Evidence map›Paper›PMID 39604062›Full record

ArticleJournal of the International AIDS Society2024

Impact of switching to a dolutegravir-based regimen on body weight changes: insights from West African adult HIV cohorts.

Thierry Tiendrebeogo, Karen Malateste, Armel Poda, Albert Minga, Cecile D Lahiri, Oliver Ezechi, Didier K Ekouevi, Igho Ofotokun, Antoine Jaquet, IeDEA West Africa Collaboration

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Article in Journal of the International AIDS Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

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0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Thierry TiendrebeogoUniversity of Bordeaux, National Institute for Health and Medical Research (INSERM) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Research Centre, Bordeaux, France.ORCID https://orcid.org/0000-0002-9393-9732
Karen MalatesteUniversity of Bordeaux, National Institute for Health and Medical Research (INSERM) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Research Centre, Bordeaux, France.
Armel PodaDepartment of Infectious Diseases, Université Nazi Boni, Bobo-Dioulasso, Burkina Faso.
Albert MingaCentre médical de Suivi des Donneurs de Sang (CMSDS), Centre National de Transfusion Sanguine Côte d'Ivoire (CNTSCI), Abidjan, Côte d'Ivoire.ORCID https://orcid.org/0009-0005-7139-2026
Cecile D LahiriDivision of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
Oliver EzechiOffice of the Central Secretariat, Nigeria Institute for Medical Research, Lagos, Nigeria.
Didier K EkoueviUniversity of Bordeaux, National Institute for Health and Medical Research (INSERM) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Research Centre, Bordeaux, France.
Igho OfotokunDivision of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
Antoine JaquetUniversity of Bordeaux, National Institute for Health and Medical Research (INSERM) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Research Centre, Bordeaux, France.
IeDEA West Africa Collaboration

Funding

WADA (West Africa Database on Antiretroviral Therapy) CollaborationU01AI069919 · NIAID · UNIVERSITY OF BORDEAUX II · PI Didier Koumavi Ekouevi, Antoine Jaquet · 2006 to 2026
$29.9M
Neuro HPA Project 1U54AG062334 · NIA · EMORY UNIVERSITY · PI Cecile Delille Lahiri, Vasiliki Michopoulos · 2018 to 2026
$12.2M
Vascular risk after kidney transplantationR01DK069919 · NIDDK · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI LARSEN, JENNIFER L · 2006 to 2010
$2.7M
Eunice Kennedy Shriver National Institute of Child Health and Human Development U01AI069919FIC NIH HHS U01AI069919National Institute of Allergy and Infectious Diseases U01AI069919NCI NIH HHS U01AI069919NHLBI NIH HHS U01AI069919NIAAA NIH HHS U01AI069919NIAID NIH HHS U01 AI069919NIA NIH HHS U54 AG062334NIDA NIH HHS U01AI069919NIDDK NIH HHS U01AI069919U.S. National Institutes of Health, National Institute of Allergy and Infectious Diseases U01AI069919
6 · The paper itself

Abstract

introductionAdverse metabolic effects related to dolutegravir (DTG) are increasingly reported as countries are adopting DTG-based regimens as first-line antiretroviral therapy (ART), but there is limited data from sub-Saharan Africa. We explored changes in body weight pre- and post-switch to a DTG-based regimen and assessed the association between DTG switch and significant weight gain (SWG) defined as a ≥10% increase over a 12-month period in people living with HIV (PLHIV) on ART in West Africa.

methodsWe first included all PLHIV followed in the IeDEA West Africa cohorts between January 2017 and June 2021, with a documented switch to DTG during 2019-2021 and in care ≥36 months at the day of switch. Weight change was estimated using a two slope piecewise linear mixed model with change point at the switch date. Secondly, we emulated a sequence of target trials (ETT) based on the observational data, performing pooled logistic regression analysis to compare SWG occurrence between PLHIV who switched to DTG and those who did not.

resultsWe first included 6705 PLHIV from Burkina Faso, Côte d'Ivoire and Nigeria. Their median age at the time of switch was 48 years (IQR: 42-54) with a median follow-up of 9 years (IQR: 6-12), 63% were female. Most patients switched from efavirenz (EFV)-based ART (56.6%) and nevirapine (NVP)-based ART (30.9%). The overall post-switch annual average weight gain (AAWG) was significantly elevated at 3.07 kg/year [95% CI: 2.33-3.80] compared to the pre-switch AWG which stood at 0.62 kg/year [95% CI: 0.36-0.88]. The post-switch AWG was greater in patients previously on EFV and protease inhibitor (PI)-based ART compared to those on NVP-based ART. The pooled logistic regression analyses of a sequence of 24 ETT, including 9598 person-trials, switching to DTG was significantly associated with an SWG (aOR = 2.54; 95% CI = 2.18-2.97).

conclusionsIn West Africa, a 12-month DTG exposure was associated with substantial weight gain, especially in PLHIV previously on EFV and PI-based ARTs. Continuous weight monitoring and metabolic profiling is imperative in HIV cohorts to delineate the long-term cardiometabolic impact of DTG as patients with, or at elevated risk for cardiovascular diseases might benefit from alternative ART regimens.

Indexed as

Heterocyclic Compounds, 3-RingHIV InfectionsOxazinesPiperazinesPyridonesWeight GainAdultAfrica, WesternAlkynesAnti-HIV AgentsBenzoxazinesBody WeightCohort StudiesCote d'IvoireCyclopropanesDolutegravirAlkynesAnti-HIV AgentsBenzoxazinesCyclopropanesDolutegravirefavirenzHeterocyclic Compounds, 3-RingHIV Integrase InhibitorsNevirapineOxazinesPiperazinesPyridonesantiretroviral therapydolutegravirHIVobservational cohort studyweight gainWest Africa

Identifiers

PMID39604062
PMCPMC11602402

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.