Weight Gain Among Treatment-Naïve Persons With HIV Receiving Dolutegravir in Kenya.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
15 12 2022
Historique:
received: 24 05 2022
accepted: 16 08 2022
pmc-release: 15 12 2023
pubmed: 21 9 2022
medline: 15 11 2022
entrez: 20 9 2022
Statut: ppublish

Résumé

Several recent studies have linked integrase strand transfer inhibitors (INSTI) with increased weight gain. The effects of sex on weight gain with dolutegravir (DTG)-based antiretroviral therapy (ART) among treatment-naïve participants in a lower-income, sub-Saharan population with high rates of pre-ART underweight and tuberculosis (TB) coinfection are unknown. Our analysis included treatment-naïve participants in Kenya and starting their first treatment regimen between January 1, 2015, and September 30, 2018. Participants were grouped into 2 cohorts based on the initial treatment regimen [DTG vs. nonnucleoside reverse transcriptase inhibitors (NNRTI)]. We modelled weight changes over time using a multivariable nonlinear mixed-effect model, with participant as a random effect. Logistic regression models were constructed to evaluate the association between different variables with extreme increase in body mass index (≥10% increase). Seventeen thousand forty-four participants met our inclusion criteria. Sixty-two percent of participants were women, 6% were receiving active TB therapy, and 97% were on NNRTI-based regimens. Participants starting DTG-based regimens were more likely to gain weight when compared with participants starting NNRTI-based regimens. Female participants starting DTG-based regimens experienced the highest weight gain compared with other participants (mean gain of 6.1 kgs at 18 months). Female participants receiving DTG-based regimens, along with participants with lower CD4 cell counts, underweight at baseline, and those receiving active TB therapy were also at higher risk for extreme body mass index increase. Our study in a lower-income sub-Saharan African population confirms higher weight gain with DTG-based regimens compared with traditional ART for treatment-naïve patients.

Sections du résumé

BACKGROUND
Several recent studies have linked integrase strand transfer inhibitors (INSTI) with increased weight gain.
SETTING
The effects of sex on weight gain with dolutegravir (DTG)-based antiretroviral therapy (ART) among treatment-naïve participants in a lower-income, sub-Saharan population with high rates of pre-ART underweight and tuberculosis (TB) coinfection are unknown.
METHODS
Our analysis included treatment-naïve participants in Kenya and starting their first treatment regimen between January 1, 2015, and September 30, 2018. Participants were grouped into 2 cohorts based on the initial treatment regimen [DTG vs. nonnucleoside reverse transcriptase inhibitors (NNRTI)]. We modelled weight changes over time using a multivariable nonlinear mixed-effect model, with participant as a random effect. Logistic regression models were constructed to evaluate the association between different variables with extreme increase in body mass index (≥10% increase).
RESULTS
Seventeen thousand forty-four participants met our inclusion criteria. Sixty-two percent of participants were women, 6% were receiving active TB therapy, and 97% were on NNRTI-based regimens. Participants starting DTG-based regimens were more likely to gain weight when compared with participants starting NNRTI-based regimens. Female participants starting DTG-based regimens experienced the highest weight gain compared with other participants (mean gain of 6.1 kgs at 18 months). Female participants receiving DTG-based regimens, along with participants with lower CD4 cell counts, underweight at baseline, and those receiving active TB therapy were also at higher risk for extreme body mass index increase.
CONCLUSIONS
Our study in a lower-income sub-Saharan African population confirms higher weight gain with DTG-based regimens compared with traditional ART for treatment-naïve patients.

Identifiants

pubmed: 36126175
doi: 10.1097/QAI.0000000000003087
pii: 00126334-202212150-00011
pmc: PMC9814314
mid: NIHMS1834152
doi:

Substances chimiques

dolutegravir DKO1W9H7M1
Heterocyclic Compounds, 3-Ring 0
Oxazines 0
Pyridones 0
Reverse Transcriptase Inhibitors 0
HIV Integrase Inhibitors 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

490-496

Subventions

Organisme : NIAID NIH HHS
ID : U01 AI069911
Pays : United States

Informations de copyright

Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

K.B. reports having received advisory fees and research grant funding from Gilead Sciences. S.K.G. reports having received advisory fees from Gilead Sciences and ViiV Healthcare and an unrestricted grant related to use of dolutegravir from ViiV Healthcare. The remaining authors have no conflicts of interest to disclose.

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Auteurs

Kassem Bourgi (K)

Division of Infectious Diseases, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN.

Susan Ofner (S)

Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN.

Beverly Musick (B)

Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN.

Bradley Griffith (B)

Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN.

Lameck Diero (L)

College of Health Sciences, Moi University School of Medicine, Eldoret, Kenya; and.

Kara Wools-Kaloustian (K)

Division of Infectious Diseases, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN.

Constantin T Yiannoutsos (CT)

Department of Biostatistics and Health Data Science, R.M. Fairbanks School of Public Health, Indiana University, Indianapolis, IN.

Samir K Gupta (SK)

Division of Infectious Diseases, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN.

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