Home
/

What is an Atherogenic Index of Plasma Blood Test?

REVIEWED BY
Bill Maish, MD
Clinical Content Consultant
Published
May 30, 2026
Last updated
May 30, 2026
Quick answer:

The Atherogenic Index of Plasma (AIP) is the logarithmic ratio of triglycerides to HDL cholesterol that reflects the balance between artery-clogging remnant particles and protective HDL. Values below 0.11 are associated with lower cardiovascular risk, 0.11–0.24 with average risk, and above 0.24 with higher risk. AIP complements standard cholesterol markers to help assess risk for atherosclerosis, metabolic syndrome, and fatty liver.

Read more →
Table of contents

AIP: A Log-Ratio Snapshot of Lipid Particle Quality

The Atherogenic Index of Plasma (AIP) is a calculated snapshot of your blood's lipid mix. It combines two routine lipid values—triglycerides and HDL cholesterol—to summarize how fats made in the liver and absorbed from the gut travel in the bloodstream inside carrier particles (lipoproteins). AIP isn't a substance you can see under a microscope; it's a single number distilled from these circulating lipids to represent the overall "tone" of your plasma.

AIP matters because it reflects the balance between triglyceride‑rich particles that deliver fat outward and can leave cholesterol behind (VLDL and remnants) and HDL particles that help carry cholesterol back to the liver for disposal (reverse cholesterol transport). That balance influences the formation of small, dense LDL particles and remnant lipoproteins—forms more apt to slip into artery walls and fuel plaque buildup (atherogenesis). In short, AIP captures the atherogenic character of your plasma and serves as a practical proxy for lipoprotein particle quality and behavior (small, dense LDL; remnant lipoproteins), condensing complex lipid biology into one clinically useful index.

Why "Stickiness" of Blood Lipids Matters

The Atherogenic Index of Plasma (AIP) distills how "sticky" your blood lipids are by comparing triglycerides to HDL cholesterol. It reflects the balance between particles that deposit cholesterol in artery walls and those that carry it away, linking lipid metabolism with vascular health, insulin signaling, and liver fat handling.

Reading an AIP Value

In general, lower values are better. Values below about 0.11 are associated with lower cardiovascular risk, 0.11–0.24 with average risk, and above 0.24 with higher risk. When AIP is low or even negative, triglycerides are modest and HDL is effective, favoring larger, less harmful LDL particles and efficient reverse cholesterol transport. This pattern aligns with better insulin sensitivity and supple arteries. People usually feel well; there are no specific symptoms. Men tend to have slightly higher AIP than women, and it often rises after menopause. In children and teens, low AIP tracks with healthier weight and metabolic profiles.

When AIP is high, the blood carries more triglyceride-rich remnants and small, dense LDL—particles that penetrate the artery wall, inflame the endothelium, and promote plaque. It often travels with insulin resistance, abdominal obesity, higher blood pressure, and fatty liver. Most people feel nothing, though very high triglycerides can precede pancreatitis. During pregnancy, triglycerides naturally rise, so AIP may increase; markedly elevated values can signal heightened cardiometabolic stress.

Low values usually reflect low triglycerides and/or higher HDL, indicating efficient fat clearance (lipoprotein lipase activity), effective reverse cholesterol transport, and larger, less harmful LDL particles. Systemically this aligns with better metabolic flexibility and vascular resilience. Lower AIP is more typical in younger people and premenopausal women.

High values usually reflect high triglycerides relative to HDL, pointing to insulin resistance, increased hepatic VLDL output, impaired HDL maturation, and a shift toward small, dense LDL. System effects include higher plaque propensity, endothelial dysfunction, and association with fatty liver. Higher AIP is more common in men, with aging, and after menopause; it also rises in normal pregnancy, especially late gestation.

What Can Move an AIP Number

AIP is sensitive to fasting status, recent alcohol, acute illness, and thyroid or kidney disorders. Estrogens, steroids, beta‑blockers, retinoids, and some antivirals can shift values. Pregnancy physiologically elevates AIP. Consistent unit conventions help when comparing results across labs or time.

AIP integrates the liver's VLDL output, HDL function, and glucose–insulin dynamics. It complements LDL and non-HDL cholesterol to estimate lifetime risk for atherosclerosis, type 2 diabetes progression, fatty liver, heart attack, and stroke. Lower AIP suggests a more resilient cardiometabolic system.

What AIP Adds Beyond a Standard Lipid Panel

Being in range suggests balanced lipoprotein metabolism, with controlled VLDL production and adequate HDL-mediated cholesterol recycling. This pattern supports stable glucose–lipid signaling and lower atherogenic burden; consensus generally places "within reference ranges" toward the lower end of the usual range.

FAQs

It’s a calculated score—log10(triglycerides ÷ HDL-C, in mmol/L)—derived from a standard lipid panel to capture lipid particle quality and remnant burden.

AIP integrates triglycerides and HDL into a single risk marker, revealing small, dense LDL patterns and metabolic stress that LDL-C may miss.

Retest every 6–12 weeks during lifestyle or medication changes, then periodically for long-term tracking. Use consistent fasting status and timing.

Diet quality (refined carbs, added sugars, alcohol), weight status, activity, sleep, stress, insulin resistance, thyroid and liver health, hormones, and certain medications.

Not always, but fasting (8–12 hours) and avoiding alcohol for 24–48 hours can improve comparability across tests.

Superpower currently offers at-home blood testing in the following states: Alabama, Arizona, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, and Wisconsin.

We’re actively expanding nationwide, with new states being added regularly. If your state isn’t listed yet, stay tuned.

References

  1. Dobiásová, M. (2004). Atherogenic index of plasma [log(triglycerides/HDL-cholesterol)]: Theoretical and practical implications. Clinical Chemistry, 50(7), 1113-1115. https://doi.org/10.1373/clinchem.2004.033175
  2. Millán, J., Pintó, X., Muñoz, A., Zúñiga, M., Rubiés-Prat, J., Pallardo, L. F., Masana, L., Mangas, A., Hernández-Mijares, A., González-Santos, P., Ascaso, J. F., & Pedro-Botet, J. (2009). Lipoprotein ratios: Physiological significance and clinical usefulness in cardiovascular prevention. Vascular Health and Risk Management, 5, 757-765. https://pubmed.ncbi.nlm.nih.gov/19774217/
  3. Murguía-Romero, M., Jiménez-Flores, J. R., Sigrist-Flores, S. C., Espinoza-Camacho, M. A., Jiménez-Morales, M., Piña, E., Méndez-Cruz, A. R., Villalobos-Molina, R., & Reaven, G. M. (2013). Plasma triglyceride/HDL-cholesterol ratio, insulin resistance, and cardiometabolic risk in young adults. Journal of Lipid Research, 54(10), 2795-2799. https://doi.org/10.1194/jlr.M040584
  4. Nordestgaard, B. G. (2016). Triglyceride-rich lipoproteins and atherosclerotic cardiovascular disease: New insights from epidemiology, genetics, and biology. Circulation Research, 118(4), 547-563. https://doi.org/10.1161/CIRCRESAHA.115.306249
  5. Varbo, A., Benn, M., Tybjærg-Hansen, A., & Nordestgaard, B. G. (2013). Elevated remnant cholesterol causes both low-grade inflammation and ischemic heart disease, whereas elevated low-density lipoprotein cholesterol causes ischemic heart disease without inflammation. Circulation, 128(12), 1298-1309. https://doi.org/10.1161/CIRCULATIONAHA.113.003008

Built by the world’s top doctors and scientists

Dr Anant Vinjamoori, MD

Chief Longevity Officer, Superpower

Board-certified longevity physician. Previously product leader at Virta Health & CMO at Modern Age. Featured in  WSJ, Forbes, and Fortune.

Learn more

Dr Leigh Erin Connealy, MD

Clinician & Founder of The Centre for New Medicine

Leads the largest integrative medical clinic in North America. A pioneer in integrative oncology.

Learn more

Dr Robert Lufkin

UCLA Medical Professor, NYT Bestselling Author

A leading voice on metabolic health and longevity as shown in The Today Show, USA Today and FOX.

Learn more

Dr Abe Malkin

Founder & Medical Director of Concierge MD

Leads a nationwide medical practice, and Drip Hydration, a mobile IV therapeutics company

Learn more
Membership slide 1
Membership slide 1
Membership slide 2
Membership slide 3
1 / 3

Your membership starts here

Annual 100+ biomarker panel

Data dashboard and digital twin

Upload past labs and connect wearables

Personalized health protocol

24/7 care team access

AI companion for all health questions

Marketplace with additional solutions

$199

/year*

Billed annually

HSA/ FSA eligible
Cancel anytime
Results in a week

* Pricing may vary for members in New York and New Jersey