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      Weight Gain Following Initiation of Antiretroviral Therapy: Risk Factors in Randomized Comparative Clinical Trials

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          Abstract

          Background

          Initiation of antiretroviral therapy (ART) often leads to weight gain. While some of this weight gain may be an appropriate return-to-health effect, excessive increases in weight may lead to obesity. We sought to explore factors associated with weight gain in several randomized comparative clinical trials of ART initiation.

          Methods

          We performed a pooled analysis of weight gain in 8 randomized controlled clinical trials of treatment-naive people living with human immunodeficiency virus (HIV) initiating ART between 2003 and 2015, comprising >5000 participants and 10 000 person-years of follow-up. We used multivariate modeling to explore relationships between demographic factors, HIV disease characteristics, and ART components and weight change following ART initiation.

          Results

          Weight gain was greater in more recent trials and with the use of newer ART regimens. Pooled analysis revealed baseline demographic factors associated with weight gain including lower CD4 cell count, higher HIV type 1 RNA, no injection drug use, female sex, and black race. Integrase strand transfer inhibitor use was associated with more weight gain than were protease inhibitors or nonnucleoside reverse transcriptase inhibitors (NNRTIs), with dolutegravir and bictegravir associated with more weight gain than elvitegravir/cobicistat. Among the NNRTIs, rilpivirine was associated with more weight gain than efavirenz. Among nucleoside/nucleotide reverse transcriptase inhibitors, tenofovir alafenamide was associated with more weight gain than tenofovir disoproxil fumarate, abacavir, or zidovudine.

          Conclusions

          Weight gain is ubiquitous in clinical trials of ART initiation and is multifactorial in nature, with demographic factors, HIV-related factors, and the composition of ART regimens as contributors. The mechanisms by which certain ART agents differentially contribute to weight gain are unknown.

          Abstract

          In this report, we use pooled data from randomized clinical trials to identify demographic-, human immunodeficiency virus-, and antiretroviral therapy (ART)–related risk factors for weight gain after the initiation of ART, highlighting the multifactorial nature of ART-associated weight gain.

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          Most cited references39

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          Dolutegravir plus Two Different Prodrugs of Tenofovir to Treat HIV

          Two drugs under consideration for inclusion in antiretroviral therapy (ART) regimens for human immunodeficiency virus (HIV) infection are dolutegravir (DTG) and tenofovir alafenamide fumarate (TAF). There are limited data on their use in low- and middle-income countries.
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            Obesity and the environment: where do we go from here?

            J O Hill (2003)
            The obesity epidemic shows no signs of abating. There is an urgent need to push back against the environmental forces that are producing gradual weight gain in the population. Using data from national surveys, we estimate that affecting energy balance by 100 kilocalories per day (by a combination of reductions in energy intake and increases in physical activity) could prevent weight gain in most of the population. This can be achieved by small changes in behavior, such as 15 minutes per day of walking or eating a few less bites at each meal. Having a specific behavioral target for the prevention of weight gain may be key to arresting the obesity epidemic.
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              Brief Report: Weight Gain in Persons With HIV Switched From Efavirenz-Based to Integrase Strand Transfer Inhibitor-Based Regimens.

              With the introduction of integrase strand transfer inhibitor (INSTI)-based antiretroviral therapy, persons living with HIV have a potent new treatment option. Recently, providers at our large treatment clinic noted weight gain in several patients who switched from efavirenz/tenofovir disoproxil fumarate/emtricitabine (EFV/TDF/FTC) to dolutegravir/abacavir/lamivudine (DTG/ABC/3TC). In this study, we evaluated weight change in patients with sustained virologic suppression who switched from EFV/TDF/FTC to an INSTI-containing regimen.
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                Author and article information

                Journal
                Clin Infect Dis
                Clin. Infect. Dis
                cid
                Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
                Oxford University Press (US )
                1058-4838
                1537-6591
                15 September 2020
                14 October 2019
                14 October 2019
                : 71
                : 6
                : 1379-1389
                Affiliations
                [1 ] Brigham and Women’s Hospital, Harvard Medical School , Boston, Massachusetts, USA
                [2 ] University of Colorado School of Medicine , Aurora, Colorado, USA
                [3 ] University of Texas Health Science Center , Houston, Texas, USA
                [4 ] University Hospitals Cleveland Medical Center and Case Western Reserve University , Cleveland, Ohio, USA
                [5 ] Barts Health National Health Service Trust , London, United Kingdom
                [6 ] University Hospital Essen , Essen, Germany
                [7 ] Johns Hopkins University School of Medicine , Baltimore, Maryland, USA
                [8 ] University Hospital Bonn , Bonn, Germany
                [9 ] Gilead Sciences, Inc , Foster City, California, USA
                [10 ] Infectious Disease Medical Center , Hamburg, Germany
                [11 ] King’s College Hospital National Health Service Foundation Trust , London, United Kingdom
                [12 ] Mortimer Market Center , London, United Kingdom
                [13 ] Vanderbilt University Medical Center , Nashville, Tennessee, USA
                Author notes
                Correspondence: M. Das, Gilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA 94494 ( moupali.das@ 123456gilead.com ).
                Author information
                http://orcid.org/0000-0001-7793-8011
                http://orcid.org/0000-0002-2844-1612
                Article
                ciz999
                10.1093/cid/ciz999
                7486849
                31606734
                e5665edf-9af0-4731-b744-b7c957caf206
                © The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 15 May 2019
                : 07 October 2019
                : 30 August 2019
                : 12 November 2019
                Page count
                Pages: 11
                Funding
                Funded by: Gilead Sciences, Inc;
                Categories
                Articles and Commentaries
                AcademicSubjects/MED00290

                Infectious disease & Microbiology
                hiv,weight gain,obesity,antiretroviral therapy,art
                Infectious disease & Microbiology
                hiv, weight gain, obesity, antiretroviral therapy, art

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