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Aging Cell· 2026Q1

When to Trust Epigenetic Clocks: Avoiding False Positives in Aging Interventions

Daniel S. Borrus, Raghav Sehgal, Judith Armstrong, Jessica Kasamoto et al.

Short summary

New criteria for interpreting epigenetic clock results in anti-aging interventions increase confidence by requiring (1) reliable PC-based clocks to respond, (2) mortality-trained or pace-of-aging clocks to respond, and (3) multiple clocks to respond in the same direction, as demonstrated by simulation and longitudinal data.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Different epigenetic clocks may not agree on the outcome of anti-aging interventions.
  • Three criteria are proposed to increase confidence in epigenetic clock results: reliable PC-based clock response, mortality-trained/pace-of-aging clock response, and consistent direction across multiple clocks.
  • Simulation studies show reliable clocks are more sensitive to true effects.
  • Longitudinal control datasets demonstrate that reliable clock changes are correlated.
  • Some previously published single-clock intervention findings may warrant reexamination.

AI-generated from the title and abstract; the full text is not read.

Abstract

ABSTRACT Epigenetic clocks have emerged as potential biomarkers of aging due to their association with morbidity and mortality. They have recently gained traction as outcome measurements for anti‐aging interventions. However, as the number of new epigenetic clocks continues to grow, different clocks may not agree on the effect of an intervention. This raises the question of when researchers can trust epigenetic clock results. In this study, we find that when extending previously published single‐clock intervention studies to include additional clock models, no additional clocks reach statistical significance. We then analyze clock behavior across positive control datasets (age‐accelerating events) to propose three criteria that increase confidence in a result: (1) reliable PC‐based clocks respond, (2) mortality‐trained or pace‐of‐aging clocks respond, and (3) multiple clocks respond in the same direction. To explain why genuine effects would appear across multiple clocks, we perform a simulation study to demonstrate how reliable clocks are more sensitive to true effects, and use longitudinal control datasets to show that reliable clock changes are correlated with each other. We then show examples of interventions that do satisfy these criteria. These findings provide a framework for interpreting epigenetic clock results in anti‐aging intervention studies, and suggest that some previously published single‐clock findings may warrant reexamination.

The authors' abstract, as published at the source. Aging Cell, 2026 · DOI ↗

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Field: Molecular Biology

Molecular BiologyBiochemistry, Genetics and Molecular Biology