What biomarkers matter most for longevity?
The highest-signal longevity biomarkers cluster across four axes: cardiometabolic (ApoB, Lp(a), triglycerides, HDL, fasting insulin, A1C, HOMA-IR), inflammation (hs-CRP, homocysteine), hormonal (testosterone, estradiol, SHBG, thyroid, DHEA-S), and renal/hepatic context (eGFR, ALT/AST). VO2max and grip strength are non-blood signals worth tracking alongside.
Full answer
Longevity is not predicted by a single biomarker. The highest-signal panel clusters across four axes. Cardiometabolic: ApoB and Lp(a) for atherogenic particle burden, triglycerides and HDL for lipid context, fasting insulin and HOMA-IR for insulin-resistance trajectory, A1C for glycemic average. Inflammation: hs-CRP for systemic inflammation, homocysteine for methylation context. Hormonal: total and free testosterone, estradiol, SHBG, DHEA-S, and a complete thyroid read (TSH, fT3, fT4, reverse T3) because endocrine drift accelerates most aging axes. Renal and hepatic context: eGFR, ALT/AST — these gate which pharmacologic interventions are even available. Non-blood signals matter as much as the labs: VO2max, grip strength, resting heart rate, and HRV consistently track longevity in the literature. The Optimization Blueprint Volume III (The Longevity Code) covers this stack in depth.
Educational. Not a substitute for individualized provider review.
- Biomarkers reference — Primary source · oMeds
- Volume III — The Longevity Code — Reference · oMeds Learn
- Biomarkers explained — Reference · oMeds Learn
- Reviewed by Dr. Laura Purdy, MD, MBA · Clinical Director, oMeds · Last reviewed 2026-05-29

