A Spreadsheet for Calculating Your Levine Phenotypic Age
An excellent paper by M. E. Levine, et al, entitled "An epigenetic biomarker of aging for lifespan and healthspan" describes a technique for combining nine blood-work values with calendar age to calculate your Mortality Score (probability of death in the next ten years) and your Phenotypic Age, i.e., your apparent biological age as implied by your blood variables. The calculation procedure is rather arcane, involving non-obvious unit conversions, exponentials, and logarithms, so I have produced an Excel spreadsheet (LINK) for performing these calculations.
Levine, et al., also used an elaborate DNA analysis of many blood samples to find what they call the DNAm PhenoAge, a measure of the degree of DNA methylation present, a phenomenon associated with aging. They correlate this measure with the Phenotypic Age, showing that they track very well. My spreadsheet uses a fit to their plots to estimate your DNAm PhenoAge and the modified Mortality Score that it implies.
You may already have blood-work giving the nine blood variables needed to use this spreadsheet, but if not they can be obtained by purchasing the blood-work of LifeExtension's Chemistry Panel & Complete Blood Count (CBC) ($35) and their C-Reactive Protein (CRP), Cardiac ($42). On the spreadsheet at the upper line of blue numbers, you simply enter your values in place of the ones presently there and enter your decimal calendar age in the last column. The calculated results then appear in red on the last line.
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You may find this online tool useful. https://agingmetrics.org/CalculatePhenAgeResp.aspx
Enter Levine/Horvath markers directly and calculate - or extract values if lab reports are from Life Extension (run by LabCorp). And most recent ones directly from LabCorp will extract. Lab reports scanned to PDF do not actually contain the data and will not work.
Useful info: https://agingmetrics.org/CalculatePhenotypicAge.html
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After months of research, I finally got my bloods done and used the spreadsheet shared above. However, I have thalassemia minor (no physiological symptoms and my iron panel is good) however, since I have small RBC, my RCDW is large (18) vs. normal range of 10 to 15. This increases my estimated age by nearly 35% (c. 48 vs actual age of 36). Ceteris paribus, if my RCDW was 10 to 15, my phenotypic age would be between 18 and 37 (mid. = 28)
I have also run my number through aging.ai (3.0) which doesn't use RCDW and my phenotypic age is between 20 and 41 depending on selected ethnicity. I get 20 - 22 when ethnicity is Europe, Asia (ex. Middle East) and America (excluding Central and South America). Otherwise, for ME, South/Central America and Africa, I am phenotypically 41. Is there a racial bias or are insufficient data points for Africa, South America, Middle East and Oceania?
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Bill Faloon is also using Levine's Phenotypic Age to calculate his biological age. See his new post: https://age-reversal.net/wp-content/uploads/2023/08/2023.07.17-Bill-Faloon-Biological-Age-Blood-Test-Panel.pdf
I am also happy I was the one who spot with authors (Zuyun Liu) the mistake in the formula which was corrected in the paper correction of 2019. I was using my own spread sheet before JGC published his super elegant version. Note also the he made (as described above) a calculation to estimate Levine's PhenoAge which requires methylation data.
BTW, I am also ~15 years "younger" than my age at the same Faloon's (chrono) age ... ;-)
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Two interesting studies from the same Swedish team using a similar data set using Levine's PhenotypicAge and PhenoAge and comparison with different BA measurement methodologies.
Mak JKL, McMurran CE, Kuja-Halkola R, et al. Clinical biomarker-based biological aging and risk of cancer in the UK Biobank. Br J Cancer. 2023;129(1):94-103.
Mak JKL, McMurran CE, Hägg S. Clinical biomarker-based biological ageing and future risk of neurological disorders in the UK Biobank. J Neurol Neurosurg Psychiatry. Published online October 26, 2023.