Glossary
Insulin resistance
In one group of people the threshold for insulin resistance moved from 3.46 to 2.05, and nothing about those people had changed except the statistical rule somebody applied to them. Picture a woman whose result comes back at 2.5. Under one rule she is insulin resistant, and under the other she is unremarkable.
What the research found.
One study took a random sample of 2,459 Spanish adults and set a HOMA-IR threshold for insulin resistance two different ways. Taking the top tenth of the group gave 3.46. Counting the parts of metabolic syndrome instead gave 2.05, which means a result of 2.5 gets you labelled resistant under one rule and unremarkable under the other.
Splitting that group by sex and age moved the best value again, so the label depends partly on who is doing the labelling. Men without diabetes came out at 1.85 by one rule. Women without diabetes ran from 2.07 at age 50 to 2.47 at age 70, and every one of those values fell between the 70th and 75th percentiles, meaning 25 to 30 of every 100 ordinary adults sit above the line.
One study of 413 people with rheumatoid arthritis or lupus found the rheumatoid arthritis patients more insulin resistant than the lupus patients. Insulin sensitivity was lower by 27 points, with the true difference falling somewhere between 9 points and 46 points lower. That range never reaches zero, so the direction is settled.
Quevedo-Abeledo and colleagues, Journal of Rheumatology, 2020
In that study the odds of meeting the definition were 2.15 times higher in rheumatoid arthritis than in lupus. The range around it runs from 1.25 to 3.69. That range is the honest part, because the real figure could be a modest quarter higher or close to four times higher, and 413 people aren't enough to settle which.
Quevedo-Abeledo and colleagues, Journal of Rheumatology, 2020
What the term describes
Insulin's job is to move glucose out of your blood and into the tissue that needs it, and insulin resistance means that process has started working less efficiently than it should. Your body answers by making more insulin, which for years keeps your glucose where it belongs and keeps everything looking unremarkable from outside. What the phrase describes is a range rather than a condition you either have or don't.
It underlies a range of metabolic problems without ever being a disease in its own right, which is part of why the term gets used so loosely. It appears on a rheumatology site for two reasons worth separating. Inflammatory arthritis seems to come with more of it, and heart risk is raised in nearly every inflammatory rheumatic condition, so metabolic measurements belong in that wider picture whether or not anybody mentions your joints.
Measuring insulin resistance directly needs a research procedure rather than a blood draw, so in ordinary practice it gets estimated. The usual estimate is called HOMA-IR, worked out from a fasting glucose and a fasting insulin taken together. Being an estimate built from two numbers, it inherits whatever affects either of them, including how long you'd really fasted before the needle went in.
The number that has no normal value
Here's the most useful thing to know about HOMA-IR, and it surprises nearly everybody who has been handed one. There isn't an agreed threshold. That's not a hole in the literature waiting for somebody to fill it, it follows from how the boundary has to be set in the first place. No outcome defines where insulin resistance begins, so the line has to be drawn statistically, and reasonable people draw it in different places.
One study took a random sample of 2,459 Spanish adults aged 20 to 92 and showed how much that choice changes things. Taking the top tenth of the group put the threshold at 3.46. Counting the parts of metabolic syndrome instead put it at 2.05, so picture a woman whose result comes back at 2.5: under the second rule she's insulin resistant, under the first she's unremarkable, and her blood test never changed.
Splitting that group by sex and age moved the value yet again. Men without diabetes came out at 1.85 by one rule and 2.27 by another, while women without diabetes ran from 2.07 at age 50 up to 2.47 at age 70. People with diabetes came out lower still, at 1.60 in men and 1.58 in women.
What that means for reading your own result
Every one of those best values fell between the 70th and 75th percentiles of the group, and that translation is the part worth having. It means the boundary gets drawn low enough that 25 to 30 of every 100 ordinary adults sit above it. Being called insulin resistant puts you in company with roughly a quarter of the adults around you, which isn't the impression most people take from the phrase.
The practical result follows from that. A HOMA-IR figure quoted without the rule behind it isn't telling you much, so when somebody says your result is high, the two questions worth asking are high against which threshold, and whether that threshold came from people like you. Anywhere between 2.05 and 3.46 your label depends on who is doing the labelling rather than on anything happening in your body.
None of that makes the calculation useless, and I don't want to leave you thinking it does. HOMA-IR is a reasonable tool for describing a population and a rough one for describing a person, which is an ordinary state of affairs for any estimate. The error worth avoiding is treating one figure as a verdict about you.
Why it appears on a rheumatology site
One study in our sources compared insulin resistance between two autoimmune diseases seen in one clinic, covering 413 people, of whom 227 had rheumatoid arthritis and 186 had lupus. The rheumatoid arthritis patients were more insulin resistant. Insulin sensitivity was lower by 27 points, with the true difference falling somewhere between 9 points and 46 points lower, at a P value of 0.004.
That range is worth understanding, because it's how these studies tell you what they do and don't know. The best estimate is 27 points, and the honest answer is that the real difference lies somewhere between 9 and 46. Since the range never reaches zero, the direction is settled: rheumatoid arthritis patients really were less sensitive, even though how much less is still open.
Those patients also more often met the definition of insulin resistance outright, at odds 2.15 times higher, across a range from 1.25 to 3.69. Beta cell function went the other way, coming out higher in rheumatoid arthritis by 38 points, from 23 to 52, at a P value below 0.001. Everybody in that study was measured at a single moment rather than followed over years, so it shows you a real difference between two groups of patients and leaves the reason to a rheumatologist who knows the person in front of her.
The problem with that odds ratio
Our own record for that study flags one thing as critical, and it's the difficulty the threshold data already described. The definition applied to those 413 patients was imported from general adults rather than worked out in people with inflammatory arthritis. It was HOMA2-IR at or above 1.85 in men, and in women it was above 2.36 at age 30, above 2.07 at age 50, and above 2.47 at age 70.
A line drawn in one population and applied to another can invent a difference or bury one, which is why this page raises it rather than quoting the headline and moving on. People with inflammatory arthritis may differ from general adults in body composition, activity, or medication, and if they do, a line drawn elsewhere won't sit where it should on their spread. The figure of 2.15 depends entirely on where that line was put.
That isn't a reason to dismiss the finding, and I'd rather you didn't. The continuous measures pointed in that direction too without depending on any threshold, so insulin sensitivity lower by 27 points is a difference in what was measured rather than a difference in which box somebody was sorted into. Quote the continuous result alongside the odds ratio, because the odds ratio on its own tells you less than it appears to.
Before you have the test
The question nearly everybody brings is what moves insulin resistance, and this site holds no treatment source for it in autoimmune disease. There's no honest figure here for what a particular diet does to a HOMA-IR result in rheumatoid arthritis, or what an exercise program does, or what a supplement does. That absence is recorded rather than filled in with an estimate, because an estimate dressed as a finding is the thing this site exists to avoid.
The threshold moves between 2.05 and 3.46 depending on the rule chosen, and no outcome study in our sources ties a HOMA-IR value to anything that happens later in autoimmune disease. A measurement with no agreed boundary and nothing attached to it downstream is genuinely hard to act on. You deserve to know that before the blood is drawn rather than afterwards.
So here's the question worth asking first. What would change as a result of the number? If the answer is a conversation about activity and diet that would be worth having anyway, then the test adds confirmation rather than information, which is fine as long as everybody knows that's what it's doing. If somebody has promised you a specific drop from a specific thing, asking them for the reference is entirely reasonable.
Common misconceptions.
Myth. There's a normal HOMA-IR value I should be under.
Reality. There isn't, and the spread between published thresholds is wide enough to move you from one side of the line to the other. In a group of 2,459 adults, taking the top tenth gave 3.46 while counting the parts of metabolic syndrome gave 2.05, so a woman at 2.5 is resistant under one rule and unremarkable under the other. Splitting by sex and age moved it yet again, which is why a figure quoted without the rule behind it tells you almost nothing.
Myth. A HOMA-IR above the cut-off means I'm diabetic.
Reality. These are two measurements answering two different questions, and one doesn't stand in for the other. HOMA-IR estimates how readily your tissues answer insulin, worked out from a fasting glucose and a fasting insulin, while diabetes is diagnosed on glucose rules instead. Look at where the line falls: every best value in that Spanish study fell between the 70th and 75th percentiles, so being above it puts you with roughly a quarter of all adults rather than in a small, unwell minority.
Myth. This has nothing to do with my arthritis.
Reality. The one study in our sources comparing two autoimmune diseases head to head suggests otherwise, and it covered 413 people. Rheumatoid arthritis patients were more insulin resistant than lupus patients, with insulin sensitivity lower by 27 points and odds of meeting the definition 2.15 times higher. Everybody was measured at a single moment rather than followed over years, so the study shows you a difference and leaves the reason to your rheumatologist.
Myth. The rheumatology figures used a rheumatology threshold.
Reality. They didn't, and the study says so itself, which is why this page raises it rather than quoting the headline and moving on. The definition applied to those 413 patients came from general adults: 1.85 or above in men, and between 2.07 and 2.47 in women depending on age. A line drawn in one population and applied to another can invent a difference or bury one, and that's worth knowing before anybody quotes you the figure of 2.15.
Related terms.
- HOMA-IR, the calculation itself and what goes into it.
- HOMA-IR calculator, which shows what your own fasting numbers produce.
- Rheumatoid arthritis and blood tests, for where this sits among the other measurements.
- Inflammation, and the difference between the kind you can measure and the kind you have.
Questions patients ask.
What is insulin resistance?
It means your tissues answer insulin less efficiently than they should, so more insulin is needed to move your glucose along. The term describes a range rather than a condition you either have or don't have, which is part of why it gets used so loosely. Measuring it directly needs a research procedure rather than a blood draw, so in practice it gets estimated.
What is HOMA-IR?
It's a calculation that estimates insulin resistance from a fasting glucose and a fasting insulin, which is why it stands in for a direct measurement most laboratories can't offer. Being an estimate built from two numbers, it inherits everything that affects either of them, including how long you'd really fasted. That makes it a reasonable tool for describing a population and a rough one for describing you.
What number should I aim for?
This page won't hand you one, because the published thresholds disagree too much for a target to mean anything. In one group the cut-off moved from 3.46 to 2.05 when the rule changed, and splitting by sex and age moved it again, from 1.85 in men to 2.47 in women at age 70. A target quoted without the rule behind it isn't really a target at all.
Why do the thresholds vary so much?
No outcome defines where the boundary belongs, so somebody has to choose it statistically, and reasonable people choose differently. One rule takes the top tenth of a group and calls everything above it resistant, while another uses the parts of metabolic syndrome. Those two gave 3.46 and 2.05 in one sample, and every best value fell between the 70th and 75th percentiles, which tells you how ordinary the state is.
Do people with inflammatory arthritis have more of it?
One study compared two diseases in 413 people and found rheumatoid arthritis patients more insulin resistant than lupus patients. Insulin sensitivity was lower by 27 points. The odds of meeting the definition were 2.15 times higher, and everybody was measured at one moment rather than followed over years, so it shows a real difference between two groups and leaves the reason open.
What does an odds ratio of 2.15 mean for me in practice?
It compares two groups rather than describing you, which is the first thing to know. Odds a bit more than doubled means that if you lined up both groups, noticeably more of the rheumatoid arthritis side would sit above the line, though not double the number. The range from 1.25 to 3.69 is the useful part, because it says the real figure could be a quarter higher or nearly four times higher.
Should I ask for the test?
That's a conversation with your own team rather than something a page settles, though knowing the limits beforehand makes it a better conversation. A single HOMA-IR figure gets sorted against a threshold that moves between 2.05 and 3.46, so on its own it won't tell you much. Ask what would change as a result of the number, because that question settles whether it's worth doing.
Can I change it?
This site holds no source on treating insulin resistance in autoimmune disease, so there's no honest figure here for what moves it or by how much. That absence is real rather than an oversight, and it's the question most people bring with them. If anybody has promised you a specific drop from a specific diet or supplement, asking them for the reference is entirely reasonable.
References.
- Gayoso-Diz P; Otero-González A; Rodriguez-Alvarez M et al. 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. 10.1186/1472-6823-13-47Cross-sectional random population sample of 2
- Quevedo-Abeledo J; Sánchez-Pérez H; Tejera-Segura B et al. Higher Prevalence and Degree of Insulin Resistance in Patients With Rheumatoid Arthritis Than in Patients With Systemic Lupus Erythematosus. The Journal of Rheumatology. 2020;48:339-347. 10.3899/jrheum.200435Cross-sectional study of 413 subjects
This page gathers the published research on this subject into one place. The studies behind it were published between 1989 and 2026, and every figure links to the paper it came from. Those studies were peer reviewed. This summary of them was not. Dr. Sarah Luebker is reviewing these pages one at a time and has not reached this one yet, so it carries no medical review date and nothing here is her opinion or her advice to you. Each page gets updated as she reaches it. It is here in the meantime because the science is worth having in one organized place that is easy to find and easy to read. Talk to your own clinician before acting on any of it.