Abstract

Treatment with indinavir (IDV), a protease inhibitor, is frequently associated with renal abnormalities. We determined the incidence of renal failure (creatinine clearance <80 mL min-1 1.73 (m(2))-1) in HIV patients treated with highly active antiretroviral therapy, including IDV, and investigated the possible mechanisms and risk factors of IDV nephrotoxicity. Thirty-six patients receiving IDV were followed for 3 years. All were assessed for age, body weight, duration of infection, duration of IDV treatment, sulfur-derivative use, total cholesterol, triglycerides, magnesium, sodium, potassium, creatinine, and urinalysis. We also determined renal function in terms of creatinine clearance, urine osmolality and fractional excretion of sodium, potassium, and water. Urinary nitrate (NO3) excretion was measured in 18 IDV-treated patients and compared with that of 8 patients treated with efavirenz, a drug without renal side effects. Sterile leukocyturia occurred in 80.5% of the IDV-treated patients. Creatinine clearance <80 mL min-1 1.73 (m(2))-1 was observed in 22 patients (61%) and was associated with low body weight and the use of sulfur-derivatives. These patients also had lower osmolality, lower urine volume and a higher fractional excretion of water compared to the normal renal function group. Urinary NO3 excretion was significantly lower in IDV-treated patients (809 +/- 181 microM NO3-/mg creatinine) than in efavirenz-treated patients (2247 +/- 648 microM NO3-/mg creatinine, P < 0.01). The lower NO3 excretion suggests that IDV decreases nitric oxide production.

Highlights

  • Since the introduction of HIV-1 protease inhibitors, the impact of antiretroviral therapy on the incidence of opportunistic infections has been thoroughly investigated and is well defined

  • We determined the incidence of renal failure (creatinine clearance

  • Indinavir is a potent protease inhibitor used for the treatment of individuals infected with HIV-1 and is a well-known cause of crystal-induced acute renal failure [16,17] and urinary complications

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Summary

Introduction

Since the introduction of HIV-1 protease inhibitors, the impact of antiretroviral therapy on the incidence of opportunistic infections has been thoroughly investigated and is well defined. The availability of highly active antiretroviral therapy (HAART) has resulted in profound and sustained reduction of HIV replication, improving CD4 cell counts, prolonging time to development of AIDS and improving AIDS survival rates [14]. Renal and urological complications are significant side effects of IDV use, and IDV has been implicated in the development of symptomatic crystalluria and nephrolithiasis in 3-50% of patients [6,7]. These complications have been associated with elevated plasma IDV concentrations [8]

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