Lean mass declines consistently over 10 years in people living with HIV on antiretroviral therapy, with patterns differing by sex.


Journal

Antiviral therapy
ISSN: 2040-2058
Titre abrégé: Antivir Ther
Pays: England
ID NLM: 9815705

Informations de publication

Date de publication:
2019
Historique:
accepted: 18 03 2019
pubmed: 30 4 2019
medline: 7 7 2020
entrez: 30 4 2019
Statut: ppublish

Résumé

The long-term trajectory of and factors affecting lean mass in people living with HIV (PLWH) are incompletely described. PLWH in the Modena HIV Metabolic Cohort underwent dual-energy X-ray absorptiometry (DXA) scans every 6-12 months for up to 10 years (median 4.6 scans). Mixed effect regression modelling in combined and sex-stratified models determined annual rates of and clinical factors significantly associated with appendicular lean mass (ALM). A total of 839 women and 1,759 men contributing ≥2 DXA scans had baseline median age 44 years and 14 years since HIV diagnosis; 76% were virologically suppressed on antiretroviral therapy (ART). Baseline median ALM was 16.9 kg for women and 24.8 kg for men. ALM decreased during the study period, with mean yearly ALM loss of -231 g in women and -322 g in men. Less ALM was associated with female sex, age >50 years, detectable HIV-1 RNA, and tenofovir and integrase inhibitor use. Greater ALM was associated with longer ART duration. In sex-stratified models, relationships between ALM and total ART duration and integrase inhibitor use were not significant for women, but the relationship with tenofovir use persisted. For men, AIDS wasting and CD4 ALM steadily declined over time in this cohort of PLWH on ART that included a large number of women. HIV- and ART-specific risk factors emerged that varied by sex. The observed associations between tenofovir or integrase inhibitor use and lower ALM particularly warrant further study.

Sections du résumé

BACKGROUND
The long-term trajectory of and factors affecting lean mass in people living with HIV (PLWH) are incompletely described.
METHODS
PLWH in the Modena HIV Metabolic Cohort underwent dual-energy X-ray absorptiometry (DXA) scans every 6-12 months for up to 10 years (median 4.6 scans). Mixed effect regression modelling in combined and sex-stratified models determined annual rates of and clinical factors significantly associated with appendicular lean mass (ALM).
RESULTS
A total of 839 women and 1,759 men contributing ≥2 DXA scans had baseline median age 44 years and 14 years since HIV diagnosis; 76% were virologically suppressed on antiretroviral therapy (ART). Baseline median ALM was 16.9 kg for women and 24.8 kg for men. ALM decreased during the study period, with mean yearly ALM loss of -231 g in women and -322 g in men. Less ALM was associated with female sex, age >50 years, detectable HIV-1 RNA, and tenofovir and integrase inhibitor use. Greater ALM was associated with longer ART duration. In sex-stratified models, relationships between ALM and total ART duration and integrase inhibitor use were not significant for women, but the relationship with tenofovir use persisted. For men, AIDS wasting and CD4
CONCLUSIONS
ALM steadily declined over time in this cohort of PLWH on ART that included a large number of women. HIV- and ART-specific risk factors emerged that varied by sex. The observed associations between tenofovir or integrase inhibitor use and lower ALM particularly warrant further study.

Identifiants

pubmed: 31032811
doi: 10.3851/IMP3312
pmc: PMC6819205
mid: NIHMS1032892
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

383-387

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

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Auteurs

Paula Debroy (P)

Division of Infectious Diseases, University of Texas Health Sciences Center, Houston, TX, USA.

Jordan E Lake (JE)

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

Myung Sim (M)

Division of Infectious Diseases, University of California Los Angeles, Los Angeles, CA, USA.

Kristine M Erlandson (KM)

Division of Infectious Diseases, University of Colorado, Aurora, CO, USA.

Julian Falutz (J)

Division of Geriatrics, McGill University, Montreal, QC, Canada.

Carla M Prado (CM)

Division of Human Nutrition, University of Alberta, Edmonton, AB, Canada.

Todd T Brown (TT)

Division of Endocrinology, Diabetes, and Metabolism, Johns Hopkins University, Baltimore, MD, USA.

Giovanni Guaraldi (G)

Department of Medical and Surgical Sciences for Children & Adults, University of Modena and Reggio Emilia, Modena, Italy.

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Classifications MeSH