Prevention & lipidsCross-sectional study

Lipoprotein(a) distributions and trial eligibility thresholds for Lp(a)-lowering therapies in the general population: the Rotterdam study

Eur J Prev CardiolPublished

  • Cross-sectional study
  • population-based

Authors' conclusion

Lp(a) distributions and MACE rates substantially vary across high-risk groups in the general population.

Study context

Population
Rotterdam Study participants, including high-risk groups (atherosclerotic cardiovascular disease (ASCVD), chronic kidney disease (CKD), subclinical atherosclerosis, calcific aortic valve disease)
Participants
5,129 participants
Exposure
ASCVD vs aortic valve calcification (AVC) score >300

Main finding

As reported in the abstract

Prevalence of Lp(a) above trial thresholds and NNS
GroupLp(a) >150 nmol/LLp(a) >200 nmol/LNumbers needed to screen (NNS) >150 nmol/LNNS >200 nmol/LNNS
ASCVD13.5% (11.9-15.3%)6.5% (5.3-7.8%)7.415.4
AVC score >30020.2% (13.0-27.4)11.8% (6.6-19.0)5.0-8.5

Observational data: associations, not effects.

Further findings

Major adverse cardiovascular event (MACE) rates

MACE rates varied by group and increased progressively with higher Lp(a) thresholds

Original publication

Lipoprotein(a) distributions and trial eligibility thresholds for Lp(a)-lowering therapies in the general population: the Rotterdam study. Eur J Prev Cardiol. Published 31 August 2026. doi:10.1093/eurjpc/zwag425

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