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Metabolomic sweet spot clock predicts mortality and age-related diseases in the Canadian Longitudinal Study on Aging

Abstract:
Background: Chronological age does not capture individual health or resilience. Advances in metabolomics have enabled development of molecular aging biomarkers that capture deviations between biological and chronological age, highlighting how genetics, environment, and lifestyle shape biological aging. Despite their promise, metabolomic biomarkers face challenges such as interpretability, non-linearity, and reproducibility. Methods: We have developed a metabolomic predictor of biological age based on untargeted metabolomic profiling of individuals aged 45–85 years from the Canadian Longitudinal Study on Aging. To enhance interpretability, we first identified metabolites related to health based on variance heterogeneity. For metabolites with identifiable optimal levels, or “sweet spots”, we modeled non-linearity using deviations from these values. A penalized regression model was trained on the Frailty Index using sweet spot deviations as predictors. Results: Here we show that the Sweet Spot Clock built on 178 health-related metabolites is strongly associated with all-cause mortality (HR = 1.08, p = 5.8×1012, C-index=0.841) and age-related diseases. The biomarker outperforms models trained on chronological age and those using raw metabolite levels, underscoring the importance of modeling non-linearity. It remains predictive after adjusting for age, sex, lifestyle and socioeconomic factors, though its added value over standard health and demographic measures is modest. The model generalizes to an independent cohort of individuals aged 85 years and older. Conclusions: The Sweet Spot Clock provides a reproducible and interpretable measure of biological age. By modeling deviations from optimal metabolite levels and training on health status rather than age, it offers a tool for understanding aging heterogeneity and identifying individuals at risk of health decline.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s43856-026-01375-2

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Role:
Author
ORCID:
0000-0002-7707-4740
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Role:
Author
ORCID:
0000-0002-5541-5014
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Role:
Author
ORCID:
0000-0001-9589-2520
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Role:
Author
ORCID:
0000-0002-6674-995X


Publisher:
Nature Research
Journal:
communications medicine More from this journal
Volume:
6
Issue:
1
Pages:
110-110
Publication date:
2026-12-01
DOI:
EISSN:
2730-664X
ISSN:
2730-664X


Language:
English
Keywords:
Pubs id:
2384739
Local pid:
pubs:2384739
Source identifiers:
W7119619557
Deposit date:
2026-03-05
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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