Impact of Tenofovir on Renal Function in HIV-Infected, Antiretroviral-Naive Patients

被引:108
|
作者
Horberg, Michael [1 ,2 ]
Tang, Beth [3 ]
Towner, William [4 ]
Silverberg, Michael [2 ]
Bersoff-Matcha, Susan [5 ]
Hurley, Leo [2 ]
Chang, Joseph [4 ]
Blank, Jackie [5 ]
Quesenberry, Charles, Jr. [2 ]
Klein, Daniel [6 ]
机构
[1] Kaiser Permanente, HIV AIDS, HIV Initiat, Oakland, CA 94612 USA
[2] Kaiser Permanente No Calif, Div Res, Oakland, CA USA
[3] Kaiser Permanente So Calif, Res & Evaluat, Pasadena, CA USA
[4] Kaiser Permanente, HIV Med, Los Angeles, CA USA
[5] Kaiser Permanente, Dept Infect Dis, Rockville, MD USA
[6] Kaiser Permanente, HIV Infect Dis, Hayward, CA USA
关键词
tenofovir; renal function; proximal tubular dysfunction; antiretroviral therapy; CHRONIC KIDNEY-DISEASE; DISOPROXIL FUMARATE; FANCONI-SYNDROME; TUBULAR DYSFUNCTION; SERUM CREATININE; THERAPY; FAILURE; SAFETY; REGIMENS; EPIDEMIOLOGY;
D O I
10.1097/QAI.0b013e3181be6be2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To better characterize the long-term effects of tenofovir on renal function in a large managed care organization. Methods: We performed a retrospective cohort analysis in Kaiser Permanente for years 2002 to 2005 comparing renal function among antiretroviral naive patients initiating a tenofovir-containing regimen (964 patients) or tenofovir-sparing regimens (683 patients). We evaluated glomerular filtration rate (GFR, (Modification of Diet in Renal Disease equation]), serum creatinine, and the development of renal proximal tubular dysfunction. We report multivariable hazard ratios (HR, Cox modeling) and linear outcomes (repeated measures) with predictors retained if P < 0.10 (backward selection). Potential predictor variables included in multivariate models were age, sex, Black race, baseline laboratories (including CD4 count), history of diabetes mellitus, hypertension, malignancy, hepatitis, and concurrent medications. Results: Overall, tenofovir-exposed patients had a larger relative decline in GFR through 104 weeks (-7.6 mL/min/1.73 m(2) relative to tenofovir-sparing, P < 0.001.); the degree of the difference varied by baseline GFR, with the greatest effect seen in those patients with GFR greater than 80 mL/min/1.73 m(2). Tenofovir-exposed patients had greater development of proximal tubular dysfunction over time (at 52 wk: HRadjusted = 1.95 [P = 0.01] and at 104 wk: HRadjusted = 5.23 [P = 0.0004]) and had greater risk of medication discontinuation (HRadjusted = 1.21, P = 0.02), especially as renal function worsened. Viral control and CD4 count changes were similar between the two groups. Conclusions: Tenofovir is associated with greater effect on decline in renal function and a higher risk of proximal tubular dysfunction in antiretroviral naive patients initiating antiretroviral therapy.
引用
收藏
页码:62 / 69
页数:8
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