Title
Metabolic effects of preexposure prophylaxis with coformulated tenofovir disoproxil fumarate and emtricitabine
Date Issued
18 July 2018
Access level
open access
Resource Type
journal article
Author(s)
Glidden D.V.
Mulligan K.
McMahan V.
Anderson P.L.
Chariyalertsak S.
Buchbinder S.P.
Bekker L.G.
Schechter M.
Grinsztejn B.
Grant R.M.
Publisher(s)
Oxford University Press
Abstract
Background Antiretroviral drugs have been associated with changes in lipids, fat mass and dat distribution. Tenofovir disoproxil fumarate (TDF) has been shown to have a more favorable metabolic profile than other drugs in its class. However, the metabolic effects of TDF in preexposure prophylaxis (PrEP) are unknown. Methods We evaluated the effects of TDF/emtricitabine (FTC) on lipids and body composition in a blinded, placebo-controlled PrEP trial. Participants enrolled in a metabolic subcohort (N = 251, TDF/FTC; N = 247, placebo) consented to fasting lipid panels, dual-energy X-ray absorptiometry scans for body composition, and pharmacologic testing of drug metabolites at baseline and every 24 weeks thereafter. Results Lean body mass was stable and unaffected by TDF/FTC. Body weight increased in both groups but was lower on TDF/FTC through week 72. This difference was explained by lower fat accumulation on TDF/FTC. The net median percent difference (standard error, P value) for TDF/FTC vs placebo at week 24 was -0.8% (0.4%, P =.02),+0.3% (0.4%, P =.46), and -3.8% (1.4%, P =.009) for total, lean, and fat mass, respectively. There was no apparent differential regional fat accumulation on TDF/FTC. Decreases in cholesterol, but not triglycerides, were seen in TDF/FTC participants, with detectable drug levels compared to placebo. Conclusions TDF/FTC for PrEP showed cholesterol reductions and appeared to transiently suppress the accumulation of weight and body fat compared to placebo. There was no evidence of altered fat distribution or lipodystrophy during daily oral TDF/FTC PrEP.
Start page
411
End page
419
Volume
67
Issue
3
Language
English
OCDE Knowledge area
Ciencias socio biomédicas (planificación familiar, salud sexual, efectos políticos y sociales de la investigación biomédica) Enfermedades infecciosas
Scopus EID
2-s2.0-85048510668
PubMed ID
Source
Clinical Infectious Diseases
ISSN of the container
10584838
Sponsor(s)
Financial support. This work was supported by the NIAID (U01 AI106499, UM1 AI068619, U01 AI064002, R03 AI120819, R03 AI122908). Some infrastructure support at the University of California, San Francisco, was provided by an award from the NIH/National Academy for Advancing Translational Science (UL1 TR000004). The iPrEx studies were sponsored by the NIH with cofunding from the Bill and Melinda Gates Foundation. Gilead Sciences supported travel expenses for non-US investigators to attend study meetings. Potential conflicts of interest. R. M. G. has received fees from and a research grant from ViiV, a manufacturer of an investigational compound being investigated for use as PrEP. D. V. G. and M. S. have received fees from Gilead Sciences. P. L. A. has received a research grant from Gilead Sciences. All other authors: No reported conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
Sources of information: Directorio de Producción Científica Scopus