Longitudinal associations between ATPase Inhibitory Factor 1, Growth Differentiation Factor-15, and nutritional status in older adults from the MAPT study.
biomarkers
nutrition
successful aging
Journal
The journals of gerontology. Series A, Biological sciences and medical sciences
ISSN: 1758-535X
Titre abrégé: J Gerontol A Biol Sci Med Sci
Pays: United States
ID NLM: 9502837
Informations de publication
Date de publication:
07 Oct 2023
07 Oct 2023
Historique:
received:
11
01
2023
medline:
7
10
2023
pubmed:
7
10
2023
entrez:
7
10
2023
Statut:
aheadofprint
Résumé
Weight and appetite regulation have been associated with the expression and secretion of ATPase inhibitory factor 1 (IF1) and growth-differentiation factor-15 (GDF-15), two potential biomarkers for age-related mitochondrial dysfunction. The aim was to explore the associations between these biomarkers and nutritional variables in the MAPT study. IF1 and GDF-15 plasma levels were quantified at one-year follow-up. The nutritional status was measured using the Mini Nutritional Assessment (MNA) score variation between baseline and 1- and 2-year visits; appetite loss was extracted from the MNA. Bodyweight was measured every six months until the third year and then yearly until the fifth year of follow-up, and weight loss was established if the loss was greater than 5 or 10 percent within the past 6 or 12 months, respectively. Bidirectional associations of IF1 and GDF-15 levels with malnutrition, appetite and weight loss were examined. The interactions between individual IF1 and GDF-15 with sex were explored. 448 participants had MNA data and 1045 had weight loss data. All the associations between IF1 levels and the MNA score, appetite loss, and weight loss were non-significant. Higher GDF-15 levels were cross-sectionally associated with appetite loss at the first year of follow-up, and the GDF-15 highest quartile was associated with nearly 80% higher risks of weight loss over four years. Interactions between IF1 and GDF-15 levels, and between these two markers and sex were not significantly associated with the outcomes. GDF-15 plasma levels were related to key malnutrition criteria.
Sections du résumé
BACKGROUND
BACKGROUND
Weight and appetite regulation have been associated with the expression and secretion of ATPase inhibitory factor 1 (IF1) and growth-differentiation factor-15 (GDF-15), two potential biomarkers for age-related mitochondrial dysfunction. The aim was to explore the associations between these biomarkers and nutritional variables in the MAPT study.
METHODS
METHODS
IF1 and GDF-15 plasma levels were quantified at one-year follow-up. The nutritional status was measured using the Mini Nutritional Assessment (MNA) score variation between baseline and 1- and 2-year visits; appetite loss was extracted from the MNA. Bodyweight was measured every six months until the third year and then yearly until the fifth year of follow-up, and weight loss was established if the loss was greater than 5 or 10 percent within the past 6 or 12 months, respectively. Bidirectional associations of IF1 and GDF-15 levels with malnutrition, appetite and weight loss were examined. The interactions between individual IF1 and GDF-15 with sex were explored.
RESULTS
RESULTS
448 participants had MNA data and 1045 had weight loss data. All the associations between IF1 levels and the MNA score, appetite loss, and weight loss were non-significant. Higher GDF-15 levels were cross-sectionally associated with appetite loss at the first year of follow-up, and the GDF-15 highest quartile was associated with nearly 80% higher risks of weight loss over four years. Interactions between IF1 and GDF-15 levels, and between these two markers and sex were not significantly associated with the outcomes.
CONCLUSION
CONCLUSIONS
GDF-15 plasma levels were related to key malnutrition criteria.
Identifiants
pubmed: 37804244
pii: 7296475
doi: 10.1093/gerona/glad236
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© The Author(s) 2023. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.