Plasma Level of ATPase Inhibitory Factor 1 and Intrinsic Capacity in Community-Dwelling Older Adults: Prospective Data From the MAPT Study

Author:

da Silva Jaqueline Aragoni1ORCID,Martinez Laurent O2ORCID,Rolland Yves13ORCID,Najib Souad2ORCID,Croyal Mikaël45ORCID,Perret Bertrand2ORCID,Jabrane-Ferrat Nabila6ORCID,El Costa Hicham6ORCID,Guyonnet Sophie13ORCID,Vellas Bruno13ORCID,de Souto Barreto Philipe13ORCID,

Affiliation:

1. Institut du Vieillissement, Gérontopôle de Toulouse, Centre Hospitalo-Universitaire de Toulouse , Toulouse , France

2. LiMitAging, Institut des Maladies Métaboliques et Cardiovasculaires, I2MC, Université de Toulouse, INSERM, Université Toulouse III - Paul Sabatier (UPS) , Toulouse , France

3. CERPOP UMR 1295, University of Toulouse III, INSERM, UPS , Toulouse , France

4. Nantes Université, CHU Nantes, CNRS, INSERM, l’institut du Thorax, BioCore, US16, SFR Bonamy , F-44000 Nantes , France

5. CRNH-Ouest Mass Spectrometry Core Facility , Nantes , France

6. Toulouse Institute for Infectious and Inflammatory Diseases (Infinity), INSERM-CNRS-University Toulouse III , Toulouse , France

Abstract

Abstract Background Intrinsic capacity (IC) is a concept related to functionality that reflects healthy aging. ATPase inhibitory factor 1 (IF1) is a multifaceted protein that regulates mitochondrial oxidative phosphorylation (OXPHOS), and may be involved in IC. The objective of this study is to investigate the association between plasma levels of IF1 and IC changes in community-dwelling older adults. Methods Community-dwelling older adults from the Multidomain Alzheimer Preventive Trial (MAPT Study) were enrolled in this study. A composite IC score was calculated based on 4 IC domains: locomotion, psychological dimension, cognition, and vitality (with data available annually over 4 years of follow-up). Secondary analyses were conducted on the sensory domain (with data available only for 1 year of follow-up). Mixed-model linear regression adjusted for confounders was conducted. Results A total of 1 090 participants with usable IF1 values were included in the study (75.3 ± 4.4 years; 64% females). Compared to the lowest quartile, both the low– and high–intermediate IF1 quartiles were found to be cross-sectionally associated with greater composite IC scores across 4 domains (βlow–intermediate, 1.33; 95% confidence interval [CI] 0.06–2.60 and βhigh–intermediate, 1.78; 95% CI 0.49–3.06). In the secondary analyses, the highest quartile was found to be associated with a slower decline in composite IC scores across 5 domains over 1 year (βhigh 1.60; 95% CI 0.06–3.15). The low– and high–intermediate IF1 quartiles were also found to be cross-sectionally associated with greater locomotion (βlow–intermediate, 2.72; 95% CI 0.36–5.08) and vitality scores (βhigh–intermediate, 1.59; 95% CI 0.06–3.12), respectively. Conclusions This study is the first to demonstrate that levels of circulating IF1, a mitochondrial-related biomarker, are associated with IC composite scores in both cross-sectional and prospective analyses among community-dwelling older adults. However, further research is needed to confirm these findings and elucidate the potential underlying mechanisms that may explain these associations.

Funder

Region Occitanie/Pyrénées-Méditerranée

European Regional Development Fund

Alzheimer Prevention in Occitania and Catalonia

Saint Louis University

Gérontopôle of Toulouse

French Ministry of Health

Pierre Fabre Research Institute

ExonHit Therapeutics SA

Avid Radiopharmaceuticals Inc

University Hospital Center of Toulouse

Association Monegasque pour la Recherche sur la maladie d’Alzheimer

INSERM-University of Toulouse III UMR 1295 (CERPOP) Research Unit

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Aging

Reference35 articles.

1. Operationalising the concept of intrinsic capacity in clinical settings;de Carvalho,2017

2. Mitochondrial dysfunction and intrinsic capacity: insights from a narrative review;Silva;J Gerontol A Biol Sci Med Sci.,2023

3. The hallmarks of aging;López-Otín;Cell.,2013

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