Metabolic Age Based on the BBMRI-NL
aging
cardiovascular disease
data science
metabolomics
Journal
Circulation. Genomic and precision medicine
ISSN: 2574-8300
Titre abrégé: Circ Genom Precis Med
Pays: United States
ID NLM: 101714113
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
entrez:
20
10
2020
pubmed:
21
10
2020
medline:
28
10
2021
Statut:
ppublish
Résumé
The blood metabolome incorporates cues from the environment and the host's genetic background, potentially offering a holistic view of an individual's health status. We have compiled a vast resource of proton nuclear magnetic resonance metabolomics and phenotypic data encompassing over 25 000 samples derived from 26 community and hospital-based cohorts. Using this resource, we constructed a metabolomics-based age predictor (metaboAge) to calculate an individual's biological age. Exploration in independent cohorts demonstrates that being judged older by one's metabolome, as compared with one's chronological age, confers an increased risk on future cardiovascular disease, mortality, and functionality in older individuals. A web-based tool for calculating metaboAge (metaboage.researchlumc.nl) allows easy incorporation in other epidemiological studies. Access to data can be requested at bbmri.nl/samples-images-data. In summary, we present a vast resource of metabolomics data and illustrate its merit by constructing a metabolomics-based score for biological age that captures aspects of current and future cardiometabolic health.
Sections du résumé
BACKGROUND
The blood metabolome incorporates cues from the environment and the host's genetic background, potentially offering a holistic view of an individual's health status.
METHODS
We have compiled a vast resource of proton nuclear magnetic resonance metabolomics and phenotypic data encompassing over 25 000 samples derived from 26 community and hospital-based cohorts.
RESULTS
Using this resource, we constructed a metabolomics-based age predictor (metaboAge) to calculate an individual's biological age. Exploration in independent cohorts demonstrates that being judged older by one's metabolome, as compared with one's chronological age, confers an increased risk on future cardiovascular disease, mortality, and functionality in older individuals. A web-based tool for calculating metaboAge (metaboage.researchlumc.nl) allows easy incorporation in other epidemiological studies. Access to data can be requested at bbmri.nl/samples-images-data.
CONCLUSIONS
In summary, we present a vast resource of metabolomics data and illustrate its merit by constructing a metabolomics-based score for biological age that captures aspects of current and future cardiometabolic health.
Identifiants
pubmed: 33079603
doi: 10.1161/CIRCGEN.119.002610
doi:
Substances chimiques
Biomarkers
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
541-547Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL076200
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA042157
Pays : United States
Organisme : NIMH NIH HHS
ID : RC2 MH089951
Pays : United States