Target intelligence / Profile preview

Atherogenic index of plasma (AIP)

Target
AIP
Molecular classification
Biomarker, Clinical index, Lipid ratio
01

Overview

The Atherogenic Index of Plasma (AIP) is a mathematical marker used to predict the risk of atherosclerosis and cardiovascular disease, calculated as the logarithmically transformed ratio of molar concentrations of triglycerides to high-density lipoprotein cholesterol [log10(TG/HDL-C)]. It serves as a surrogate measure for lipoprotein particle size, specifically correlating strongly with the presence of small dense low-density lipoprotein (sdLDL) particles, which are highly pro-atherogenic. Values of AIP below 0.11 are generally associated with low cardiovascular risk, while values above 0.24 indicate high risk. Because AIP is a calculated ratio and not a distinct protein or receptor, it is not a therapeutic target in the traditional sense; instead, it is a clinical biomarker used to assess the efficacy of lipid-lowering therapies. Drugs such as statins, fibrates, and niacin affect the AIP by modulating the individual lipid fractions that comprise the index. In clinical practice, AIP is often considered a more sensitive predictor of coronary artery disease than individual lipid parameters because it reflects the complex balance between atherogenic and protective lipoproteins.

Other names
Log(TG/HDL-C) ratioAtherogenic indexPlasma atherogenic index
02

Mechanism of action

Drugs do not target the AIP directly; rather, they modulate the components of the index by inhibiting HMG-CoA reductase to lower LDL and triglycerides, activating PPAR-alpha to lower triglycerides and raise HDL-C, or inhibiting CETP to increase HDL-C levels, thereby lowering the calculated AIP value.

03

Biological functions

Lipid metabolism indicatorRisk assessmentMetabolic monitoring
04

Disease associations

Cardiovascular diseaseAtherosclerosisMetabolic syndromeDiabetes mellitusCoronary artery diseaseHypertension
05

Safety considerations

Calculated index variabilityDependence on fasting state for triglyceridesPotential for misinterpretation in patients with extreme dyslipidemiaLack of universal clinical thresholds across different ethnic populations
06

Interacting drugs

Atorvastatin

8 more in the full profile.

07

Biomarkers

TriglyceridesHigh-density lipoprotein cholesterol (HDL-C)Small dense low-density lipoprotein (sdLDL)

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