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Aortic stenosis

High Lp(a) affects 10-20% of the population and up to 1 billion people worldwide, tripling risk of aortic stenosis and peripheral artery disease, a review (Clin Chem 2021)

Original title: Lipoprotein(a) and Cardiovascular Disease

Clin Chem · · 6

Kamstrup PR

This review by Kamstrup summarises evidence for Lp(a) as a causal driver of cardiovascular disease. High Lp(a), present in 10%-20% of the population and an estimated more than 1 billion people worldwide, is supported as causal by mechanistic, observational and genetic studies across coronary heart disease, peripheral arterial disease, aortic valve stenosis, and likely ischaemic stroke. Effect sizes are most pronounced for myocardial infarction, peripheral arterial disease and aortic valve stenosis, where high Lp(a) predicts 2- to 3-fold increased risk. The author calls for Lp(a) measurement using well-validated, calibrator-traceable assays to ensure consistent risk cut-offs, and for randomised cardiovascular outcome trials to provide final proof of causality and assess the clinical benefit of emerging potent Lp(a)-lowering therapies.

Read the paper (DOI)PubMed

Original abstract

Background: High lipoprotein(a) concentrations present in 10%-20% of the population have long been linked to increased risk of ischemic cardiovascular disease. It is unclear whether high concentrations represent an unmet medical need. Lipoprotein(a) is currently not a target for treatment to prevent cardiovascular disease.

Content: The present review summarizes evidence of causality for high lipoprotein(a) concentrations gained from large genetic epidemiologic studies and discusses measurements of lipoprotein(a) and future treatment options for high values found in an estimated >1 billion individuals worldwide.

Summary: Evidence from mechanistic, observational, and genetic studies support a causal role of lipoprotein(a) in the development of cardiovascular disease, including coronary heart disease and peripheral arterial disease, as well as aortic valve stenosis, and likely also ischemic stroke. Effect sizes are most pronounced for myocardial infarction, peripheral arterial disease, and aortic valve stenosis where high lipoprotein(a) concentrations predict 2- to 3-fold increases in risk. Lipoprotein(a) measurements should be performed using well-validated assays with traceability to a recognized calibrator to ensure common cut-offs for high concentrations and risk assessment. Randomized cardiovascular outcome trials are needed to provide final evidence of causality and to assess the potential clinical benefit of novel, potent lipoprotein(a) lowering therapies.

aortic stenosisgeneticsrisk prediction

Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.