<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Brodeau C</submitter><funding>INSPIRE Program</funding><funding>IHU HealthAge of Toulouse (French National Research Agency (ANR) as part of the France 2030 program</funding><funding>Programme d'Investissements d'Avenir and the Agence Nationale pour la Recherche for the national infrastructure ECELLFrance</funding><funding>EUR CARe</funding><pagination>e70153</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12419852</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(9)</volume><pubmed_abstract>Aging leads to a decline in physiological reserves, an increase in age-related diseases, reduced functional ability and a shortened healthspan. While molecular markers of chronological aging exist, their link to general health and intrinsic capacity (IC), a composite measure of physical and mental capacities, remains unclear. This study integrates the WHO's Healthy Aging framework with geroscience to explore fibroblasts as indicators of health. We assessed primary skin fibroblasts from 133 individuals aged 20-96, evaluating their ability to maintain tissue structure, modulate immune responses and regulate metabolism (SIM functions). By combining functional and molecular analyses, we investigated the relationship between fibroblast performance, chronological age and IC. Our results demonstr</pubmed_abstract><journal>Aging cell</journal><pubmed_title>Identification of Functional Cellular Markers Related to Human Health, Frailty and Chronological Age.</pubmed_title><pmcid>PMC12419852</pmcid><funding_grant_id>ANR 23-IAHU-0011</funding_grant_id><funding_grant_id>ANR-18-EURE-0003</funding_grant_id><funding_grant_id>1901175</funding_grant_id><funding_grant_id>PIA-ANR-11-INBS-005</funding_grant_id><funding_grant_id>MP0022856</funding_grant_id><pubmed_authors>Joly C</pubmed_authors><pubmed_authors>Yart A</pubmed_authors><pubmed_authors>Ader I</pubmed_authors><pubmed_authors>Tanner KT</pubmed_authors><pubmed_authors>Cohen AA</pubmed_authors><pubmed_authors>Espagnolle N</pubmed_authors><pubmed_authors>de Souto Barreto P</pubmed_authors><pubmed_authors>Nakhle J</pubmed_authors><pubmed_authors>Carriere A</pubmed_authors><pubmed_authors>Blase V</pubmed_authors><pubmed_authors>Fassy J</pubmed_authors><pubmed_authors>Lu WH</pubmed_authors><pubmed_authors>Teste O</pubmed_authors><pubmed_authors>IHU HealthAge/Open Science group</pubmed_authors><pubmed_authors>Chekroun A</pubmed_authors><pubmed_authors>Casteilla L</pubmed_authors><pubmed_authors>Planat V</pubmed_authors><pubmed_authors>Dray C</pubmed_authors><pubmed_authors>Brodeau C</pubmed_authors><pubmed_authors>Tertrais M</pubmed_authors><pubmed_authors>Tremblay-Franco M</pubmed_authors><pubmed_authors>Guyonnet S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of Functional Cellular Markers Related to Human Health, Frailty and Chronological Age.</name><description>Aging leads to a decline in physiological reserves, an increase in age-related diseases, reduced functional ability and a shortened healthspan. While molecular markers of chronological aging exist, their link to general health and intrinsic capacity (IC), a composite measure of physical and mental capacities, remains unclear. This study integrates the WHO's Healthy Aging framework with geroscience to explore fibroblasts as indicators of health. We assessed primary skin fibroblasts from 133 individuals aged 20-96, evaluating their ability to maintain tissue structure, modulate immune responses and regulate metabolism (SIM functions). By combining functional and molecular analyses, we investigated the relationship between fibroblast performance, chronological age and IC. Our results demonstr</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-02T17:43:02.883Z</modification><creation>2026-05-27T03:07:06.537Z</creation></dates><accession>S-EPMC12419852</accession><cross_references><pubmed>40591484</pubmed><doi>10.1111/acel.70153</doi></cross_references></HashMap>