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Review
. 2024 Oct 15;79(4):999-1005.
doi: 10.1093/cid/ciae191.

Antiretrovirals and Weight Change: Weighing the Evidence

Affiliations
Review

Antiretrovirals and Weight Change: Weighing the Evidence

David Alain Wohl et al. Clin Infect Dis. .

Abstract

Body weight is influenced by an interplay of individual and environmental factors. In people with human immunodeficiency virus (HIV), weight is also influenced by disease status with loss accompanying disease progression that is reversed with effective antiretroviral therapy. Weight changes in comparative antiretroviral therapy trials differ by regimen, with greater gains observed with the integrase strand transfer inhibitors dolutegravir and bictegravir, particularly when coadministered with tenofovir alafenamide fumarate, compared with regimens that include agents such as tenofovir disoproxil fumarate that attenuate weight gain. We review weight changes in major randomized trials of preexposure prophylaxis and initial and switch HIV therapy, highlighting the challenges to assessing the role of antiretroviral therapy in weight change. This examination forms the basis for a model that questions assumptions regarding an association between integrase strand transfer inhibitors and tenofovir alafenamide fumarate and excessive weight gain and calls for more careful consideration of these data when making HIV treatment decisions.

Keywords: antiretroviral therapy (ART); clinical trials; preexposure prophylaxis (PrEP); weight change; weight gain.

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Conflict of interest statement

Potential conflicts of interest . D. A. W. has received honoraria for consultancy from Gilead Sciences, ViiV Healthcare, Janssen Pharmaceuticals, Merck & Co, Theratechnologies, and EMD Serono. His institution has received grant funding to support his research from Gilead Sciences, ViiV Healthcare, and Merck & Co. J. R. K. has served as a consultant to Gilead, Merck, Theratechnologies, and Janssen Pharmaceuticals and has received research support from Gilead Sciences and Merck. P. E. S. has served as a scientific advisory board member/consultant for Gilead Sciences, GlaxoSmithKline/ViiV Healthcare, Merck & Co, and Janssen Pharmaceuticals, He has received research support from Gilead Sciences, and GlaxoSmithKline/ViiV Healthcare. G. A. M. has received consultant fees from Janssen Pharmaceuticals, Gilead Sciences, ViiV Healthcare, Merck, and Theratechnologies. D. R. K. is a consultant to and received honoraria from AbbVie, Gilead Sciences, GlaxoSmithKline, Janssen, Pharmaceuticals, Merck & Co, Roche, and ViiV Healthcare. He has received research support from Gilead Sciences, ViiV Healthcare, Merck & Co, and Roche and has provided expert testimony on behalf of Gilead Sciences and Janssen. G. M. has served as an advisor to Novartis and Ipsen Pharmaceuticals and a speaker for Gilead Sciences, GlaxoSmithKline, Merck Sharp & Dohme UK, and ViiV Healthcare. L. K. is a scientific and/or medical consultant to Altimmune, Boehringer Ingelheim, Gilead Sciences, Glyscend, Intellihealth, Johnson & Johnson, Eli Lilly, Novo Nordisk, Pfizer, Sidekick Health, twenty30.health, and Xeno Biosciences. J. v. W. is employed by ViiV Healthcare. R. E. C. is employed by Merck & Co. C. C. is employed by Gilead Sciences. 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.

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