The thing everyone talks about and almost nobody measures directly. Every method in use is an approximation of one nobody can have.
Insulin resistance is the state where your tissues respond less to insulin, so the pancreas makes more of it to get the same effect. For years before blood sugar rises at all, insulin can be climbing to hold it down. That is why someone can have a normal glucose and still be well down a metabolic road.
Measuring it properly is another matter.
The hyperinsulinaemic‑euglycaemic clamp is the reference method. Insulin is infused at a fixed rate while glucose is infused at whatever rate keeps blood sugar steady; how much glucose it takes tells you how well insulin is working. It takes hours, needs two lines and constant monitoring, and exists in research units.
Every other method is an approximation of it, and should be read as one.
HOMA‑IR is calculated from a fasting glucose and a fasting insulin drawn at the same moment. The arithmetic differs by units — with glucose in mg/dL it is glucose × insulin ÷ 405; in mmol/L it is glucose × insulin ÷ 22.5.
Its weaknesses are worth knowing before you pay for it:
It is still useful, particularly repeated in the same laboratory over time, where the direction of travel matters more than the absolute figure.
Two things already on an ordinary panel carry information about insulin resistance and cost nothing extra:
Neither is a measurement of insulin resistance. Both are signals that it is likely, which is usually what a clinician actually needs.
Fasting insulin is an immunoassay and costs around ₡18,000 — more than twice a fasting glucose. We left it out of the baseline deliberately, and the question that settled it was: would the result change what we do next?
For most people arriving with fatigue and stalled weight, it would not. Glucose, HbA1c, triglycerides and HDL between them already say whether the metabolic picture is worrying, and the next step is the same either way.
Where it does change a decision — a normal HbA1c with a strong family history, or a picture that does not add up — it goes on as an addition. That is what the per‑treatment list is for.
Insulin resistance is not one thing. The liver, muscle and fat can be resistant to different degrees in the same person, and no blood test on this page separates them. Published thresholds also come largely from European and North American cohorts, and how well they transfer to a Costa Rican population is not something we can answer from the literature we have read.
What it means for you depends on the rest of your results and your history, which is a conversation with a physician rather than a calculation.
Every patient starts the same way: thirty minutes with a physician, then a full biomarker panel drawn at a laboratory near you. Whether any medicine follows is your doctor’s decision, made after reading your results with you.
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