Understanding your results

Triglyceride/HDL ratio: how it is calculated, table of values and what it means

How to calculate the triglyceride/HDL ratio from your blood test, which cut-offs research proposes, including Mexican studies, and which data give it meaning.

Understanding your resultsPublished on November 5, 202620 min read
Written by
Oleg Kainara
Founder of Previva

Visionary entrepreneur driving innovation at the intersection of healthcare, AI and global diagnostics. Author of the Previva methodologies. He has worked for many years in preventive medicine, longevity and early detection of disease. He writes from his own experience and vision.

Reviewed by
Medical review pending

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Key points

  • The triglyceride/HDL ratio is calculated by dividing triglycerides by HDL cholesterol from the same fasting lipid panel, both in mg/dL. Triglycerides of 155 with HDL of 45 give 3.4; triglycerides of 90 with HDL of 60 give 1.5.
  • It is read as an indirect marker of insulin resistance and of small, dense LDL, because insulin resistance raises triglycerides and lowers HDL at the same time. It is a clue, not a diagnosis.
  • There is no single cut-off: the original studies propose 3.0 and 3.5; in Mexican adults 3.46 has been proposed against metabolic syndrome; cut-offs in women tend to be lower than in men. Below 2 you are under every proposed cut-off; above 3.5 you exceed them all.
  • The ratio is only valid with a sample taken after 9 to 12 hours of fasting, in mg/dL: with values in mmol/L the number is different. Alcohol, a heavy dinner, illness and some medicines move it without your metabolism having changed.

The triglyceride HDL ratio is not printed on most lipid panels in Mexico, but it can be calculated in ten seconds from two values that almost all of them include: triglycerides and HDL cholesterol. It is a quotient that research has used for twenty years as an indirect marker of insulin resistance and of a smaller, denser type of LDL cholesterol. The first thing to know is that it is a clue, not a diagnosis; the second, that there is no single cut-off, because the thresholds change with the population, with sex and with the units the laboratory uses. This text explains where the number comes from, how to calculate it with five worked examples, which cut-offs research has proposed, including Mexican research, what moves it without your metabolism having changed, and why it is not calculated from a non-fasting sample (on how to prepare, see fasting before a blood test).

What the triglyceride/HDL ratio is and what it tries to measure

Triglycerides are the form in which blood carries fat; HDL cholesterol is the lipoprotein that collects cholesterol from tissues and returns it to the liver, which is why it is called "good".[9][10] In a person without insulin resistance the two values usually run in opposite directions: moderate triglycerides, high HDL. Insulin resistance breaks that balance in both directions at once. Insulin normally restrains the release of fatty acids from body fat; when cells respond less to it, that release runs "unchecked", the liver receives more fatty acids and makes more triglycerides, which it packs into VLDL particles and sends into the blood.[5] At the same time the activity of an enzyme that breaks down HDL increases, HDL particles become smaller and less stable, and the production of their main protein, apolipoprotein A-I, falls.[5]

That is why the ratio makes sense: when triglycerides rise and HDL falls for the same reason, dividing one by the other amplifies the signal. The group of Gerald Reaven at Stanford tested it in 2003 in 258 overweight adults without diabetes, measuring insulin resistance with the reference method (the insulin suppression test) and comparing it with the markers any laboratory reports. A triglyceride cut-off of 130 mg/dL identified insulin-resistant people with 67 % sensitivity and 71 % specificity; a TG/HDL ratio of 3.0, with 64 % and 68 %; fasting insulin was more specific (85 %) but less sensitive (57 %).[1] Their conclusion was pragmatic: without a standardized insulin assay, triglycerides or the TG/HDL ratio were the most practical way to identify who was insulin resistant.[1]

Two years later the same group expanded the sample to 449 apparently healthy adults for insulin resistance and 1135 for LDL particle size. Of all the routine measurements, the triglyceride/HDL ratio was "the best predictor" of both insulin resistance and LDL diameter, with an optimal cut-off of 3.5; and sensitivity and specificity were "even greater" for identifying those with small, dense LDL.[2] That is the second reason the ratio matters: small, dense LDL is the form of cholesterol a recent Mexican paper calls "the most concerning aspect" of atherogenic dyslipidemia, and the ratio detects it better than total LDL does.[4] If your LDL came back high, the context is in high cholesterol: what it means and what to do.

The TG/HDL ratio and HOMA-IR try to estimate the same thing, insulin resistance, by different routes: HOMA multiplies glucose by insulin, and the ratio divides two fats. The practical advantage of the ratio is that it does not require ordering insulin, which in Mexico rarely comes in the basic panel; its limit is that the two figures that form it also move for reasons that have nothing to do with insulin. In the Mexican study of 1318 adults, the ratio was associated both with metabolic syndrome and with the HOMA2-IR index, meaning the two estimates point in the same direction in this population.[3]

How it is calculated: the formula and five worked examples

The formula is a direct division: TG/HDL ratio = triglycerides (mg/dL) / HDL cholesterol (mg/dL). Both values must come from the same lipid panel, taken fasting, and be in the same units. In Mexico laboratories report in mg/dL, and every cut-off on this page is in those units.[1][3] An example with the numbers people search for most: triglycerides of 155 and HDL of 45. Divide 155 by 45 and you get 3.44. The table gathers five cases so you can place yours:

Triglycerides (mg/dL)HDL (mg/dL)TG/HDL ratioWhat it usually indicatesWhat to measure and record
90601.50Healthy triglycerides (under 150) and HDL above 40 and 50.[9][10] Below every proposed cut-off.Save with date as a baseline; repeat in 5 years if there are no risk factors.[8]
155453.44Borderline triglycerides (150 to 199); HDL normal for a man, low for a woman (under 50).[9][10] Exceeds 3.0 and nearly reaches the 3.46 proposed in Mexico.[1][3]Hours of fasting and alcohol the night before; waist; fasting glucose; repeat in 2 to 3 months.
161384.24Borderline triglycerides with HDL below 40 in both sexes.[9][10] Exceeds every proposed cut-off.[1][2][3]Waist, home blood pressure, fasting glucose and HbA1c: the other criteria of metabolic syndrome.[7]
250505.00High triglycerides (200 to 499); HDL at the limit for a woman, normal for a man.[9][10] Intermediate band of the Mexico City quartiles (4.7 to 6).[4]All of the above plus medicines, alcohol and sugar; an appointment without urgency but without postponing it.
4663214.56Triglycerides close to the 500 threshold the guidelines call "very high", and low HDL.[9] A two-digit ratio is no longer a marker: the absolute triglyceride value matters.Appointment in the coming days; repeat after a strict fast; ask about secondary causes and family history.[8][9]

Two details from the table. First: with triglycerides of 155, a man with HDL of 45 is within the healthy range and a woman is below her threshold of 50, even though the ratio is identical; that is why sex-specific cut-offs exist.[10] Second: when triglycerides go above 400 or 500, the ratio stops being useful, because any HDL gives a huge quotient and the question changes to why triglycerides are so high.[6][9] We wrote about that in high triglycerides: what it means and what to check.

If your laboratory reports in mmol/L

Outside Mexico many laboratories report lipids in mmol/L, and there the ratio changes its number even though the blood is the same, because triglycerides and cholesterol convert with different factors. The European lipid consensus equates 1.7 mmol/L of triglycerides with 150 mg/dL, and 1.0 mmol/L of HDL with 40 mg/dL.[6] If you divide in mg/dL, 150 by 40 gives 3.75; if you divide the same values in mmol/L, 1.7 by 1.0 gives 1.7. The result in mmol/L comes out more than two times smaller, so a cut-off of 3.0 or 3.5 designed in mg/dL cannot be applied to a result in mmol/L without first converting each value. If you have results of both kinds, convert them all to mg/dL before comparing, and remember that the printed reference range is not your personal norm.

What does a TG/HDL ratio of 2, 3.5 or 5 mean?

A ratio of 2 is below every cut-off proposed for adults, including the lowest ones suggested for women; a ratio of 3.5 matches the optimal cut-off of the 2005 Stanford study and practically the 3.46 proposed for Mexican adults against metabolic syndrome; and a ratio of 5 exceeds every cut-off and falls in the intermediate band of the quartiles measured in Mexico City.[2][3][4][5] That is the short answer. The long one is that each cut-off comes from a different population, method and question, and it is worth knowing where each number comes from before applying it to your result:

StudyPopulation and methodProposed cut-off or range
McLaughlin et al. (2003), Annals of Internal Medicine258 overweight adults without diabetes, United States; insulin suppression test3.0 (sensitivity 64 %, specificity 68 %)[1]
McLaughlin et al. (2005), American Journal of Cardiology449 apparently healthy adults for insulin resistance and 1135 for LDL size3.5, the best predictor among routine measurements; even better for small, dense LDL[2]
Baez-Duarte et al. (2022), Gaceta Médica de México1318 adults aged 18 to 80 from central Mexico; metabolic syndrome criteria adapted to the Mexican population; 10 to 12 hours of fasting3.46 optimal (sensitivity 79.6 %, specificity 76.4 %); 3.0 for screening (86.9 % and 66.8 %), not for confirmation[3]
Nájera et al. (2025), Cardiovascular and Metabolic Science68,000 adults from Mexico City, 2012 to 2022; quartiles of the population itselfLiterature averages: 2.7 in women and 3.4 in men. Quartile bands: under 3.3 low, 3.3 to 4.6 borderline, 4.7 to 6 intermediate, above 6 high[4]
Baneu et al. (2024), Biomedicines, review of 17 studiesAdults from several countries and backgroundsMedian of the cut-offs: 2.53 in women and 2.8 in men; in African American populations, 1.5 and 2[5]

Look at the third row. In the same Mexican population the cut-off is 3.46 if the question is "which value best separates those who already meet metabolic syndrome criteria" and 3.0 if the question is "which value lets fewer cases slip through", at the cost of more false positives; that is why the authors propose 3.0 for screening and not for confirmation.[3] In that study, people without metabolic syndrome had an average ratio of 2.9 (median 2.3) and those with it, 6.6 (median 5.2): the distance between the two groups is large, but the ranges overlap, and that is where the ratios of 3 to 4 that generate most doubts live.[3]

Practical reading: between 2 and 3 the cut-offs proposed for women and for some populations begin, and context decides; between 3 and 3.5 you cross the cut-offs of the original studies and of the Mexican one; above 4.6 you are in the upper half of what was measured in Mexico City.[1][2][3][4][5] None of this is a diagnosis: the ratio points to a pattern that the doctor confirms or rules out with waist, blood pressure, glucose and, if needed, insulin.

Why cut-offs depend on population, sex and units

Women before menopause tend to have lower triglycerides and higher HDL than men, so the same degree of insulin resistance produces a smaller ratio in them; that is why almost every study that separates by sex finds lower cut-offs in women, and the 2024 review also notes that the ratio is more accurate in men than in women.[5] The HDL threshold the guidelines use reflects the same thing: below 40 mg/dL is low in men and below 50 in women.[7][10] In the Mexico City cohort the median was 2.84 in women and 3.24 in men, and the mean 3.63 and 4.62.[4]

Ancestry matters too. The review of 17 studies finds that the ratio "demonstrates greater accuracy" in people of European, Asian and Hispanic background than in African American populations, where the proposed cut-offs drop to 1.5 in women and 2 in men.[5] For the Mexican population there are at least two studies of its own: the one of 1318 adults from the center of the country, with the 3.46 cut-off, and the cohort of 68,000 people from Mexico City, whose authors warn that the ratio "varies significantly across ethnicities and clinical conditions" and propose reading it by quartiles of the population itself.[3][4] And one general limit: in most studies the ability of the ratio to classify people correctly (the area under the curve) "virtually never surpasses" 0.8, that is, it gets most cases right and a non-trivial minority wrong.[5]

The Mexican context explains why the ratio draws so much interest here. According to the national ENSANUT 2020 survey cited in the Mexico City paper, 48.9 % of adults had hypertriglyceridemia and 28.3 % had HDL below 40 mg/dL (21.6 % of women and 35.5 % of men).[4] The Mexican Official Standard on dyslipidemias defines hypertriglyceridemia as triglycerides above 150 mg/dL and hypoalphalipoproteinemia as HDL below 40.[8]

What moves the ratio without changing your metabolism

The ratio divides the value in the lipid panel that moves most from one day to the next, triglycerides, by one of the most stable, HDL. Any deviation in triglycerides passes straight into the ratio. This is what most often distorts an isolated result:

  • Incomplete fast. The Mexican Official Standard requires 9 to 12 hours of fasting to measure triglycerides, although total cholesterol and HDL can be measured without fasting.[8] The European consensus measured how much triglycerides rise after a habitual meal: on average up to 0.3 mmol/L, about 26 mg/dL, 1 to 6 hours later; little for someone with triglycerides of 90, enough to cross a cut-off if you are at 140.[6] With triglycerides of 155 and HDL of 45, those 26 mg/dL move the ratio from 3.44 to 2.87 or to 4.02 depending on which side they fall.
  • Heavy dinner or alcohol the night before. Excessive alcohol and a diet high in fat and sugar are among the causes of high triglycerides the NIH list, and sustained alcohol also lowers HDL indirectly through weight.[9][10] A single unusual night does not change your metabolism, but it does change the next morning sample.
  • Illness, thyroid, liver and kidney. Kidney, liver and thyroid disease, poorly controlled diabetes and overweight are on the list of conditions that raise triglycerides.[9] A cold the week before is not on the guideline lists, but the general principle of repeating under stable conditions before concluding is.
  • Medicines. Some diuretics and certain treatments for high blood pressure, breast cancer and HIV raise triglycerides; beta blockers, anabolic steroids, the progestins in some contraceptives and menopause therapies, and benzodiazepines lower HDL.[9][10] A new medicine between two panels can explain the whole change in the ratio. Do not stop anything on your own: write it down and discuss it.
  • Very high triglycerides. If a non-fasting sample comes back with triglycerides above 440 mg/dL, the European consensus recommends repeating it fasting; and above 400, the usual formula for calculating LDL is no longer valid, so the whole panel is recalculated.[6]

What to do with the result and when to repeat it

  • Ratio below 2 with triglycerides below 150 and HDL above 40 or 50. Save it with its date as a baseline. The Mexican Official Standard indicates repeating the lipid panel every 5 years from age 20 if there are no risk factors, and every 1 to 2 years if there are; MedlinePlus agrees and adds that men aged 45 to 65 and women aged 55 to 65 are checked every 1 to 2 years.[8][10] What else to include in that check-up is in annual preventive check-up.
  • Ratio between 2 and 3.5 with a single value out of place. Look at each value separately: high triglycerides with normal HDL have different causes than low HDL with normal triglycerides. Note alcohol, sugar, medicines and smoking, and repeat in 2 to 3 months at the same laboratory after 9 to 12 hours of fasting.[8][9][10]
  • Ratio above 3.5 with triglycerides of 150 or more and low HDL. Add what is missing so the pattern has context: waist, home blood pressure for seven days, fasting glucose and HbA1c. Triglycerides of 150 or more, HDL below 40 or 50, blood pressure of 130/85 or more, fasting glucose of 100 or more and a grown waist are the five criteria of metabolic syndrome; three of five make the diagnosis, and the doctor decides that.[3][7] Book an appointment in the coming weeks. If the reason for looking at the ratio was that you are not losing weight or that you get sleepy after meals, bring that too: the ratio does not explain the symptom on its own, but it organizes the conversation.
  • Triglycerides persistently at 175 or more. The AHA/ACC cholesterol guideline considers them a risk-enhancing factor regardless of the ratio, and takes them into account when deciding together with LDL and overall risk.[7] It is a piece of data for the appointment, not for the calculator.
  • What the guidelines associate with lower triglycerides and higher HDL. The NIH list heart-healthy eating, regular physical activity, a healthy weight, quitting smoking, good sleep and limiting alcohol; MedlinePlus adds that losing weight, especially around the waist, and 30 minutes of aerobic exercise most days raise HDL.[9][10] What to change and by how much is decided with the doctor, with your data in front of you.
  • When to repeat. There is no fixed frequency for the ratio itself. What helps is repeating the full panel under the same conditions and at the same laboratory, months apart, to see the direction of change in triglycerides and HDL separately and not the noise of one morning.[6][8]

Warning signs

High triglycerides and low HDL cause no symptoms: the NIH say it plainly, they "usually do not cause any symptoms".[9] What does require not waiting for the next check-up is the absolute triglyceride value when it shoots up, because the risk stops being the heart in the long term and becomes the pancreas in the short term.

  • Triglycerides of 500 mg/dL or more. The guidelines call them "very high"; at that level they can cause acute pancreatitis, changes in the blood vessels of the retina and skin lesions on the back, chest, arms and legs.[9] The European consensus sets the referral threshold for pancreatitis risk at triglycerides above 880 mg/dL, and the Mexican Official Standard notes that above 1000 mg/dL the pancreatitis risk is short-term.[6][8] With any of these values, book an appointment in the coming days, not at the next check-up; with 1000 or more, today.
  • Severe pain in the upper abdomen, often with nausea or vomiting, in a person with very high triglycerides is how pancreatitis presents: emergency. The NIH also describe that with triglycerides above 1500 mg/dL there can be stomach pain, enlargement of the liver and spleen and short-term memory loss.[9]
  • Skin lesions (yellowish bumps or plaques on the back, chest, arms, legs or eyelids) accompanying very high triglycerides are the fat deposits the NIH describe as skin damage from very high levels; a reason for a prompt appointment.[9]
  • Very high triglycerides in a young person, or a close relative with very high triglycerides or pancreatitis, point to an inherited disorder of lipid metabolism, and the NIH indicate that in that case genetic testing and checking the family may be needed.[9] The Mexican Official Standard defines familial hypertriglyceridemia from triglycerides above 200 mg/dL with family history, and the AHA/ACC guideline calls for a fasting panel from the first evaluation when there is a family history of premature cardiovascular disease or genetic hyperlipidemia.[7][8]

What to bring to the doctor

An appointment for a high TG/HDL ratio lasts as long as it takes to explain the context. If you arrive with the context in order, the conversation starts where it should: on whether the pattern is real and what else needs measuring.

  1. The complete lipid panel, with triglycerides, HDL, LDL and total cholesterol in their units, date and laboratory. If you have more than one, bring them all: the direction of change says more than the ratio of one morning.[6]
  2. The conditions of the sample: hours of fasting, what you had for dinner and whether there was alcohol the night before, time of the draw, whether you were ill.[6][8]
  3. Recent waist and weight, and whether you have noticed your waist growing: it is the metabolic syndrome criterion measured at home.[3][7]
  4. Home blood pressure: the seven-day average with an upper-arm device, if you have one.[7] How to take it is in normal blood pressure.
  5. Fasting glucose and HbA1c, with dates, if you have them; if not, bring them as a question, as with fasting insulin.[3][7] The detail on glucose is in high fasting glucose.
  6. History: relatives with a heart attack or stroke at an early age, very high triglycerides or pancreatitis; diabetes in the family.[7][9]
  7. List of medicines and supplements, including diuretics, beta blockers, oral contraceptives, corticosteroids and anabolic steroids, and whether you smoke.[9][10]
  8. Three questions: whether the pattern justifies measuring fasting insulin or HbA1c, which cut-off your doctor uses to interpret the ratio and for which population, and how often to repeat the panel in your case.

What pattern do your lipids show? Seven questions before the appointment

Not a diagnosis: it sorts out which values you have, under what conditions they were taken and what surrounds them, and leaves you with a list of what to record. If you have severe pain in the upper abdomen with nausea or vomiting, or your triglycerides came back at 1000 or more, do not answer anything: seek care today.

Question 1 of 7

Do you have triglycerides and HDL cholesterol from the same test?

This quiz points to what to measure and what to discuss with your doctor. It is not a diagnosis and does not replace an appointment. Your answers never leave your browser.

Frequently asked questions

What triglyceride/HDL ratio is considered good?

There is no single cut-off accepted by the guidelines, because the ratio is not a diagnostic criterion but a research marker. The original studies proposed 3.0 and 3.5; in Mexican adults 3.46 was proposed against metabolic syndrome and 3.0 for screening; the medians of the cut-offs in a review of 17 studies were 2.53 in women and 2.8 in men. Below 2 you are under every proposed cut-off; above 3.5 you exceed them all; in between, context decides. Ask your doctor which cut-off they use and which population it comes from.

My triglycerides are 155 and my HDL is 45: what is my ratio and what does it mean?

Your ratio is 155 divided by 45, that is, 3.44. It exceeds the 3.0 cut-off of the original study and sits just below the 3.46 proposed for Mexican adults and the 3.5 of the 2005 study. Your triglycerides are in the borderline zone (150 to 199) and your HDL is normal if you are a man and low if you are a woman (under 50). Before concluding, check how the sample was taken: hours of fasting, dinner and alcohol the night before. If the fast was correct, add waist, blood pressure and fasting glucose and discuss it at your next appointment; if it was doubtful, repeat in 2 to 3 months at the same laboratory.

Are the cut-offs the same for women and men?

No. Women before menopause tend to have lower triglycerides and higher HDL, so the same degree of insulin resistance produces a smaller ratio in them. Studies that separate by sex find lower cut-offs in women: averages of 2.7 versus 3.4 in men in the literature cited by the Mexico City cohort, and medians of 2.53 versus 2.8 in a review of 17 studies. The threshold for low HDL also differs: under 50 mg/dL in women and under 40 in men. The Mexican study of 1318 adults did not separate by sex and proposed a single cut-off of 3.46.

What matters more, LDL or the TG/HDL ratio?

They measure different things and do not compete. Cholesterol guidelines build the decision around LDL and overall cardiovascular risk, and treat persistent triglycerides of 175 or more as a factor that enhances that risk. The TG/HDL ratio adds what total LDL does not show: how much insulin resistance lies behind it and what share of the LDL is small, dense particles. A high LDL with a low ratio and a normal LDL with a high ratio are two different patterns, and the doctor approaches them differently. Bring both; do not choose one.

How often should the lipid panel be repeated, and under what conditions?

If everything is in order and you have no risk factors, the Mexican Official Standard indicates every 5 years from age 20; with risk factors, every 1 to 2 years; men aged 45 to 65 and women aged 55 to 65, every 1 to 2 years. If a result surprises you, repeat it in 2 to 3 months. The conditions are always the same: in the morning, after 9 to 12 hours of fasting with only water, no alcohol in the previous 24 hours, no recent illness and, if possible, at the same laboratory so results can be compared.

Sources

  1. McLaughlin T, Abbasi F, Cheal K, Chu J, Lamendola C, Reaven G (2003). Use of metabolic markers to identify overweight individuals who are insulin resistant. Annals of Internal Medicine 139(10)
  2. McLaughlin T, Reaven G, Abbasi F et al. (2005). Is there a simple way to identify insulin-resistant individuals at increased risk of cardiovascular disease? American Journal of Cardiology 96(3)
  3. Baez-Duarte BG, Zamora-Ginez I, Rodríguez-Ramírez SO, Pesqueda-Cendejas LK, García-Aragón KH (2022). Índice TG/HDL para identificar a sujetos con síndrome metabólico en población mexicana. Gaceta Médica de México 158(5)
  4. Nájera N, López-Dionicio Y, Meaney A et al. (2025). The TG/HDL-c index, a marker of atherogenic dyslipidemia, is a significant factor in the contemporary epidemiological profile of Mexico. Cardiovascular and Metabolic Science 36(4)
  5. Baneu P, Văcărescu C, Drăgan SR et al. (2024). The Triglyceride/HDL Ratio as a Surrogate Biomarker for Insulin Resistance. Biomedicines 12(7)
  6. Nordestgaard BG, Langsted A, Mora S et al. (2016). Fasting is not routinely required for determination of a lipid profile: joint consensus statement from the European Atherosclerosis Society and European Federation of Clinical Chemistry and Laboratory Medicine. European Heart Journal 37(25)
  7. Grundy SM, Stone NJ, Bailey AL et al. (2019). 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol. Circulation 139(25)
  8. Secretaría de Salud (2012). Norma Oficial Mexicana NOM-037-SSA2-2012, Para la prevención, tratamiento y control de las dislipidemias. Diario Oficial de la Federación
  9. National Heart, Lung, and Blood Institute. High Blood Triglycerides
  10. MedlinePlus, National Library of Medicine. HDL: The "Good" Cholesterol
Written by
Oleg Kainara
Founder of Previva
Reviewed by
Medical review pending
This content is informational and preventive. It is not a medical diagnosis and does not replace a consultation with a health professional. If you have any doubt about your results, talk to your doctor.