肝炎病毒感染的疗效和安全性。
Am J Transplant. 2016 May;16(5):1474-9. doi: 10.1111/ajt.13518. Epub 2015 Nov 20.
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Sofosbuvir and Velpatasvir for HCV Genotype 2 and 3 Infection.索磷布韦和维帕他韦治疗 2 型和 3 型丙型肝炎病毒感染。
N Engl J Med. 2015 Dec 31;373(27):2608-17. doi: 10.1056/NEJMoa1512612. Epub 2015 Nov 17.
7
Sofosbuvir and Velpatasvir for HCV Genotype 1, 2, 4, 5, and 6 Infection.索磷布韦和维帕他韦治疗 1、2、4、5、6 型 HCV 感染。
N Engl J Med. 2015 Dec 31;373(27):2599-607. doi: 10.1056/NEJMoa1512610. Epub 2015 Nov 16.
8
Pharmaceutical management of hepatitis B and C in liver and kidney transplant recipients.肝肾移植受者的乙型和丙型肝炎药物治疗
World J Gastrointest Pharmacol Ther. 2015 Nov 6;6(4):105-10. doi: 10.4292/wjgpt.v6.i4.105.
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A review of direct-acting antivirals for the treatment of hepatitis C in patients with advanced chronic kidney disease.用于治疗晚期慢性肾病患者丙型肝炎的直接抗病毒药物综述。
Nephrol Dial Transplant. 2017 Jan 1;32(1):35-41. doi: 10.1093/ndt/gfv361.
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Grazoprevir plus elbasvir in treatment-naive and treatment-experienced patients with hepatitis C virus genotype 1 infection and stage 4-5 chronic kidney disease (the C-SURFER study): a combination phase 3 study.格拉瑞韦联合艾尔巴韦在初治和经治的丙型肝炎病毒基因型 1 感染和 4-5 期慢性肾脏病患者中的疗效(C-SURFER 研究):一项联合 III 期研究。
Lancet. 2015 Oct 17;386(10003):1537-45. doi: 10.1016/S0140-6736(15)00349-9. Epub 2015 Oct 5.

慢性肾脏病中的丙型肝炎病毒感染

Hepatitis C Virus Infection in Chronic Kidney Disease.

作者信息

Ladino Marco, Pedraza Fernando, Roth David

机构信息

Division of Nephrology and Hypertension, University of Miami Miller School of Medicine and the Miami Veterans Administration Hospital, Miami, Florida.

Division of Nephrology and Hypertension, University of Miami Miller School of Medicine and the Miami Veterans Administration Hospital, Miami, Florida

出版信息

J Am Soc Nephrol. 2016 Aug;27(8):2238-46. doi: 10.1681/ASN.2016010030. Epub 2016 Apr 19.

DOI:10.1681/ASN.2016010030
PMID:27095799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4978066/
Abstract

Soon after the hepatitis C virus (HCV) was identified in 1989, it was recognized that the prevalence of infection in patients with ESRD far exceeded that in the general population. Infection with HCV predisposes to the hepatic complications of cirrhosis and hepatocellular carcinoma. However, important extrahepatic manifestations include immune complex glomerular disease, accelerated progression of CKD, increases in cardiovascular event risk, and lymphoproliferative disorders. Advances in understanding the molecular biology of HCV have ushered in a new era in the treatment of this infection. Second generation direct-acting antiviral agents have revolutionized therapy, with sustained virologic response rates (undetectable viral load 12 weeks after completing therapy) of >90% in most patients. Studies using direct-acting antivirals in patients with CKD and those on dialysis are showing excellent safety and efficacy as well. In this context, it is imperative that nephrologists become familiar with this literature, reviewed here, so that the important decisions, including which patients should be treated and the optimal timing to initiate therapy, are vetted in association with the compounding issues of CKD, ESRD, and kidney transplantation.

摘要

1989年丙型肝炎病毒(HCV)被发现后不久,人们就认识到终末期肾病(ESRD)患者中的感染率远远超过普通人群。HCV感染易引发肝硬化和肝细胞癌等肝脏并发症。然而,重要的肝外表现包括免疫复合物性肾小球疾病、慢性肾脏病(CKD)进展加速、心血管事件风险增加以及淋巴增殖性疾病。对HCV分子生物学认识的进展开启了这种感染治疗的新时代。第二代直接作用抗病毒药物彻底改变了治疗方式,大多数患者的持续病毒学应答率(完成治疗12周后病毒载量不可检测)超过90%。在CKD患者和透析患者中使用直接作用抗病毒药物的研究也显示出极佳的安全性和疗效。在此背景下,肾脏病学家必须熟悉本文所综述的这些文献,以便在考虑CKD、ESRD和肾移植等复杂问题的情况下,对包括哪些患者应接受治疗以及开始治疗的最佳时机等重要决策进行审查。