Language

English

Publication Date

3-7-2025

Journal

The Journals of Gerontology: Series A

DOI

10.1093/gerona/glae251

PMID

39447036

PMCID

PMC11949428

PubMedCentral® Posted Date

10-24-2024

PubMedCentral® Full Text Version

Post-print

Abstract

Obesity accelerates the onset and progression of age-related conditions. In preclinical models, obesity drives cellular senescence, a cell fate that compromises tissue health and function, in part through a robust and diverse secretome. In humans, components of the secretome have been used as senescence biomarkers that are predictive of age-related disease, disability, and mortality. Here, using biospecimens and clinical data from two large and independent cohorts of older adults, we tested the hypothesis that the circulating concentrations of senescence biomarkers are influenced by body mass index. After adjusting for age, sex, and race, we observed significant increases in activin A, Fas, MDC, PAI1, PARC, TNFR1, and VEGFA, and a significant decrease in RAGE, from normal weight, to overweight, to obesity body mass index categories by linear regression in both cohorts (all p <  .05). These results highlight the influence of body mass index on circulating concentrations of senescence biomarkers.

Keywords

Humans, Body Mass Index, Biomarkers, Aged, Female, Male, Cellular Senescence, Obesity, Aging, Aged, 80 and over, Middle Aged, Body mass index, Cellular senescence, Obesity, Senescence-associated secretory phenotype

Published Open-Access

yes

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