The metabolome as a biomarker of aging in Drosophila melanogaster.


Journal

Aging cell
ISSN: 1474-9726
Titre abrégé: Aging Cell
Pays: England
ID NLM: 101130839

Informations de publication

Date de publication:
02 2022
Historique:
received: 30 08 2021
accepted: 12 11 2021
pubmed: 13 1 2022
medline: 5 4 2022
entrez: 12 1 2022
Statut: ppublish

Résumé

Many biomarkers have been shown to be associated not only with chronological age but also with functional measures of biological age. In human populations, it is difficult to show whether variation in biological age is truly predictive of life expectancy, as such research would require longitudinal studies over many years, or even decades. We followed adult cohorts of 20 Drosophila Genetic Reference Panel (DGRP) strains chosen to represent the breadth of lifespan variation, obtain estimates of lifespan, baseline mortality, and rate of aging, and associate these parameters with age-specific functional traits including fecundity and climbing activity and with age-specific targeted metabolomic profiles. We show that activity levels and metabolome-wide profiles are strongly associated with age, that numerous individual metabolites show a strong association with lifespan, and that the metabolome provides a biological clock that predicts not only sample age but also future mortality rates and lifespan. This study with 20 genotypes and 87 metabolites, while relatively small in scope, establishes strong proof of principle for the fly as a powerful experimental model to test hypotheses about biomarkers and aging and provides further evidence for the potential value of metabolomic profiles as biomarkers of aging.

Identifiants

pubmed: 35019203
doi: 10.1111/acel.13548
pmc: PMC8844127
doi:

Substances chimiques

Biomarkers 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13548

Subventions

Organisme : NIGMS NIH HHS
ID : R24 GM141156
Pays : United States
Organisme : NIGMS NIH HHS
ID : R24GM141156
Pays : United States
Organisme : NIEHS NIH HHS
ID : U2CES030167
Pays : United States
Organisme : NIGMS NIH HHS
ID : P41 GM103533
Pays : United States
Organisme : NIGMS NIH HHS
ID : P41GM103533
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG013280
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG049494
Pays : United States

Informations de copyright

© 2022 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd.

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Auteurs

Xiaqing Zhao (X)

Department of Lab Medicine and Pathology, University of Washington School of Medicine, Seattle, US.

Forrest T Golic (FT)

Department of Lab Medicine and Pathology, University of Washington School of Medicine, Seattle, US.

Benjamin R Harrison (BR)

Department of Lab Medicine and Pathology, University of Washington School of Medicine, Seattle, US.

Meghna Manoj (M)

Department of Lab Medicine and Pathology, University of Washington School of Medicine, Seattle, US.

Elise V Hoffman (EV)

Department of Lab Medicine and Pathology, University of Washington School of Medicine, Seattle, US.

Neta Simon (N)

Department of Lab Medicine and Pathology, University of Washington School of Medicine, Seattle, US.

Richard Johnson (R)

Department of Genome Sciences, University of Washington School of Medicine, Seattle, US.

Michael J MacCoss (MJ)

Department of Genome Sciences, University of Washington School of Medicine, Seattle, US.

Lauren M McIntyre (LM)

Genetics Institute, University of Florida, Gainesville, USA.
Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, USA.

Daniel E L Promislow (DEL)

Department of Lab Medicine and Pathology, University of Washington School of Medicine, Seattle, US.
Department of Biology, University of Washington, Seattle, US.

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Classifications MeSH