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Biological age tests compared: epigenetic clocks, telomeres, blood chemistry and body age apps

Biological age tests compared: epigenetic clocks, telomeres, blood chemistry and body age apps

Specialty Testing Guide › TruAge Biological Age Testing

There are four main ways to put a number on biological age: epigenetic clocks from DNA methylation, telomere length, blood-chemistry scores such as Phenotypic Age, and the "body age" figures shown by apps, smart scales and fitness trackers. They measure different things, and in head-to-head studies they often disagree.

Epigenetic clocks trained on health outcomes and blood-chemistry scores have the strongest research links to disease and death. Telomere length is a weaker marker of aging in people. App-based numbers vary widely, so it is worth asking whether one has ever been tested against health outcomes at all.

Key takeaways

  • Different biological age methods capture different parts of aging, so two methods can give the same person very different results.
  • Health-trained methylation clocks and routine blood-chemistry scores have the best published links with mortality.
  • Telomere length has an inconsistent record as an aging marker in human studies.
  • Consumer "body age" numbers mostly repackage weight, fitness or heart rate data you can already see.

Do these tests measure the same thing?

Not really. One study ran 11 different measures of biological aging, including telomere length, three epigenetic clocks and three blood-and-organ-function composites, in 964 middle-aged people from New Zealand. Contrary to expectation, the measures showed low agreement with each other.1

Some measures did track signs of aging such as physical function, cognitive decline and looking older, but the effect sizes were modest. The authors concluded that the different methods may not be measuring the same aspects of the aging process.1

That is the most important point when comparing tests. A result from one method cannot be checked against a result from another, and switching methods between tests makes any trend meaningless.

Epigenetic clocks

Epigenetic clocks read methylation tags at selected DNA sites, usually from a blood sample, and turn the pattern into an age, a risk score or a speed of aging. The newer clocks, trained on health and survival, are the best-studied methylation tools for predicting disease and death in large groups.

TruDiagnostic's TruAge combines three clocks: OMICmAge for overall biological age, SymphonyAge for 11 organ systems and DunedinPACE for pace of aging. The company itself describes TruAge as not a diagnostic test and positions it as an add-on to a clinical evaluation, not a replacement for standard workup.2

Clocks also carry technical noise. Repeat measurements of the same sample have differed by several years on some older clock versions, which is why small changes between tests deserve caution.3

Telomere length

Telomeres are protective caps on the ends of chromosomes that tend to shorten with age. They sound like an ideal aging marker, but a review of the human evidence concluded that support for telomere length as a biomarker of aging is equivocal.4

A single telomere reading says little on its own about how fast you are aging, and repeat readings can be hard to interpret. The telomere comparison linked below covers why in more depth.

Blood-chemistry age

Phenotypic Age is calculated from chronological age plus 9 routine clinical chemistry markers, the kind already measured in standard blood work. In more than 11,000 US adults, it predicted death from any cause after accounting for age and sex, including among people who seemed healthy.5

The appeal is that its inputs, such as glucose, creatinine, albumin, C-reactive protein and white blood cell counts, are things your clinician already knows how to act on. Its weakness is that those markers can change with a recent illness or a single bad week.

App and device "body age"

Smart scales, fitness watches and online quizzes often report a body age or fitness age. These are usually built from weight, an estimate of body fat, resting heart rate or exercise data. Unless the company has published how the number was built and tested against health outcomes, treat it as a rough summary of inputs you can already see.

MethodWhat it usesStrength of evidence
Epigenetic clocksDNA methylation, usually from bloodStrong population links to disease and death for health-trained clocks; individual noise
Telomere lengthLength of chromosome end capsEquivocal as an aging marker in humans
Blood-chemistry ageAge plus routine lab markersPredicts mortality in large US data; inputs are actionable
App or device body ageWeight, body fat estimate, heart rate, fitnessDepends on the product; look for published testing

Where to go from here

If you are weighing a methylation test against a telomere test, read epigenetic age vs telomere length. If you already have a result from one method and are thinking of switching, remember that the numbers will not line up, so pick one approach and stay with it. For how biological age testing works through our Conshohocken clinic, see the biological age testing hub.

Frequently asked questions

Which biological age test is most accurate?

There is no single winner. Health-trained epigenetic clocks and blood-chemistry scores have the strongest published links to outcomes, but none is a diagnosis, and each has limits for one person.

Can my regular blood work estimate my biological age?

Partly. Phenotypic Age uses routine lab markers, and your clinician can review those markers directly, which is often more useful than a single age figure.

Is a saliva biological age test the same as a blood test?

No. Methylation differs between tissues, so a saliva result and a blood result are not interchangeable. Use the same sample type and method each time if you retest.

Related reading

This article is for general education and is not medical advice. Decisions about testing and treatment should be made with your clinician. If you have severe symptoms, call 911. For a suspected poisoning, call Poison Control at 1-800-222-1222.

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References

  1. Belsky DW, et al. Eleven Telomere, Epigenetic Clock, and Biomarker-Composite Quantifications of Biological Aging: Do They Measure the Same Thing?. Am J Epidemiol 2018. PMID 29149257 · doi:10.1093/aje/kwx346↩
  2. TruDiagnostic. About TruAge. TruDiagnostic 2026. Source↩
  3. Higgins-Chen AT, et al. A computational solution for bolstering reliability of epigenetic clocks: Implications for clinical trials and longitudinal tracking. Nat Aging 2022. PMID 36277076 · doi:10.1038/s43587-022-00248-2↩
  4. Mather KA, et al. Is telomere length a biomarker of aging? A review. J Gerontol A Biol Sci Med Sci 2011. PMID 21030466 · doi:10.1093/gerona/glq180↩
  5. Liu Z, et al. A new aging measure captures morbidity and mortality risk across diverse subpopulations from NHANES IV: A cohort study. PLoS Med 2018. PMID 30596641 · doi:10.1371/journal.pmed.1002718↩
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