Cited by 205Metabolomics and Mass Spectrometry StudiesEpigenetics and DNA MethylationGenetics, Aging, and Longevity in Model Organisms

The DOI matches its Crossref record; 88 of the 88 references it cites were found in a registry or an index.

Determinants of accelerated metabolomic and epigenetic aging in a UK cohort

Open access
Robinson, Oliver, Chadeau Hyam, Marc, Karaman, Ibrahim, Climaco Pinto, Rui, Ala-Korpela, Mika, Handakas, Evangelos, Fiorito, Giovanni, Gao, He, Heard, Andy, Jarvelin, Marjo‐Riitta, Lewis, Matthew, Pazoki, Raha, Polidoro, Silvia, Tzoulaki, Ioanna, Wielscher, Matthias, Elliott, Paul, Vineis, Paolo·2020·Aging Cell

Published version of a preprint

Abstract

Markers of biological aging have potential utility in primary care and public health. We developed a model of age based on untargeted metabolic profiling across multiple platforms, including nuclear magnetic resonance spectroscopy and liquid chromatography–mass spectrometry in urine and serum, within a large sample ( N = 2,239) from the UK Airwave cohort. We validated a subset of model predictors in a Finnish cohort including repeat measurements from 2,144 individuals. We investigated the determinants of accelerated aging, including lifestyle and psychological risk factors for premature mortality. The metabolomic age model was well correlated with chronological age (mean r = .86 across independent test sets). Increased metabolomic age acceleration (mAA) was associated after false discovery rate (FDR) correction with overweight/obesity, diabetes, heavy alcohol use and depression. DNA methylation age acceleration measures were uncorrelated with mAA. Increased DNA methylation phenotypic age acceleration ( N = 1,110) was associated after FDR correction with heavy alcohol use, hypertension and low income. In conclusion, metabolomics is a promising approach for the assessment of biological age and appears complementary to established epigenetic clocks.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1111/acel.13149

Cites

88 of 88 references verified0 citation errors · 0 not checkable

Statistics

Figures

FIGURE 1 Summary of metabolomic age prediction. (a) Distribution of Pearson's correlation coefficient (r) between chronological and predicted age across bootstrapped test sets. (b) Metabolomic age plotted against chronological age. (c) Distribution of metabolomic age acceleration scores
FIGURE 1 Summary of metabolomic age prediction. (a) Distribution of Pearson's correlation coefficient (r) between chronological and predicted age across bootstrapped test sets. (b) Metabolomic age plotted against chronological age. (c) Distribution of metabolomic age acceleration scoresCC BY · PubMed Central
FIGURE 2 Metabolomic age plotted against chronological age across different independent study areas. Seven models in this analysis were trained separately on data from participants in six out of the seven study areas and validated with data in the remaining study area shown
FIGURE 2 Metabolomic age plotted against chronological age across different independent study areas. Seven models in this analysis were trained separately on data from participants in six out of the seven study areas and validated with data in the remaining study area shownCC BY · PubMed Central
FIGURE 3 Metabolic network visualisation of significantly enriched pathways based on the manually curated KEGG global metabolic network (Chong et al., 2018). The metabolites of significantly enriched pathways are represented as nodes on the network. Empty nodes represent compounds identified from the feature list by Mummichog but not significant, while solid nodes represent significantly enriched features. Note not all metabolites from the KEGG global network are displayed
FIGURE 3 Metabolic network visualisation of significantly enriched pathways based on the manually curated KEGG global metabolic network (Chong et al., 2018). The metabolites of significantly enriched pathways are represented as nodes on the network. Empty nodes represent compounds identified from the feature list by Mummichog but not significant, while solid nodes represent significantly enriched features. Note not all metabolites from the KEGG global network are displayedCC BY · PubMed Central
FIGURE 4 Associations between risk factors of premature mortality and age acceleration scores. Models adjusted for sex, ethnicity, study centre, income, hypertension, diabetes, BMI, smoking, alcohol intake, physical activity, and fruit, vegetable, meat and fish consumption. Bars show 95% confidence intervals. N (met) and N (epi) columns indicate number analysed for each category for metabolomic age and DNA methylation age measures, respectively
FIGURE 4 Associations between risk factors of premature mortality and age acceleration scores. Models adjusted for sex, ethnicity, study centre, income, hypertension, diabetes, BMI, smoking, alcohol intake, physical activity, and fruit, vegetable, meat and fish consumption. Bars show 95% confidence intervals. N (met) and N (epi) columns indicate number analysed for each category for metabolomic age and DNA methylation age measures, respectivelyCC BY · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 87 references

Research works printed but not linked: 2

  1. 10.1017/S0007125000161896 · DOI · Paper page
  2. World Health Organisation, 2013, Global action plan for the prevention and control of noncommunicable diseases 2013–2020

Cited by

Sorted by citations

See all 205

Metadata

Authors
Robinson, O., Chadeau Hyam, M., Karaman, I., Climaco Pinto, R., Ala-Korpela, M., Handakas, E., Fiorito, G., Gao, H., Heard, A., Jarvelin, M., Lewis, M., Pazoki, R., Polidoro, S., Tzoulaki, I., Wielscher, M., Elliott, P., & Vineis, P.
Affiliations
  • MRC Centre for Environment and Health (GB)
  • MRC Centre for Environment and Health Department of Epidemiology and Biostatistics School of Public Health Imperial College London London UK
  • Computational Medicine, Faculty of Medicine University of Oulu and Biocenter Oulu Oulu Finland
  • University of Sassari (IT)
  • Imperial College London (GB)
  • Italian institute for Genomic Medicine (IT)
Corresponding author
Robinson, Oliver
Venue
Aging Cell
Publisher
Wiley
Published
2020-05-03
Volume
19
Issue
6
Pages
e13149-e13149
ISSN
  • 1474-9718 (ISSN-L)
  • 1474-9726
OpenAlex
W3021249782
Cited by
205
References
87
Citations by year
2026: 42 · 2025: 30 · 2024: 49 · 2023: 33 · 2022: 23 · 2021: 18 · 2020: 9
FWCI
6.70
Type
journal article
Language
en
Open access
Locations
  • Aging Cell (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Brunel University Research Archive (BURA) (Brunel University London) (submittedVersion, cc-by)
  • UnissResearch (Università degli Studi di Sassari) (submittedVersion)
  • Spiral (Imperial College London) (submittedVersion, cc-by)
Funders
Horizon 2020 Framework Programme (633666, 633595, 733206)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolomics and Mass Spectrometry Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
Keywords
biological aging, DNA methylation age, accelerated aging, untargeted metabolomics, lifestyle risk factors, alcohol consumption, depression, obesity, diabetes mellitus, hypertension, socioeconomic status, epigenetic clocks, cross-cohort validation
MeSH terms
Adult, Aged, Aging, Female, United Kingdom, Humans, Male, Middle Aged, Cohort Studies, DNA Methylation, Metabolomics, Young Adult, Epigenomics

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review