Prevention & lipidsSecondary analysis

Lipoprotein(a) Blood Levels and Cardiovascular Risk Reduction With Icosapent Ethyl

J Am Coll CardiolPublished

  • Post hoc analysis of the REDUCE-IT randomised trial

Authors' conclusion

Baseline Lp(a) concentration was prognostic for MACE among participants with elevated triglyceride levels receiving statin therapy. Importantly, IPE consistently reduced MACE across a range of Lp(a) levels, including among those with clinically relevant elevations.

Study context

Population
Statin-treated patients with established CVD or age ≥50 years with DM and ≥1 additional risk factor, fasting TG 1.69 to 5.63 mmol/L, LDL-C 1.06 to 2.59 mmol/L7,026 with baseline Lp(a)
Participants
8,179 patients
Comparison
Icosapent ethyl (IPE) vs placebo across Lp levels
Primary endpoint
First MACE by baseline Lp(a) (≥50 or <50 mg/dL); relationship of continuous Lp(a) with first and total MACE

Primary result

As reported in the abstract

MACE by Lp(a) level

Event reductions with IPE did not vary across the range of Lp(a)

interaction P > 0.10

Lp(a) significantly related to first and total major adverse cardiovascular events (MACE)

P < 0.0001

Further findings

Baseline Lp(a) concentration

Median Lp(a), mg/dL (Q1-Q3: 5.0-37.4)
11.6
  • 7,026 participants with baseline Lp(a)

Original publication

Lipoprotein(a) Blood Levels and Cardiovascular Risk Reduction With Icosapent Ethyl. J Am Coll Cardiol. Published 25 March 2024. doi:10.1016/j.jacc.2024.02.016

Summarised from the published abstract; every number is checked against it