Relationships Between Hepatic Steatosis and Frailty Differ by HIV Serostatus.


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:
01 Oct 2024
Historique:
received: 04 03 2024
accepted: 16 05 2024
medline: 9 9 2024
pubmed: 9 9 2024
entrez: 9 9 2024
Statut: ppublish

Résumé

Frailty is associated with obesity-related comorbidities, but the relationship with nonalcoholic fatty liver disease (NAFLD) in people with HIV has been incompletely described. Our objective was to assess the associations between NAFLD and frailty. Cross-sectional and longitudinal analysis of men in the Multicenter AIDS Cohort Study. NAFLD was defined as a liver/spleen ratio <1.0 on abdominal computed tomography scans; frailty was defined by the frailty phenotype as having 3 of the following: weakness, slowness, weight loss, exhaustion, and low physical activity. Men without (n = 200) and with HIV (n = 292) were included. NAFLD prevalence was 21% vs 16% and frailty 12% vs 17%, respectively. Among men with NAFLD, frailty was more prevalent in men without HIV (21% vs 11%). In multivariate analysis, NAFLD was significantly associated with frailty after controlling for significant variables. Men without HIV and NAFLD had 2.6 times higher probability [95% confidence interval (CI): 1.2- to 5.7] of frailty relative to men with neither HIV nor NAFLD. This association was not seen in men with HIV. The probability of frailty was higher among men without HIV with NAFLD (27% vs 10% in men without NAFLD) but lower among men with HIV with NAFLD (14% vs 19% in men without NAFLD). No significant relationships were found in longitudinal analyses. NAFLD was independently associated with frailty among men without HIV but not men with HIV, despite increased prevalence of frailty among men with HIV. The mechanisms of the muscle-liver-adipose tissue axis underlying NAFLD might differ by HIV serostatus.

Sections du résumé

BACKGROUND BACKGROUND
Frailty is associated with obesity-related comorbidities, but the relationship with nonalcoholic fatty liver disease (NAFLD) in people with HIV has been incompletely described. Our objective was to assess the associations between NAFLD and frailty.
METHODS METHODS
Cross-sectional and longitudinal analysis of men in the Multicenter AIDS Cohort Study. NAFLD was defined as a liver/spleen ratio <1.0 on abdominal computed tomography scans; frailty was defined by the frailty phenotype as having 3 of the following: weakness, slowness, weight loss, exhaustion, and low physical activity.
RESULTS RESULTS
Men without (n = 200) and with HIV (n = 292) were included. NAFLD prevalence was 21% vs 16% and frailty 12% vs 17%, respectively. Among men with NAFLD, frailty was more prevalent in men without HIV (21% vs 11%). In multivariate analysis, NAFLD was significantly associated with frailty after controlling for significant variables. Men without HIV and NAFLD had 2.6 times higher probability [95% confidence interval (CI): 1.2- to 5.7] of frailty relative to men with neither HIV nor NAFLD. This association was not seen in men with HIV. The probability of frailty was higher among men without HIV with NAFLD (27% vs 10% in men without NAFLD) but lower among men with HIV with NAFLD (14% vs 19% in men without NAFLD). No significant relationships were found in longitudinal analyses.
CONCLUSIONS CONCLUSIONS
NAFLD was independently associated with frailty among men without HIV but not men with HIV, despite increased prevalence of frailty among men with HIV. The mechanisms of the muscle-liver-adipose tissue axis underlying NAFLD might differ by HIV serostatus.

Identifiants

pubmed: 39250650
doi: 10.1097/QAI.0000000000003477
pii: 00126334-202410010-00009
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

165-171

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK126042
Pays : United States
Organisme : NIA NIH HHS
ID : K24 AG082527
Pays : United States

Informations de copyright

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

Déclaration de conflit d'intérêts

The authors have no funding or conflicts of interest to disclose.

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Auteurs

Paula Debroy (P)

Division of Infectious Diseases, UTHealth Houston, Houston, TX.

Benjamin W Barrett (BW)

Department of Endocrinology, Johns Hopkins University, Baltimore, MD.

Kristine M Erlandson (KM)

Division of Infectious Diseases, University of Colorado Anschutz Medical Center, Aurora, CO.

Matthew Budoff (M)

The Lundquist Institute, Torrence, CA.

Todd T Brown (TT)

Department of Endocrinology, Johns Hopkins University, Baltimore, MD.

Jennifer C Price (JC)

Division of Hepatology, University of California San Francisco, San Francisco, CA.

Wendy S Post (WS)

Department of Endocrinology, Johns Hopkins University, Baltimore, MD.

Valentina Stosor (V)

Division of Infectious Diseases, Northwestern University, Evanston, IL; and.

Carling Skavarca (C)

Department of Infectious Diseases and Microbiology University of Pittsburgh, Pittsburgh, PA.

Gypsyamber D'Souza (G)

Department of Endocrinology, Johns Hopkins University, Baltimore, MD.

Jordan E Lake (JE)

Division of Infectious Diseases, UTHealth Houston, Houston, TX.

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