Journal Home
Search for

Volume 17, Issue 1, Pages 72-82 (January 2010)


View previous. 13 of 18 View next.

Antiretroviral Medications: Adverse Effects on the Kidney

Jennifer Jao, Christina M. WyattCorresponding Author Informationemail address

The widespread introduction of highly active antiretroviral therapy (HAART) in the mid-1990s dramatically altered the course of human immunodeficiency virus (HIV) infection, with improvements in survival and reductions in the incidence of AIDS-defining illnesses. Although antiretroviral therapy has been shown to reduce the incidence of both AIDS-defining and non-AIDS conditions, long-term exposure to HAART may also be associated with significant toxicity. This article reviews the potential nephrotoxicity of specific antiretroviral agents and the impact of antiretroviral therapy on related metabolic disorders. The antiretroviral agents most strongly associated with direct nephrotoxicity include the nucleotide reverse transcriptase inhibitor, tenofovir, and the protease inhibitor indinavir, although other agents have been implicated less frequently. Tenofovir and related nucleotide analogs have primarily been associated with proximal tubular dysfunction and acute kidney injury, whereas indinavir is known to cause nephrolithiasis, obstructive nephropathy, and interstitial nephritis. Kidney damage related to antiretroviral therapy is typically reversible with early recognition and timely discontinuation of the offending agent, and nephrologists should be familiar with the potential toxicity of these agents to avoid delays in diagnosis.

Divisions of Infectious Disease and Nephrology, Mount Sinai School of Medicine, New York, NY

Corresponding Author InformationAddress correspondence to Christina M. Wyatt, MD, Box 1243, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY 10029.

 Dr Wyatt has received research support from Gilead Sciences and from the Gilead Foundation.

PII: S1548-5595(09)00133-5

doi:10.1053/j.ackd.2009.07.009


View previous. 13 of 18 View next.