Progressive increases in fat mass occur in adults living with HIV on antiretroviral therapy, but patterns differ by sex and anatomic depot.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
01 04 2019
Historique:
received: 12 08 2018
revised: 21 11 2018
accepted: 28 11 2018
pubmed: 23 1 2019
medline: 26 6 2020
entrez: 23 1 2019
Statut: ppublish

Résumé

Although weight gain on ART is common, the long-term trajectory of and factors affecting increases in fat mass in people living with HIV are not well described. Men and women living with HIV in the Modena HIV Metabolic Clinic underwent DXA scans every 6-12 months for up to 10 years (median 4.6 years). Regression modelling in both combined and sex-stratified models determined changes in and clinical factors significantly associated with trunk and leg fat mass over the study period. A total of 839 women and 1759 men contributed two or more DXA scans. The baseline median age was 44 years and BMI 22.9 kg/m2; 76% were virologically suppressed on ART at baseline. For both sexes, trunk and leg fat consistently increased over the study period, with mean yearly trunk and leg fat gain of 3.6% and 7.5% in women and 6.3% and 10.8% in men, respectively. In multivariate analysis, factors associated with greater fat mass included female sex, per-year ART use (specifically tenofovir disoproxil fumarate and integrase strand transfer inhibitor therapy), per-unit BMI increase, no self-reported physical activity and CD4 nadir <200 cells/mm3. Among people living with HIV on ART, trunk and leg fat mass increased steadily over a median of 4.6 years of follow up, particularly among women. After controlling for traditional risk factors, HIV- and ART-specific risk factors emerged.

Identifiants

pubmed: 30668716
pii: 5296293
doi: 10.1093/jac/dky551
pmc: PMC6419613
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1028-1034

Subventions

Organisme : NIA NIH HHS
ID : K23 AG050260
Pays : United States
Organisme : NIAID NIH HHS
ID : K23 AI110532
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI120834
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG054366
Pays : United States

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.

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Auteurs

Paula Debroy (P)

University of Texas Health Sciences Center, Houston, TX, USA.

Myung Sim (M)

University of California Los Angeles, Los Angeles, CA, USA.

Kristine M Erlandson (KM)

University of Colorado, Aurora, CO, USA.

Julian Falutz (J)

McGill University, Montreal, Canada.

Carla M Prado (CM)

Hospital Beatriz Ângelo, Loures, Portugal.

Todd T Brown (TT)

Johns Hopkins University, Baltimore, MD, USA.

Giovanni Guaraldi (G)

University of Modena and Reggio Emilia, Modena, Italy.

Jordan E Lake (JE)

University of Texas Health Sciences Center, Houston, TX, USA.
University of California Los Angeles, Los Angeles, CA, USA.

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Classifications MeSH