Aller au contenu principal
Accès ouvert déclaré 2025 article

Identifying Biomarkers of Frailty Through an Integrated Multi-omics Analysis

0Citations signalées, ce qui n’est pas une note de qualité
1Institutions déclarées
1Pays d’affiliation déclarés

Rattachement africain : us. Niveau de preuve : code pays fourni par la source.

Le résumé fourni par la source

Abstract Background Older adults are vulnerable to frailty, leading to adverse outcomes. We examined baseline metabolomic/proteomic biomarkers associated with different frailty states with a goal of advancing precision medicine in a pilot study of older adults pursuing physical therapy. Methods We conducted a prospective study of 18 adults (≥65 years) from primary care, referred for physical therapy. Frailty was classified using a modified Cumulative Deficit Index (38 variables). Baseline gait speed, grip strength and instrumental activities of daily living (ADL) score (0-100) were assessed. Plasma samples underwent untargeted metabolomics and proteomics. Proteomics used Mag-Net enrichment to detect low-abundance proteins, followed by LC-MS/MS analysis on a Thermo Neo-Orbitrap Astral. Metabolomics involved methanol extraction and CE-MS/MS analysis using a 908Devices ZipChip-Thermo Fusion Lumos. Results The mean participant age was 77.1±5.5 (33% female). There were 12 were pre-frail and 6 frail participants. Baseline function differed between groups: gait speed was 1.23±0.26 vs. 0.98±0.21 m/s (p = 0.01), grip strength was 28.8±9.5 vs. 27.1±5.6kg (p = 0.98), and instrumental ADL scores were 100±0 vs. 66.1±22.9 (p = 0.005). Among 4,300 quantified proteins, ∼60 differed (p < 0.05; log2-fold change ±0.5) with ∼40 proteins elevated in frail individuals, including nucleosome-related proteins (H2B, H3C1, H2AC3, H3-4). Metabolomic analysis assessed ∼275 metabolites quantifying 115. Nicotinamide was significantly downregulated in the frail group (p < 0.05; log2-fold <-0.5). Conclusions This pilot study suggests that circulating nucleosomes–complexes of histones and DNA–may serve as biomarkers for aging and related conditions. Additionally, nicotinamide, a precursor of NAD4, a key coenzyme in metabolism, DNA repair, and mitochondrial function, declines with age, potentially contributing to age-related conditions.

Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.

Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Identifying Biomarkers of Frailty Through an Integrated Multi-omics Analysis
Date Crossref
01/12/2025
Éditeur
Oxford University Press (OUP)
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Les institutions déclarées

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

Frailty in Older AdultsMetabolomics and Mass Spectrometry StudiesHealth, Environment, Cognitive Aging

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.