Tenofovir-Associated Kidney Toxicity in HIV-Infected Patients: A Review of the Evidence

被引:283
|
作者
Hall, Andrew M. [1 ]
Hendry, Bruce M. [2 ]
Nitsch, Dorothea [3 ]
Connolly, John O. [1 ]
机构
[1] UCL, UCL Ctr Nephrol, London NW3 2PF, England
[2] Kings Coll London, Dept Renal Med, London WC2R 2LS, England
[3] London Sch Hyg & Trop Med, Fac Epidemiol & Populat Hlth, London WC1, England
关键词
Kidney; Fanconi syndrome; Tenofovir; toxicity; REVERSE-TRANSCRIPTASE INHIBITORS; ACQUIRED-IMMUNODEFICIENCY-SYNDROME; NEPHROGENIC DIABETES-INSIPIDUS; ACTIVE ANTIRETROVIRAL THERAPY; FANCONI-SYNDROME; DISOPROXIL FUMARATE; RENAL-FAILURE; MITOCHONDRIAL TOXICITY; TUBULAR DYSFUNCTION; ANTIVIRAL DRUGS;
D O I
10.1053/j.ajkd.2011.01.022
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Tenofovir (TDF) is an effective and widely used treatment for both human immunodeficiency virus (HIV) and hepatitis B virus infection. Although studies suggest that TDF has a low overall toxicity profile and only a modest effect on estimated glomerular filtration rate, numerous case reports have since appeared in the literature describing TDF-associated renal tubular dysfunction, and this is now a significant source of HIV-related referrals to nephrologists. The main target of toxicity appears to be the proximal tubule, and in severe cases, patients can develop renal Fanconi syndrome. We review findings from recent studies in this area performed by ourselves and others and discuss our direct experience as practicing nephrologists. In particular, we discuss: (1) the nature and extent of TDF-associated kidney toxicity in the HIV-infected population, (2) potential underlying mechanisms of toxicity in the proximal tubule, (3) risk factors for developing tubular dysfunction, and (4) suggested strategies to monitor patients on TDF therapy. Am J Kidney Dis. 57(5): 773-780. (C) 2011 by the National Kidney Foundation, Inc.
引用
收藏
页码:773 / 780
页数:8
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