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Epidemiology

Lp(a) above 50 mg/dL confers over 10-fold higher risk of heart attack, stroke or amputation in patients with existing artery disease, the FRENA registry of 1503 patients (Atherosclerosis 2018)

Original title: Lipoprotein (a) levels and outcomes in stable outpatients with symptomatic artery disease

Atherosclerosis · · 8

Sanchez Muñoz-Torrero JF, Rico-Martín S, Álvarez LR, Aguilar E, Alcalá JN, Monreal M, FRENA Investigators

The FRENA registry, a prospective cohort of consecutive outpatients with coronary, cerebrovascular or peripheral artery disease, recruited 1503 stable patients as of December 2016, of whom 814 (54%) had Lp(a) below 30 mg/dL, 319 (21%) had 30-50 mg/dL, and 370 (25%) had 50 mg/dL or higher. Over a mean 36-month follow-up, 294 patients developed subsequent events (122 myocardial infarction, 114 ischemic stroke, 58 limb amputation) and 85 died. Patients with 30-50 mg/dL had higher risk of myocardial infarction (hazard ratio 4.67), ischemic stroke (hazard ratio 8.27) or limb amputation (hazard ratio 3.18) than those with normal levels, while those at 50 mg/dL or higher had far greater risk of myocardial infarction (hazard ratio 19.5), ischemic stroke (hazard ratio 54.5) or limb amputation (hazard ratio 22.7). The findings show Lp(a) above 30 mg/dL confers 5-fold higher risk and above 50 mg/dL over 10-fold higher risk of subsequent vascular events in patients with existing symptomatic artery disease.

Read the paper (DOI)PubMed

Original abstract

Background And Aims: Although genetic and epidemiological studies support that people with high lipoprotein (a) [Lp(a)] levels are at an increased risk for arterial disease, its prognostic value in patients with established artery disease has not been consistently evaluated.

Methods: FRENA is a prospective registry of consecutive outpatients with coronary, cerebrovascular or peripheral artery disease. We assessed the risk for subsequent myocardial infarction, ischemic stroke or limb amputation according to Lp(a) levels at baseline.

Results: As of December 2016, 1503 stable outpatients were recruited. Of these, 814 (54%) had levels <30 mg/dL, 319 (21%) had 30-50 mg/dL and 370 (25%) had ≥50 mg/dL. Over a mean follow-up of 36 months, 294 patients developed subsequent events (myocardial infarction 122, ischemic stroke 114, limb amputation 58) and 85 died. On multivariable analysis, patients with Lp(a) levels of 30-50 mg/dL were at a higher risk for myocardial infarction (hazard ratio [HR]: 4.67; 95%CI: 2.77-7.85), ischemic stroke (HR: 8.27; 95%CI: 4.14-16.5) or limb amputation (HR: 3.18; 95%CI: 1.36-7.44) than those with normal levels. Moreover, patients with levels ≥50 mg/dL were at increased risk for myocardial infarction (HR: 19.5; 95%CI: 10.5-36.1), ischemic stroke (HR: 54.5; 95%CI: 25.4-116.7) or limb amputation (HR: 22.7; 95%CI: 9.38-54.9).

Conclusions: Stable outpatients with symptomatic artery disease and Lp(a) levels >30 mg/dL were at a 5-fold higher risk for subsequent myocardial infarction, stroke or limb amputation. Those with levels >50 mg/dL were at an over 10-fold higher risk.

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