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Longevity Score

See whether your routine blood markers line up with healthier aging patterns before any one result looks clearly off.
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Tested by Quest or Access Medical
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Explained with clear next steps, no medical jargon

Should you take a Longevity Score test?

This test is most useful if any of these apply to you.

Healthy but Want to Stay Ahead
You feel fine and want to see whether your blood-marker pattern lines up with healthier aging.
Changing Diet and Training
You're changing how you eat, move, or sleep and want to see whether the blood-marker pattern shifts.
Worried About Family Heart Risk
Early heart disease or diabetes runs in your family, and you want a broader blood-marker baseline.
Tracking a Longevity Protocol
You're using a protocol aimed at aging and want to track the component markers behind the score.

About Longevity Score

Two people can be the same age on the calendar and have very different blood-marker patterns. Yearly bloodwork can hold clues, but most labs are read one number at a time. This score combines routine blood markers into a single estimate of whether your biology looks more like a healthier-aging pattern or a higher-risk one.

This is a newer, exploratory aging measure. It is not a diagnosis, and there is no official cutoff. Use it as a baseline and a trend, then read the score beside the markers that created it.

What the Score Actually Measures

The Longevity Score is not one substance in your blood. The specimen is a blood draw. Some inputs are measured from serum or plasma and others from whole blood, but the score itself is calculated after the component tests are done.

The score is built from many routine markers at once, weighting patterns linked with healthier aging. Inflammation, blood sugar control, cholesterol handling, immune balance, kidney function, and liver function can all affect it.

Published models like this use machine learning trained on large medical-record datasets. In one Nature Aging model, a mildly low neutrophil count and lower alkaline phosphatase tracked with healthier aging apart from major chronic disease risk. Neutrophils are a type of white blood cell. Alkaline phosphatase is an enzyme measured in routine blood chemistry. Those patterns would be easy to miss if each marker were read alone.

Because the inputs are ordinary blood tests, the score measures your marker profile directly. What it reflects, aging speed, is an inference drawn from how those markers behave in large populations, not something the blood literally shows.

What Accelerated Aging Tracks With

The strongest outcome data come from related biological-aging scores, not this exact Longevity Score. In a UK Biobank cohort of 332,012 adults, people in the fastest-aging quarter had 54% higher overall mortality risk and 41 to 44% higher risk of developing more than one chronic condition than those in the slowest-aging quarter.

Life expectancy moved the same way. At age 45, people who already had three overlapping condition categories lost 5.3 years compared with healthy peers. If their biological aging was also accelerated, the loss was another 5.8 to 7.0 years in that study. These figures came from KDM-BA and PhenoAge, not this score.

Related composite health scores point the same way. Adults with the healthiest profiles on a widely studied heart-health index lived longer free of heart disease, diabetes, cancer, and dementia: roughly 6.9 more disease-free years for men and 9.4 for women, measured from age 50. That index is not this score, but it is built from overlapping ingredients.

A low Longevity Score is a prompt to look closer, not a verdict. Its main use is pattern recognition: it can flag a set of ordinary-looking labs that may deserve attention together.

Why One Reading Is Not Enough

This score has no official cutoff that says healthy above here, worried below there. That sounds like a weakness. It is why your trend matters more than any single number: your own past readings become the reference point that no population range can give you.

One reading can wobble after a cold, surgery, or a hard race. A repeated direction is harder to fake, especially when the same component markers explain it each time.

Why a Single Reading Can Fool You

A few things can push the number around without your aging actually changing. The first one matters most, because it is common and easy to miss.

  • Recent illness or surgery: inflammation markers can stay high for days to weeks after an infection or operation, which can pull the score down during recovery.
  • A hard workout in the last few days: long races and hard training can temporarily raise inflammation and muscle markers, so a rested draw is cleaner.
  • Anti-inflammatory medications: statins, GLP-1 drugs, and metformin can lower C-reactive protein or other inflammatory markers. That may improve the score before anyone knows whether aging itself changed.
  • Steroids: corticosteroids can raise blood sugar and shift white blood cell counts within hours, so a result during a short course may not be your baseline.

What Moves This Biomarker

Evidence-backed interventions that affect your Longevity Score level

↑ Increase
Follow supervised long-term calorie restriction without nutrient shortfall
A two-year trial assigned healthy adults without obesity to cut calorie intake by 25%; on average they achieved about a 12% cut. Their DunedinPACE score, a DNA-based pace-of-aging clock, slowed by about 2 to 3%. This did not directly test the Longevity Score, so it is evidence from another aging measure.
DietModest Evidence
↑ Increase
Do structured exercise for at least 16 weeks
A meta-analysis of randomized trials found structured exercise helped maintain telomere length and raised telomerase activity. Telomeres are protective caps on chromosomes. Telomerase helps maintain them. These were cellular aging markers, not this blood-marker score, so this supports plausibility rather than a measured score change.
ExerciseModest Evidence
↑ Increase
Follow a Mediterranean-style eating pattern
In 4,510 Italian adults, closer adherence to a Mediterranean diet was linked with less biological-age acceleration on a 36-blood-marker aging index. That index was not this exact score, and the study was cross-sectional, so it cannot prove the diet caused the shift.
DietModest Evidence
↑ Increase
Raise overall diet quality across the board
In 2,694 women, higher diet quality was linked with younger readings on DNA-based aging clocks, especially PhenoAge and GrimAge. The study used whole-blood DNA data, not this Longevity Score, and shows correlation only.
DietModest Evidence
↑ Increase
Take a GLP-1 receptor agonist (such as semaglutide or liraglutide)
Across 52 randomized trials in type 2 diabetes, GLP-1 receptor agonists lowered C-reactive protein and several related inflammatory markers compared with placebo or other diabetes therapies. Because inflammation markers can feed this score, the score may rise. No trial has shown that these drugs improve this exact Longevity Score or slow aging by this measure.
MedicationModest Evidence

Frequently Asked Questions