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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.
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页码:62 / 69
页数:8
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