Longevity

What becomes readable

A magnetic sensor built by your own cells, read by a coil. Whether a marker works comes down to one thing — how many molecules of it are actually floating in your blood.

Readable At the edge Out of reach for now

Physical signals

no chemistry needed

The magnets ride in your blood, so every heartbeat sweeps a surge of them past the coil. These come free with the signal.

Heart rate Signal swells once per beat Free
Pulse waveform Shape of each beat, not just the rate Free
Heart rate variability Beat-to-beat timing Free
Core body temperature Magnetic response shifts with temperature Free
Blood pressure Via pulse timing between two points Plausible

Abundant

millimolar — millions of molecules per sensor

Enormous headroom. These are the easy wins and they'd work first.

Glucose 4–6 mM Yes
Lactate 0.5–2 mM at rest, up to 20 mM working Yes
Ketones 0.1–3 mM Yes
Alcohol mM while drinking Yes
Sodium & hydration 135–145 mM Yes
Urea (kidney) 2.5–7 mM Yes
Calcium 2.2–2.6 mM Yes
Magnesium 0.7–1 mM Yes
Uric acid 200–400 µM Yes
Creatinine (kidney) 60–110 µM Yes

Reachable

nanomolar — above the 1 nM detection floor

This is the interesting tier. Nothing on the market gives you any of these continuously.

Cortisol the prize 100–500 nM · the actual stress hormone, not inferred Yes
CRP — inflammation the surprise 9–26 nM normal · up to 900 nM when sick Yes
Vitamin D 50–125 nM Yes
Testosterone 10–35 nM Yes
Melatonin ~0.3 nM at night peak — right at the floor Edge

Out of reach

picomolar — too rare to clump a sensor

Fewer than one molecule per sensor. Nothing to grab onto. These need a further invention — see below.

Insulin 20–200 pM No
Estradiol 100–1500 pM No
Thyroid (TSH, free T4) 1–25 pM No
IL-6, TNF-α ~0.05–0.5 pM No
Ferritin 44–660 pM No

Sleep isn't one measurement

There's no accelerometer, so there's no movement data. But you get the four signals a watch uses to guess at sleep — measured instead of inferred.

What would unlock the bottom tier

One trick: catalytic amplification — make a single analyte molecule trigger many sensors instead of one, the way one enzyme chews through thousands of substrates.

That's what moves insulin, thyroid and the cytokines from out of reach to abundant. Nobody is currently doing it in the magnetic domain. It's the single highest-value open problem here.