Audited ·Last updated 29 Jul 2026·6 citations·Tier 1·0 uses

HOMA-IR Calculator

Calculate HOMA1-IR and HOMA1-%S from fasting glucose and insulin. HOMA is assay-dependent: there is no universal normal, so compare with your own lab.

HOMA-IR Calculator

After 8+ hours without food
Glucose unit
µU/mL, also written mIU/L — not pmol/L
No universal value exists — use your own lab's
HOMA1-IR
1.7762
HOMA values depend on the insulin assay used. There is no universal normal — compare with your own laboratory's reference range.
HOMA1-%S (sensitivity)
56.2988%
Fasting glucose (mmol/L)
4.9957
Fasting glucose (mg/dL)
90
Your cut-off
2.05
Margin to your cut-off
-0.2738
Vs your cut-off
Below your cut-off

Background.

HOMA-IR is a way of turning two ordinary fasting blood results — glucose and insulin — into a single number that describes how hard the pancreas is working to hold that glucose down. It comes from the homeostasis model assessment published by David Matthews and colleagues at Oxford in Diabetologia in 1985. Their insight was that fasting glucose and fasting insulin are not two independent facts about a person; they are the resting equilibrium of a feedback loop, and where that equilibrium sits tells you something about how sensitive the tissues are to insulin. The linear approximation the paper gave is startlingly simple: multiply fasting insulin in µU/mL by fasting glucose in mmol/L and divide by 22.5. Someone with textbook-normal values of 5 µU/mL and 4.5 mmol/L lands on exactly 1.0, which is where the 22.5 comes from.

Before the number is worth anything, one thing has to be said clearly, because it changes how every HOMA-IR result should be read: there is no universal normal value. This is not a hedge invented for a web page. It is the position of the Oxford Diabetes Trials Unit, the group that owns and licenses HOMA, stated on their own site: 'There is no absolute value for HOMA indices. These will depend on the specific assays used for glucose, insulin and C-peptide. Because of this, there are no defined thresholds for normal vs. abnormal values.' Insulin immunoassays are notoriously non-interchangeable — they cross-react differently with proinsulin and its split products and are calibrated against different standards — so the same serum sent to two laboratories can produce HOMA-IR values that differ by more than the gap between the thresholds people argue about. That is why this calculator makes the comparison threshold an input you fill in rather than a constant it decides for you.

The field default of 2.05 is a real, named, dated number and not a consensus. It is the optimal cut-off for non-diabetic men under IDF metabolic-syndrome criteria in the EPIRCE study, a random sample of 2,459 Spanish adults. That same study found 1.85 for men under ATPIII criteria, and for non-diabetic women a cut-off that moved with age — 2.31 at age 30, 2.07 at age 50, 2.47 at age 70 — while a 90th-percentile criterion put the threshold at 3.46. The authors noted that all their values sat between the 70th and 75th percentiles of the Spanish adult distribution, and that cut-offs 'are different according to ethnicity, clinical methods of estimation, and metabolic conditions'. Replace the default with whatever your own laboratory or study protocol uses. If you have no such number, treat the comparison as decorative and use the HOMA-IR value itself for tracking change over time, which is what it is genuinely good for.

Precision is the second thing to know. The original paper reported that its insulin-resistance estimate correlated with the euglycaemic clamp at Rs = 0.88, which is impressive for two fasting tubes of blood, but the same authors wrote in the same abstract that 'the low precision of the estimates from the model (coefficients of variation: 31% for insulin resistance and 32% for beta-cell deficit) limits its use'. A coefficient of variation of 31% means a single HOMA-IR of 2.4 is entirely compatible with a true value near 1.7 or near 3.1. Small differences between two measurements, and small margins to a threshold, are noise. Differences of a factor of two, sustained across repeated tests, are signal.

This page computes HOMA1, the 1985 linear approximation, not HOMA2. Oxford's HOMA2 is an iterative computer model published in 1998 that simulates the underlying physiology rather than approximating it, and it accounts for variation in hepatic and peripheral glucose resistance, renal glucose loss and the proinsulin content of insulin assays. Oxford themselves describe the HOMA1 formulae as providing 'only linear approximations'. HOMA1 and HOMA2 do not produce the same numbers, and a value from one cannot be compared with a threshold from the other. If you are reading a paper, check which it used before comparing your result to it.

There is a small arithmetic point that is worth being explicit about, because it will make this calculator disagree very slightly with most others. The model is defined in mmol/L. The mg/dL version everyone quotes divides by 405, which is exactly 22.5 × 18 — it embeds a glucose conversion factor rounded from 18.0156 down to 18. This calculator converts with the exact factor derived from the molar mass of glucose (C₆H₁₂O₆ = 180.156 g/mol, from IUPAC's 2023 abridged standard atomic weights) and then divides by 22.5. At the values this page loads with, 90 mg/dL and 8 µU/mL, the exact route gives 1.7762 and the 405 route gives 1.7778 — a difference of 0.087%, roughly three hundred times smaller than the model's own 31% coefficient of variation. It is disclosed rather than hidden, but it should never change a decision.

Two things are deliberately missing. First, there is no pmol/L option for insulin. The conversion between µU/mL and pmol/L depends on which insulin standard the assay is calibrated against, and different reference preparations give materially different factors; rather than pick one and bake it in, this page asks for µU/mL (equivalently mIU/L) and tells you to get that figure from your laboratory. Second, HOMA-%B, the beta-cell function companion index, is not computed. Its linear approximation is widely quoted, but I could not retrieve it from a primary source — the Diabetologia and Diabetes Care full texts are both behind access controls and Oxford's public FAQ gives the equation for insulin resistance only. A clinical constant that cannot be verified does not get shipped, so the page is narrower and honest rather than complete and guessed.

Finally, a boundary of applicability that follows from the model itself. Matthews and colleagues opened by saying that 'the steady-state basal plasma glucose and insulin concentrations are determined by their interaction in a feedback loop'. The loop is between glucose and the pancreas's own insulin output. If the fasting insulin in your blood arrived from a syringe rather than from your beta cells, that loop is not the thing being measured and HOMA-IR does not describe what it claims to describe. The same caution applies to anyone whose insulin assay may be cross-reacting with an insulin analogue. HOMA-IR is a research and epidemiology instrument used in enormous numbers of studies; it is not a diagnostic test, and no clinical decision should rest on it alone.

What is homa-ir calculator?

The homeostasis model assessment is a mathematical description of the resting relationship between blood glucose and blood insulin. In a person whose tissues respond normally to insulin, a modest amount of insulin holds fasting glucose in the normal range. As tissues become less responsive, the pancreas compensates by secreting more insulin, so fasting insulin rises while glucose stays normal for a time — and it is that combination, normal glucose bought with high insulin, that HOMA-IR is designed to detect. HOMA1-IR is the linear approximation to the full model: fasting insulin in µU/mL multiplied by fasting glucose in mmol/L, divided by 22.5. The divisor normalises the index so that a healthy reference individual scores 1.

HOMA1-%S is the same information turned inside out. Oxford describe HOMA-IR as the inverse of HOMA-%S, and %S is expressed as a percentage of a normal reference population, so %S is simply 100 divided by HOMA-IR. A HOMA-IR of 2 corresponds to 50% sensitivity; a HOMA-IR of 4 to 25%. Because it is an exact reciprocal it adds no information, and this page shows it only because a large part of the literature reports sensitivity rather than resistance and readers need to be able to move between the two. Neither index is a diagnosis. Both describe a fasting equilibrium at one moment, measured with an assay whose calibration is not standardised between laboratories.

How to use this calculator.

  1. Use a fasting sample — at least eight hours without caloric intake, and both tubes drawn at the same time. Glucose and insulin from different visits do not describe one equilibrium.
  2. Enter fasting plasma glucose and choose its unit. mg/dL is usual in the United States and Japan; mmol/L almost everywhere else.
  3. Enter fasting insulin in µU/mL, which your laboratory may print as mIU/L — the two are the same. If your report shows pmol/L, ask the laboratory for the µU/mL figure rather than converting it yourself: the factor depends on the assay's calibration standard.
  4. Replace the reference cut-off with the threshold your own laboratory, clinician or study protocol uses. The default of 2.05 is one population's value, not a standard.
  5. Read HOMA1-IR alongside the margin to your cut-off, and remember the model's 31% coefficient of variation before treating a small margin as meaningful.
  6. If you are comparing against a published paper, check whether it used HOMA1 or HOMA2, and which insulin assay. Values from different models and different assays are not interchangeable.
  7. Take the result to a clinician. HOMA-IR is a research and epidemiology instrument, not a diagnostic test.

The formula.

HOMA1-IR = ( I₀ × G₀ ) ⁄ 22.5

The equation is one multiplication and one division. Fasting insulin in µU/mL is multiplied by fasting glucose in mmol/L, and the product is divided by 22.5. Oxford's Diabetes Trials Unit states it as 'HOMA1_IR = (FPI x FPG)/22.5', and the EPIRCE investigators state it independently as 'fasting serum insulin (µU/ml) × fasting plasma glucose (mmol l⁻¹)/22.5' — two sources, identical equation, identical units. The constant 22.5 is the product of a reference fasting insulin of 5 µU/mL and a reference fasting glucose of 4.5 mmol/L, which is what makes a healthy reference individual score 1.0 rather than some arbitrary number.

When the input is in mg/dL it has to be converted first, and the conversion is where this calculator diverges very slightly from convention. The universally quoted mg/dL form divides by 405, and 405 is exactly 22.5 × 18 — so using it is identical to converting glucose with a factor of 18 rather than 18.0156. This page converts with 18.0156, derived from the molar mass of glucose: IUPAC's 2023 abridged standard atomic weights give C = 12.011, H = 1.0080 and O = 15.999, so C₆H₁₂O₆ = 6(12.011) + 12(1.0080) + 6(15.999) = 180.156 g/mol, and one mmol/L of glucose is 18.0156 mg/dL. Working the shipped defaults both ways: 90 mg/dL ÷ 18.0156 = 4.99567 mmol/L, so HOMA1-IR = 8 × 4.99567 ÷ 22.5 = 1.7762, whereas 8 × 90 ÷ 405 = 1.7778. The gap is 0.087%. It is disclosed because a reader comparing two calculators deserves to know why the last digits differ, not because it matters clinically.

Rounding happens at one place only: the return boundary. The unit conversion, the product, the division by 22.5 and the reciprocal for HOMA1-%S are all carried at full decimal precision, and each output is rounded once, at the end, to ten decimal places. In particular, the comparison against your cut-off is made on the unrounded value, so a HOMA1-IR that lands exactly on the threshold reports 'at or above' with no rounding ambiguity — the shipped test suite asserts this at exactly 2.0, and immediately either side of it.

HOMA1-%S is the exact reciprocal, scaled: 100 ÷ HOMA1-IR. Because both inputs are guarded to be strictly positive, HOMA1-IR is strictly positive and the reciprocal can never divide by zero. The relationship is inverse and non-linear, which is worth internalising: moving from a HOMA1-IR of 1 to 2 halves %S from 100% to 50%, but moving from 4 to 5 takes it only from 25% to 20%. Equal steps in resistance are not equal steps in sensitivity, and papers that report one can look very different from papers that report the other while describing identical data.

A worked example.

Example

A fasting panel returns glucose 5.6 mmol/L and insulin 15 µU/mL. Because the glucose is already in the unit the model uses, no conversion is needed: HOMA1-IR = 15 × 5.6 ÷ 22.5 = 84 ÷ 22.5 = 3.7333. For readers working in conventional units, the same glucose is 5.6 × 18.0156 = 100.89 mg/dL. HOMA1-%S is 100 ÷ 3.7333 = 26.79%, meaning this equilibrium sits at roughly a quarter of the model's reference sensitivity. Against the default cut-off of 2.05 the margin is 3.7333 − 2.05 = +1.6833, so the result is at or above that threshold. Note what this does and does not say. The glucose is unremarkable — 5.6 mmol/L is below the 7.0 mmol/L diabetes threshold and below the 6.1 mmol/L impaired-fasting-glucose line — and it is the insulin that is doing the work, which is exactly the pattern HOMA-IR exists to surface. But 2.05 is one Spanish study's cut-off for non-diabetic men, this laboratory's insulin assay may not be the one that study used, and the model's own coefficient of variation is 31%, so a repeat measurement of 2.8 or 4.9 would be entirely consistent with these numbers. The defensible reading is 'high enough to be worth a conversation and worth repeating', not 'insulin resistant'.

glucose Unitmmol/L
reference Cutoff2.05
fasting Insulin15
fasting Glucose5.6

Frequently asked questions.

What counts as a normal HOMA-IR?
There is no answer to this that holds everywhere, and the group that owns HOMA says so directly. Oxford's Diabetes Trials Unit states that 'There is no absolute value for HOMA indices. These will depend on the specific assays used for glucose, insulin and C-peptide. Because of this, there are no defined thresholds for normal vs. abnormal values.' Insulin immunoassays cross-react differently with proinsulin and are calibrated against different standards, so the same sample can yield materially different HOMA-IR values in different laboratories. Published population cut-offs exist — the EPIRCE study of 2,459 Spanish adults reported 1.85 and 2.05 for non-diabetic men under two different metabolic-syndrome definitions, age-varying values of 2.07 to 2.47 for women, and 3.46 on a 90th-percentile criterion — but they are that population, that assay and that criterion. Use your own laboratory's range if it has one.
Why is the cut-off an input on this page instead of built in?
Because baking one in would be inventing a clinical constant that the instrument's own custodians say does not exist. Every calculator that prints 'normal' or 'insulin resistant' beside a HOMA-IR has quietly chosen a threshold from one study in one population measured on one assay, and has hidden that choice from you. Making it an editable field with a named, dated default does the opposite: you can see which number the comparison uses, you can see where it came from, and you can replace it with the one your clinician or protocol actually uses. If you have no threshold to hand, ignore the comparison entirely and use the HOMA-IR value for tracking change over time in the same laboratory, which is far more robust than any single cross-sectional cut-off.
What is the difference between HOMA1 and HOMA2?
HOMA1 is the 1985 linear approximation — the (insulin × glucose)/22.5 arithmetic this page computes. HOMA2 is a later iterative computer model from the same Oxford group that simulates the underlying physiology instead of approximating it, accounting for variation in hepatic and peripheral glucose resistance, renal glucose loss and the proinsulin content of insulin assays. Oxford describe the HOMA1 formulae as providing 'only linear approximations' and distribute a separate HOMA2 calculator. The two do not produce interchangeable numbers, so a HOMA1 value cannot be compared against a HOMA2 threshold or vice versa. If you are comparing your result with a published study, check which model that study used before drawing any conclusion.
Why divide by 22.5 instead of 405?
They are the same operation applied to different units, and 405 involves a small rounding this page avoids. The model is defined with glucose in mmol/L and divides by 22.5, which is 5 µU/mL × 4.5 mmol/L — the reference pair that makes a healthy individual score 1.0. The mg/dL shortcut divides by 405, and 405 is exactly 22.5 × 18, which means it converts glucose with a factor of 18 rather than the true 18.0156 implied by glucose's molar mass of 180.156 g/mol. This calculator converts with 18.0156 and then divides by 22.5. At the default values of 90 mg/dL and 8 µU/mL the two routes give 1.7762 and 1.7778 — 0.087% apart. That is about three hundred times smaller than the model's own 31% coefficient of variation, so it never changes an interpretation, but it explains any tiny disagreement with another tool.
My laboratory reports insulin in pmol/L. What do I do?
Ask the laboratory for the µU/mL (mIU/L) figure, or for their own conversion factor, rather than converting it yourself from a factor found online. The relationship between µU/mL and pmol/L depends on which international insulin standard the assay is calibrated against, and the commonly circulated factors are not all derived from the same reference preparation. This page deliberately does not offer a pmol/L input for exactly that reason: it would mean choosing one factor and presenting it as if it were universal. Since HOMA-IR is already assay-dependent, adding an assay-dependent unit conversion on top would compound an uncertainty the user cannot see.
Why doesn't this page show HOMA-%B for beta-cell function?
Because the equation could not be verified against a primary source. HOMA-%B is the companion index from the same 1985 paper, and its linear approximation is widely reproduced, but the Diabetologia full text and the Diabetes Care review that discusses it are both behind access controls, and Oxford's public FAQ gives the equation for insulin resistance only. This project's rules forbid shipping a clinical constant that cannot be traced to a primary source, so the index is omitted and the omission is stated rather than quietly filled in from memory. The approximation is also singular at a fasting glucose of 3.5 mmol/L, which would have needed a domain guard that no retrievable source justifies.
How accurate is HOMA-IR compared with a glucose clamp?
Good at the group level, coarse at the individual level. The original paper reported that its insulin-resistance estimate correlated with the euglycaemic clamp at Rs = 0.88 (p < 0.0001), which is remarkable for two fasting tubes of blood against a multi-hour laboratory procedure. But the same abstract states that 'the low precision of the estimates from the model (coefficients of variation: 31% for insulin resistance and 32% for beta-cell deficit) limits its use'. A 31% coefficient of variation means a single measured HOMA-IR of 2.4 is compatible with a true value anywhere from roughly 1.7 to 3.1. That precision is fine for comparing groups of hundreds in an epidemiological study, and poor for deciding anything about one person from one blood draw.
Can I use HOMA-IR if I take insulin?
No, and the reason is structural rather than a matter of degree. Matthews and colleagues built the model on the premise that 'the steady-state basal plasma glucose and insulin concentrations are determined by their interaction in a feedback loop' — a loop between circulating glucose and the pancreas's own secretion. If the insulin in a fasting sample arrived from an injection, that loop is not what is being measured, and the resulting number does not mean what the index claims to mean. The same caution applies where an insulin immunoassay may cross-react with an insulin analogue. HOMA-IR is used in people with type 2 diabetes not on insulin and in non-diabetic populations; for insulin-treated patients it is not the right instrument.
What is HOMA1-%S and why show it as well?
It is insulin sensitivity expressed as a percentage of the model's normal reference population, and it is exactly the reciprocal of HOMA-IR: Oxford describe HOMA-IR as 'the inverse of HOMA_%S', so %S = 100 ÷ HOMA-IR. A HOMA-IR of 2 is 50% sensitivity, 4 is 25%, 5 is 20%. It carries no information the IR value does not, and it is shown here purely so readers can move between papers, because a large part of the literature reports sensitivity rather than resistance. The inverse relationship is worth internalising: equal increments in resistance are not equal decrements in sensitivity, so a plot of %S compresses everything at the resistant end of the range.
Does a high HOMA-IR mean I have diabetes or prediabetes?
No. Diabetes and prediabetes are defined by glucose and HbA1c thresholds, not by HOMA-IR, and HOMA-IR is not part of any diagnostic criterion. What it can do is describe a pattern that glucose alone hides: a fasting glucose sitting comfortably in the normal range while fasting insulin is high is exactly the compensated state HOMA-IR was built to surface, and it can be present for years before glucose starts to drift. That makes the index interesting for research and for tracking, and it does not make it a test. Interpret a high value as a reason to talk to a clinician about your whole metabolic picture, and to repeat the measurement, rather than as a result in itself.

References& sources.

  1. [1]Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. "Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man." Diabetologia. 1985;28(7):412-419. doi:10.1007/BF00280883. Original model. Source of the feedback-loop premise, the clamp correlation Rs = 0.88, and the authors' own precision caveat (coefficients of variation 31% for insulin resistance and 32% for beta-cell deficit). Abstract open on PubMed (PMID 3899825); full text paywalled. Retrieved 29 July 2026.
  2. [2]University of Oxford, Radcliffe Department of Medicine, Diabetes Trials Unit. "HOMA — Frequently Asked Questions." The custodians of HOMA. Source of the equation 'HOMA1_IR = (FPI x FPG)/22.5', of the statement that HOMA1 formulae provide 'only linear approximations of HOMA_%B and HOMA_IR, the inverse of HOMA_%S', and of the key scope limit: 'There is no absolute value for HOMA indices. These will depend on the specific assays used for glucose, insulin and C-peptide. Because of this, there are no defined thresholds for normal vs. abnormal values.' Retrieved 29 July 2026.
  3. [3]University of Oxford, Radcliffe Department of Medicine, Diabetes Trials Unit. "HOMA Calculator" overview page: "The Homeostasis Model Assessment (HOMA) estimates steady state beta cell function (%B) and insulin sensitivity (%S), as percentages of a normal reference population." Source of the definition of %S as a percentage of a normal reference population. Retrieved 29 July 2026.
  4. [4]Gayoso-Diz P, Otero-González A, Rodriguez-Alvarez MX, Gude F, García F, De Francisco A, Quintela AG. "Insulin resistance (HOMA-IR) cut-off values and the metabolic syndrome in a general adult population: effect of gender and age: EPIRCE cross-sectional study." BMC Endocrine Disorders. 2013;13:47. doi:10.1186/1472-6823-13-47. Independent statement of the equation and units ('fasting serum insulin (μU/ml) × fasting plasma glucose (mmol l⁻¹)/22.5'); source of the population cut-offs quoted on this page (men 1.85 ATPIII / 2.05 IDF; women 2.31 at 30, 2.07 at 50, 2.47 at 70; 3.46 at the 90th percentile) from 2,459 Spanish adults, and of the statement that cut-offs 'are different according to ethnicity, clinical methods of estimation, and metabolic conditions'. Open access; retrieved 29 July 2026.
  5. [5]Wallace TM, Levy JC, Matthews DR. "Use and abuse of HOMA modeling." Diabetes Care. 2004;27(6):1487-1495. doi:10.2337/diacare.27.6.1487. The standard review of appropriate and inappropriate uses of HOMA, and of the relationship between the 1985 approximation formulae and the later computer model. Publisher full text paywalled; open bibliographic record with abstract at Oxford University Research Archive, retrieved 29 July 2026. Cited for the HOMA1/HOMA2 distinction only.
  6. [6]International Union of Pure and Applied Chemistry, Commission on Isotopic Abundances and Atomic Weights. Standard atomic weights, 2023 abridged table: C = 12.011, H = 1.0080, O = 15.999. Used to derive the glucose molar mass 180.156 g/mol and hence the exact mg/dL-to-mmol/L factor of 18.0156 that this calculator uses in place of the rounded 18 embedded in the conventional 405 divisor. Retrieved 29 July 2026.

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