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In this interview, Claudia von Boeselager talks with Chris Mirabile about epigenetic clocks and how they are used to assess biological age. They explain that first‑generation clocks (circa 2011) were designed to predict chronological age from DNA methylation patterns, while second‑generation clocks shift focus to biological age, which reflects an individual’s risk of morbidity and mortality. An example of a second‑generation clock is GrimAge, which directly estimates mortality risk. The discussion then moves to the third‑generation Dunedin Pace Clock, developed by researchers at Duke and Columbia and incorporated into Novos’ “Novos Age” product. This clock measures the pace of aging by integrating about 18 biomarkers—including grip strength, brain white‑matter integrity, cognition, sit‑stand performance, and blood markers—derived from a longitudinal study of over 1,000 New Zealanders spanning 50 years. The pace clock is presented as the most sensitive and accurate biological‑age metric, capable of detecting changes within roughly three months. An analogy likens total distance driven over a lifetime to cumulative age, whereas the pace clock reflects current speed, which can be altered quickly. Chris recommends testing once a year to control for seasonal confounders (e.g., sunlight, diet, stress), but suggests quarterly testing for those with no budget constraints who want finer resolution. He emphasizes consistent timing of tests to ensure observed changes are due to interventions rather than seasonal variation. The interview concludes with Claudia inviting viewers to sign up for a short longevity‑and‑lifestyle email newsletter.

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