Prevention & lipids

Elevated apolipoprotein B (apoB) due to high remnant cholesterol confers high risk of atherosclerotic cardiovascular disease (ASCVD) without prompting sufficient lipid-lowering therapy: a guideline-based limitation and an unmet medical need

Eur J Prev CardiolPublished Prospective cohort study

Authors' conclusion

In a primary prevention setting, elevated apoB due to high remnant cholesterol confers high risk of ASCVD but less initiation of lipid-lowering therapy compared to elevated apoB due to high LDL cholesterol, representing a guideline-based limitation and an unmet medical need.

Study context

Population
Lipid-lowering therapy naïve adults without a history of ASCVD, Copenhagen General Population Study, 2003–20159,269 developed ASCVD
Participants
94,299 adults
Exposure
Elevated apoB due to high remnant cholesterol vs elevated apoB due to high LDL-C, each vs concordant low values
Outcome
Incident ASCVD and initiation of lipid-lowering therapy
Follow-up
Median 12 years
Methodological detailsgeneral population cohort, discordance analysis
  • General population cohort
  • Discordance analysis

Main finding

As reported in the abstract

Estimate
High remnant cholesterol and high apoB, low LDL-C vs Concordant lowASCVD
HR 1.45(95% CI 1.34–1.56)
High remnant cholesterol and high apoB, low LDL-C vs Concordant lowstarting lipid-lowering therapy within one year
OR 3.0(CI 2.5–3.6)
Low remnant cholesterol, high apoB and high LDL-C vs Concordant lowASCVD
HR 1.20(CI 1.11–1.30)
Low remnant cholesterol, high apoB and high LDL-C vs Concordant lowstarting lipid-lowering therapy
OR 5.1(CI 4.3–5.9)

Observational data: associations, not effects.

Original publication

Elevated apoB due to high remnant cholesterol confers high risk of ASCVD without prompting sufficient lipid-lowering therapy: a guideline-based limitation and an unmet medical need. Eur J Prev Cardiol. Published 5 December 2025. doi:10.1093/eurjpc/zwaf735

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

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.