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Biomarkers

Biological Age Calculator: Levine Phenotypic Age from Bloodwork

Free biological age calculator. Computes Levine phenotypic age from 9 blood markers plus chronological age, per Levine 2018, JAMA Network Open.

Parameters

Phenotypic age

- yr

Chronological

- yr

Delta

-

10-yr mortality risk

- %

- / 9 markers in longevity-optimal range.

Coefficients from Levine et al. 2018. Reported as a scalar; interpret in context of other inputs and clinician judgment. Not a diagnostic tool. This is an editorial estimate based on published research, not a medical test result. Out-of-range values warrant clinical follow-up, not self-treatment.

Editorial reference

Optimal vs lab-reference ranges

These are editorial reference points, not clinical targets. Discuss any out-of-range value with a clinician. The "optimal" band is what the longevity literature associates with the lowest all-cause mortality, not what your lab will tell you to chase.

  • hs-CRP

    mg/L
    Lab
    Optimal
    less than 3
    less than 0.5

    Acute inflammation distorts a single reading. Repeat after 6 weeks if elevated.

  • HbA1c

    %
    Lab
    Optimal
    less than 5.7
    4.8 to 5.2

    Reflects 2 to 3 month glycaemia. Anaemia and haemoglobin variants can bias the reading.

  • Lp(a)

    mg/dL
    Lab
    Optimal
    less than 50, or less than 125 nmol/L
    less than 30

    Largely genetic. Measure once in adulthood; repeat only on major intervention.

  • Fasting insulin

    uIU/mL
    Lab
    Optimal
    2 to 24
    less than 5

    Lab "normal" runs much wider than the longevity-optimal band. Pair with fasting glucose for HOMA-IR.

  • Albumin

    g/dL
    Lab
    Optimal
    3.5 to 5.0
    4.3 to 5.0

    Low-normal albumin tracks all-cause mortality even within the lab reference range.

  • DHEA-S

    ug/dL
    Lab
    Optimal
    80 to 560 (adult)
    age and sex percentile

    No single optimal number. Target the 75th percentile for your age and sex; absolute cutoffs are misleading.

  • Telomere length

    kb
    Lab
    Optimal
    lab-specific
    measurement is brittle

    Inter-lab variability is large; intra-individual variation between draws is also large. Treat trends with skepticism, not single readings.

Optimal bands derive from observational cohorts (Framingham, ARIC, NHANES) and longevity-clinic consensus, not from regulatory cutoffs. They reflect where mortality curves bottom out, which is a different question from what triggers a clinical diagnosis. A lab "normal" can mask a 10 to 20 year horizon risk; a lab "abnormal" can be benign in context.