Regional variation in weight change after the transition to dolutegravir: a prospective cohort study in Uganda and South Africa.


Journal

AIDS (London, England)
ISSN: 1473-5571
Titre abrégé: AIDS
Pays: England
ID NLM: 8710219

Informations de publication

Date de publication:
20 Mar 2024
Historique:
medline: 20 3 2024
pubmed: 20 3 2024
entrez: 20 3 2024
Statut: aheadofprint

Résumé

People with HIV (PWH) on integrase inhibitor-based regimens may be at risk of excess weight gain, but it is unclear if this risk is consistent across settings. We assessed weight change over 48 weeks among PWH who were transitioned to tenofovir disoproxil fumarate/lamivudine/dolutegravir (TLD). We conducted a prospective cohort study at public-sector HIV clinics in Uganda and South Africa. Eligible participants were adults who were transitioned to TLD. Weight was measured at enrollment, 24-, and 48-weeks post TLD transition. Our outcomes were (1) weight change, (2) change in waist circumference, and (3) clinically significant weight gain, defined as ≥10% increase in weight from baseline, over 48 weeks. We used linear mixed-effects regression models, adjusted for demographic factors, to estimate weight gain and identify risk factors. Weight data were available for 428 participants in Uganda and 367 in South Africa. The mean weight change was 0.6 kg [95%CI: 0.1-1.0] in Uganda and 2.9 kg [2.3-3.4] in South Africa (p < 0.001). The mean change in waist circumference was 0.8 cm [95%CI: 0.0-1.5]) in Uganda and 2.3 cm [95%CI: 1.4-3.2] in South Africa (p = 0.012). Clinically significant weight gain occurred in 9.8% [7.0-12.6] of participants in Uganda and 18.0% [14.1-21.9] in South Africa (p < 0.001). After adjustment, PWH gained significantly less weight in Uganda than in South Africa. PWH in South Africa experienced significantly greater weight gain and increases in waist circumference compared to Uganda. Strategies to address weight gain in PWH should be carefully considered and may vary by region.

Sections du résumé

BACKGROUND BACKGROUND
People with HIV (PWH) on integrase inhibitor-based regimens may be at risk of excess weight gain, but it is unclear if this risk is consistent across settings. We assessed weight change over 48 weeks among PWH who were transitioned to tenofovir disoproxil fumarate/lamivudine/dolutegravir (TLD).
DESIGN METHODS
We conducted a prospective cohort study at public-sector HIV clinics in Uganda and South Africa.
METHODS METHODS
Eligible participants were adults who were transitioned to TLD. Weight was measured at enrollment, 24-, and 48-weeks post TLD transition. Our outcomes were (1) weight change, (2) change in waist circumference, and (3) clinically significant weight gain, defined as ≥10% increase in weight from baseline, over 48 weeks. We used linear mixed-effects regression models, adjusted for demographic factors, to estimate weight gain and identify risk factors.
RESULTS RESULTS
Weight data were available for 428 participants in Uganda and 367 in South Africa. The mean weight change was 0.6 kg [95%CI: 0.1-1.0] in Uganda and 2.9 kg [2.3-3.4] in South Africa (p < 0.001). The mean change in waist circumference was 0.8 cm [95%CI: 0.0-1.5]) in Uganda and 2.3 cm [95%CI: 1.4-3.2] in South Africa (p = 0.012). Clinically significant weight gain occurred in 9.8% [7.0-12.6] of participants in Uganda and 18.0% [14.1-21.9] in South Africa (p < 0.001). After adjustment, PWH gained significantly less weight in Uganda than in South Africa.
CONCLUSIONS CONCLUSIONS
PWH in South Africa experienced significantly greater weight gain and increases in waist circumference compared to Uganda. Strategies to address weight gain in PWH should be carefully considered and may vary by region.

Identifiants

pubmed: 38507584
doi: 10.1097/QAD.0000000000003888
pii: 00002030-990000000-00463
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.

Auteurs

Richard Migisha (R)

Mbarara University of Science and Technology, Mbarara, Uganda.

Geoffrey Chen (G)

Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.

Winnie R Muyindike (WR)

Mbarara University of Science and Technology, Mbarara, Uganda.

Taing Nandi Aung (TN)

Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.

Victoria Nanfuka (V)

Mbarara University of Science and Technology, Mbarara, Uganda.

Nimusiima Komukama (N)

Mbarara University of Science and Technology, Mbarara, Uganda.

Nomathemba Chandiwana (N)

Wits Ezintsha, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Gugulethu Shazi (G)

Africa Health Research Institute, Durban, South Africa.

Dessie Tien (D)

Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.

Mahomed-Yunus S Moosa (MS)

Department of Infectious Diseases, University of KwaZulu-Natal, Durban, South Africa.

Ravindra K Gupta (RK)

Africa Health Research Institute, Durban, South Africa.
University of Cambridge, Cambridge, United Kingdom.

Deenan Pillay (D)

University College London, London, United Kingdom.

Vincent C Marconi (VC)

Emory University School of Medicine and Rollins School of Public Health, Emory University, Atlanta, GA, USA.

Bethany Hedt-Gauthier (B)

Harvard Medical School, Boston, MA, USA.

Willem D F Venter (WDF)

Wits Ezintsha, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Mark J Siedner (MJ)

Mbarara University of Science and Technology, Mbarara, Uganda.
Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.
Africa Health Research Institute, Durban, South Africa.
Harvard Medical School, Boston, MA, USA.
Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.

Suzanne M McCluskey (SM)

Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.
Harvard Medical School, Boston, MA, USA.
Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.

Jennifer Manne-Goehler (J)

Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.
Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.
Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA, USA.

Classifications MeSH