A focused update to the 2019 NLA scientific statement on use of lipoprotein(a) in clinical practice

Elsevier

Available online 1 April 2024

Journal of Clinical LipidologyAuthor links open overlay panel, , , , , , , , , , , , , , Highlights•

Lp(a) level should be measured at least once in all adults.

Lp(a) levels represent a continuum of risk, not a risk threshold at a dichotomous cutpoint.

Risk classification by Lp(a) level ranges from low (<75 nmol/L) to high (≥125 nmol/L).

Lp(a) risk categories apply across races and ethnicities.

High Lp(a) levels warrant early and more-intensive risk factor management.

Since the 2019 National Lipid Association (NLA) Scientific Statement on Use of Lipoprotein(a) in Clinical Practice was issued, accumulating epidemiological data have clarified the relationship between lipoprotein(a) [Lp(a)] level and cardiovascular disease risk and risk reduction. Therefore, the NLA developed this focused update to guide clinicians in applying this emerging evidence in clinical practice. We now have sufficient evidence to support the recommendation to measure Lp(a) levels at least once in every adult for risk stratification. Individuals with Lp(a) levels <75 nmol/L (30 mg/dL) are considered low risk, individuals with Lp(a) levels ≥125 nmol/L (50 mg/dL) are considered high risk, and individuals with Lp(a) levels between 75 and 125 nmol/L (30–50 mg/dL) are at intermediate risk. Cascade screening of first-degree relatives of patients with elevated Lp(a) can identify additional individuals at risk who require intervention. Patients with elevated Lp(a) should receive early, more-intensive risk factor management, including lifestyle modification and lipid-lowering drug therapy in high-risk individuals, primarily to reduce low-density lipoprotein cholesterol (LDL-C) levels. The U.S. Food and Drug Administration approved an indication for lipoprotein apheresis (which reduces both Lp(a) and LDL-C) in high-risk patients with familial hypercholesterolemia and documented coronary or peripheral artery disease whose Lp(a) level remains ≥60 mg/dL [∼150 nmol/L)] and LDL-C ≥ 100 mg/dL on maximally tolerated lipid-lowering therapy. Although Lp(a) is an established independent causal risk factor for cardiovascular disease, and despite the high prevalence of Lp(a) elevation (∼1 of 5 individuals), measurement rates are low, warranting improved screening strategies for cardiovascular disease prevention.

Keywords

Lipoprotein(a)

Cardiovascular disease

Risk assessment

Treatment practice

Guidelines

Prevention

Scientific statements

View Abstract

© 2024 National Lipid Association. Published by Elsevier Inc. All rights reserved.

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