Neutrophil gelatinase-associated lipocalin, a marker of tubular dysfunction, is not increased in long-term virologically controlled patients receiving a tenofovir/emtricitabine + nevirapine regimen

Details

Serval ID
serval:BIB_AEFB9AEE2739
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Neutrophil gelatinase-associated lipocalin, a marker of tubular dysfunction, is not increased in long-term virologically controlled patients receiving a tenofovir/emtricitabine + nevirapine regimen
Journal
J Antimicrob Chemother
Author(s)
Allavena C., Bach-Ngohou K., Billaud E., Secher S., Dejoie T., Reliquet V., Fakhouri F., Raffi F.
ISSN
1460-2091 (Electronic)
ISSN-L
0305-7453
Publication state
Published
Issued date
12/2013
Volume
68
Number
12
Pages
2866-70
Language
english
Notes
Allavena, C
Bach-Ngohou, K
Billaud, E
Secher, S
Dejoie, T
Reliquet, V
Fakhouri, F
Raffi, F
eng
Research Support, Non-U.S. Gov't
England
J Antimicrob Chemother. 2013 Dec;68(12):2866-70. doi: 10.1093/jac/dkt265. Epub 2013 Jun 30.
Abstract
OBJECTIVES: Tenofovir may be associated with nephrotoxicity. Several studies have shown that an early increase in urinary neutrophil gelatinase-associated lipocalin (NGAL) may predict the occurrence of acute kidney injury. We investigated urine and plasma NGAL in patients on long-term treatment with nevirapine associated with either tenofovir/emtricitabine or abacavir/lamivudine. PATIENTS AND METHODS: We studied 40 virologically controlled Caucasian patients on stable treatment (median >4 years) with tenofovir/emtricitabine + nevirapine (n = 20) or abacavir/lamivudine + nevirapine (n = 20), and no history of kidney disease, high blood pressure or diabetes. Plasma immunovirological parameters (NGAL and C-reactive protein) and urinary NGAL, beta2-microglobulin and alpha1-microglobulin were measured during a routine clinical visit. RESULTS: Median concentrations of NGAL were in the normal range, but were significantly higher in the abacavir/lamivudine group compared with the tenofovir/emtricitabine group both in the plasma, at 74.9 and 66.0 ng/mL (P = 0.032), respectively, and in the urine, at 36.1 and 12.8 ng/mL (P = 0.017), respectively. CONCLUSIONS: Plasma and urinary NGAL concentrations remained in the normal range in this long-term virologically controlld population without any overt renal disease. The usefulness of NGAL in detecting sub-clinical renal dysfunction appears to be very limited.
Keywords
Acute-Phase Proteins/*urine, Adenine/adverse effects/*analogs & derivatives/therapeutic use, Adult, Anti-HIV Agents/adverse effects/*therapeutic use, Cross-Sectional Studies, Deoxycytidine/adverse effects/*analogs & derivatives/therapeutic use, Emtricitabine, Female, HIV Infections/*drug therapy, Humans, Lipocalin-2, Lipocalins/*blood/*urine, Male, Middle Aged, Nevirapine/adverse effects/*therapeutic use, Organophosphonates/adverse effects/*therapeutic use, Proto-Oncogene Proteins/*blood/*urine, Tenofovir, HIV infection, Ngal, nucleoside analogues, renal toxicity
Pubmed
Create date
01/03/2022 10:18
Last modification date
02/03/2022 6:36
Usage data