Weight Change Following Antiretroviral Therapy Switch in People With Viral Suppression: Pooled Data from Randomized Clinical Trials

Author:

Erlandson Kristine M1,Carter Christoph C2,Melbourne Kathleen2,Brown Todd T3,Cohen Cal2,Das Moupali2,Esser Stefan4,Huang Hailin2,Koethe John R5,Martin Hal2,McComsey Grace A67,Orkin Chloe8,Post Frank A9,Rockstroh Jürgen K10,Sax Paul E11,Stellbrink Hans-Jürgen12,Waters Laura13,Wei Xuelian2,Lake Jordan E14

Affiliation:

1. Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA

2. Gilead Sciences, Inc, Foster City, California, USA

3. Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA

4. Department of Dermatology, University Hospital Essen, Essen, Germany

5. Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA

6. University Hospitals Health System, Cleveland, Ohio, USA

7. Department of Medicine and Pediatrics, Case Western Reserve University, Cleveland, Ohio, USA

8. Barts Health National Health Service Trust, London, United Kingdom

9. King’s College Hospital National Health Service Foundation Trust, London, United Kingdom

10. Department of Medicine, University Hospital Bonn, Bonn, Germany

11. Department of Medicine, Brigham and Women’s Hospital and Harvard Medicine School, Boston, Massachusetts, USA

12. ICH Study Center, Hamburg, Germany

13. Mortimer Market Center, London, United Kingdom

14. Department of Medicine, University of Texas Health Science Center, Houston, Texas, USA

Abstract

Abstract Background We sought to identify factors associated with weight gain in randomized clinical trials of antiretroviral therapy (ART) switch. Methods We explored the effects of demographic factors, clinical characteristics, and ART on weight gain in a pooled analysis of 12 prospective clinical trials, wherein virologically suppressed people living with human immunodeficiency virus (PWH) were randomized to switch or remain on a stable baseline regimen (SBR). Results Both PWH randomized to switch ART (n = 4166) and those remaining on SBR (n = 3150) gained weight. Median weight gain was greater in those who switched (1.6 kg, interquartile range [IQR], –.05 to 4.0 vs 0.4 kg, [IQR], –1.8 to 2.4 at 48 weeks, P < .0001), with most weight gain occurring in the first 24 weeks after switch. Among baseline demographic and clinical characteristics, only younger age and lower baseline body mass index were associated with any or ≥10% weight gain. By week 48, 4.6% gained ≥10% weight (6.4% of switch and 2.2% of SBR), the greatest risk was with switch from efavirenz (EFV) to rilpivirine (RPV) or elvitegravir/cobicistat and switch from tenofovir disoproxil fumarate (TDF) to tenofovir alafenamide (TAF). Switch from abacavir to TAF was associated with less weight gain than switch from TDF to TAF and was not associated with increased risk for ≥10% weight gain. Conclusions Moderate weight gain after ART switch was common and usually plateaued by 48 weeks. Baseline ART was a predictor of post-switch weight gain; participants who switched off of EFV and TDF had the greatest weight gain. The biological mechanisms that underlie the differential effects of switching ART agents on weight and associated clinical implications require further study.

Funder

Gilead Sciences, Inc

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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