Plasma acylcarnitine levels increase with healthy aging.


Journal

Aging
ISSN: 1945-4589
Titre abrégé: Aging (Albany NY)
Pays: United States
ID NLM: 101508617

Informations de publication

Date de publication:
16 06 2020
Historique:
received: 21 02 2020
accepted: 27 05 2020
pubmed: 20 6 2020
medline: 9 3 2021
entrez: 20 6 2020
Statut: ppublish

Résumé

Acylcarnitines transport fatty acids into mitochondria and are essential for β-oxidation and energy metabolism. Decreased mitochondrial activity results in increased plasma acylcarnitines, and increased acylcarnitines activate proinflammatory signaling and associate with age-related disease. Changes in acylcarnitines associated with healthy aging, however, are not well characterized. In the present study, we examined the associations of plasma acylcarnitines with age (range: 20-90) in 163 healthy, non-diseased individuals from the predictive medicine research cohort (NCT00336570) and tested for gender-specific differences. The results show that long-chain and very long-chain acylcarnitines increased with age, while many odd-chain acylcarnitines decreased with age. Gender-specific differences were observed for several acylcarnitines, e.g., eicosadienoylcarnitine varied with age in males, and hydroxystearoylcarnitine varied in females. Metabolome-wide association study (MWAS) of age-associated acylcarnitines with all untargeted metabolic features showed little overlap between genders. These results show that plasma concentrations of acylcarnitines vary with age and gender in individuals selected for criteria of health. Whether these variations reflect mitochondrial dysfunction with aging, mitochondrial reprogramming in response to chronic environmental exposures, early pre-disease change, or an adaptive response to healthy aging, is unclear. The results highlight a potential utility for untargeted metabolomics research to elucidate gender-specific mechanisms of aging and age-related disease.

Identifiants

pubmed: 32554854
pii: 103462
doi: 10.18632/aging.103462
pmc: PMC7377890
doi:

Substances chimiques

acylcarnitine 0
Carnitine S7UI8SM58A

Banques de données

ClinicalTrials.gov
['NCT00336570']

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

13555-13570

Subventions

Organisme : NIEHS NIH HHS
ID : R01 ES023485
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008602
Pays : United States
Organisme : NIH HHS
ID : S10 OD018006
Pays : United States

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Auteurs

Zachery R Jarrell (ZR)

Division of Pulmonary, Allergy and Critical Care Medicine, Atlanta, GA 30322, USA.

M Ryan Smith (MR)

Division of Pulmonary, Allergy and Critical Care Medicine, Atlanta, GA 30322, USA.

Xin Hu (X)

Division of Pulmonary, Allergy and Critical Care Medicine, Atlanta, GA 30322, USA.

Michael Orr (M)

Division of Pulmonary, Allergy and Critical Care Medicine, Atlanta, GA 30322, USA.

Ken H Liu (KH)

Division of Pulmonary, Allergy and Critical Care Medicine, Atlanta, GA 30322, USA.

Arshed A Quyyumi (AA)

Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA.

Dean P Jones (DP)

Division of Pulmonary, Allergy and Critical Care Medicine, Atlanta, GA 30322, USA.

Young-Mi Go (YM)

Division of Pulmonary, Allergy and Critical Care Medicine, Atlanta, GA 30322, USA.

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Classifications MeSH