Comparative effectiveness of atorvastatin monotherapy vs. atorvastatin plus bempedoic acid combination in patients

Laith Rhabneh1, Ra'ed Ababneh1, Ibrahim Alnaser2

  • 1INTERNAL MEDICINE DEPARTMENT, HACKENSACK MERIDIAN OCEAN UNIVERSITY MEDICAL CENTER, BRICK TOWNSHIP, UNITED STATES.

Insights

Adding bempedoic acid to atorvastatin therapy significantly reduces major adverse cardiovascular events (MACE), cardiac arrest, and hospitalizations in coronary artery disease (CAD) patients. This combination therapy demonstrated a protective effect without increasing the risk of myopathy.

Area of Science:

  • Cardiovascular Medicine
  • Pharmacology
  • Clinical Research

Background:

  • Established coronary artery disease (CAD) necessitates effective lipid-lowering strategies.
  • Atorvastatin is a common treatment, but additional therapies may be required to optimize cardiovascular outcomes.
  • The role of bempedoic acid in combination with statins warrants investigation for enhanced cardiovascular protection.

Purpose of the Study:

  • To evaluate the impact of adding bempedoic acid to atorvastatin therapy on cardiovascular outcomes.
  • To assess the effect on major adverse cardiovascular events (MACE), cardiac arrest, and all-cause hospitalization.
  • To determine the incidence of myopathy in patients receiving combination therapy versus atorvastatin monotherapy.

Main Methods:

  • A retrospective cohort study utilizing the TriNetX global health research network.
  • Patients with established CAD were divided into atorvastatin monotherapy and atorvastatin plus bempedoic acid cohorts.
  • Propensity score matching was used to ensure balanced baseline characteristics between the two groups.

Main Results:

  • The combination therapy group (atorvastatin + bempedoic acid) showed a significantly lower incidence of MACE (3.2% vs. 5.7%).
  • Hazard ratios indicated reduced risk for cardiac arrest (HR 1.628) and all-cause hospitalizations (HR 1.418) with combination therapy.
  • No significant difference in the incidence of myopathy was observed between the atorvastatin monotherapy and combination therapy groups.

Conclusions:

  • Adding bempedoic acid to atorvastatin therapy provides a significant protective effect against major adverse cardiovascular events in CAD patients.
  • The combination therapy reduces cardiac arrest and hospitalizations without a statistically significant increase in myopathy.
  • Further prospective studies are recommended to validate these findings on cardiovascular outcomes.
Abstract

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