Evaluation of lipid-lowering therapy in patients with elevated lipoprotein(a) levels

Michael S Kelly1, Ruth N Jeminiwa1, Fatima Gohar1

  • 1Thomas Jefferson University College of Pharmacy, Jefferson College of Pharmacy, Philadelphia, PA, USA (Drs Kelly, and Jeminiwa; Gohar, Fanous, and Ramirez).

PubMed

Insights

Less than a quarter of patients with high lipoprotein(a) (Lp(a)) had their lipid-lowering therapy intensified. Elevated LDL-C predicted medication changes, but further research is needed on Lp(a)-lowering strategies.

Area of Science:

  • Cardiology
  • Clinical Lipidology
  • Pharmacotherapy

Background:

  • Elevated lipoprotein(a) (Lp(a)) is a key independent risk factor for atherosclerotic cardiovascular disease (ASCVD).
  • Managing modifiable ASCVD risk factors like hypertension and dyslipidemia is crucial for patients with high Lp(a).
  • Current clinical practices for modifying lipid-lowering therapy in response to elevated Lp(a) are not well-documented.

Purpose of the Study:

  • To analyze changes in lipid-lowering therapy among patients with elevated Lp(a).
  • To identify patient characteristics associated with the intensification of lipid-lowering medications.

Main Methods:

  • Retrospective, observational case-control study design.
  • Analysis of lipid-lowering therapy modifications in patients with Lp(a) ≥ 30 mg/dL (75 nmol/L).
  • Data collected from January 1, 2020, to May 31, 2024.

Main Results:

  • Out of 539 eligible patients, 120 (22.3%) experienced therapy modification within 30 days of an elevated Lp(a) result.
  • The most frequent interventions included adding ezetimibe (33.3%) and intensifying statin therapy (32.5%).
  • Elevated low-density lipoprotein cholesterol (LDL-C) was the strongest predictor for lipid medication changes.

Conclusions:

  • Lipid-lowering medication intensification occurred in less than 25% of patients with elevated Lp(a) within 30 days.
  • Further research is required to compare the efficacy of aggressive LDL-C lowering versus Lp(a)-lowering for ASCVD prevention in this patient group.
Abstract

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