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Body Composition Changes After Initiation of Raltegravir or Protease Inhibitors: ACTG A5260s.
- Source :
-
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America [Clin Infect Dis] 2016 Apr 01; Vol. 62 (7), pp. 853-62. Date of Electronic Publication: 2016 Jan 20. - Publication Year :
- 2016
-
Abstract
- Background: Fat gain after antiretroviral therapy (ART) occurs, and its association with protease inhibitors (PIs) is unclear.<br />Methods: Peripheral and central fat depots and lean mass were measured using standardized and centrally read abdominal CT scans and whole-body dual-energy absorptiometry scans over a 96-week period in human immunodeficiency virus (HIV)-infected treatment-naive participants. The patients were randomized to tenofovir-emtricitabine (TDF/FTC) plus atazanavir-ritonavir (ATV/r), darunavir-ritonavir (DRV/r), or raltegravir (RAL) in ACTG A5260s, a substudy of A5257. Within arm changes were assessed with signed-rank tests. The 96-week percentage changes in fat and lean mass in the 2 PI arms were not different, thus the PI arms were combined and compared to the RAL arm. Associations between baseline biomarkers and changes in body composition were assessed. All analyses used linear regression models.<br />Results: 328 patients were randomized (90% male, 44% white non-Hispanic). The median age was 36 years, HIV-1 RNA 4.6 log10 copies/mL, and CD4 349 cells/μL. Overall, at week 96, increases in limb fat (13.4%), subcutaneous (19.9%) and visceral abdominal fat (25.8%), trunk fat (18%), and lean mass (1.8%) were apparent (P < .001 for changes within each arm). Changes for all fat and lean outcomes were not different between the PI arms or between the RAL and the combined PI arms. Higher baseline HIV-1 RNA levels were associated with greater gains in peripheral and central fat.<br />Conclusions: In treatment-naive participants initiating ART with TDF/FTC, no differences in lean mass and regional fat were found with RAL when compared with ATV/r or DRV/r over 96 weeks.<br />Clinical Trials Registration: NCT00811954 and NCT00851799.<br /> (© The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail journals.permissions@oup.com.)
- Subjects :
- Adult
Anti-HIV Agents therapeutic use
Female
HIV Infections virology
Humans
Male
Middle Aged
Protease Inhibitors adverse effects
Protease Inhibitors therapeutic use
RNA, Viral blood
Raltegravir Potassium therapeutic use
Viral Load drug effects
Weight Gain drug effects
Abdominal Fat drug effects
Anti-HIV Agents adverse effects
Body Composition drug effects
HIV Infections drug therapy
Raltegravir Potassium adverse effects
Subjects
Details
- Language :
- English
- ISSN :
- 1537-6591
- Volume :
- 62
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
- Publication Type :
- Academic Journal
- Accession number :
- 26797215
- Full Text :
- https://doi.org/10.1093/cid/ciw017