Prevention & lipidsCross-sectional study

Evaluating the role of lipoprotein(a) in enhancing risk stratification for the presence and extent of subclinical coronary artery disease burden: a BioHEART-CT study

Eur J Prev CardiolPublished

  • Cross-sectional study
  • Optimal threshold by Youden's index with 10,000 bootstraps

Authors' conclusion

Our findings suggest Lp(a)'s role in a new clinical pathway: screening patients considered low or intermediate risk, particularly those without standard modifiable risk factors for non-invasive imaging to detect subclinicalCAD.

Study context

Population
Adults undergoing CTCA for suspected CAD enrolled in the BioHEART study
Participants
1,718 adults
Exposure
Lp levels and CT measures of subclinical CAD burden
Outcome
CAD burden by CACS and Gensini scores; plaque morphology (calcified, non-calcified or mixed)

Main finding

As reported in the abstract

Association of Lp(a) with CTCA measures of CAD
Lp(a) >22 nmol/LOrdinal OR (CI)
more advanced multi-segment disease
1.14(1.03–1.25)
multivessel disease
1.11(1.02–1.20)
Increased risk of coronary artery calcium score (CACS) >100 per 10 nmol/L Lp(a) increment
2.6%
Association with mixed plaque burden, adjusted for traditional risk factors (not with non-calcified or calcified plaque)
β = 4.75, p=0.001
Overall NRI adding Lp(a) to standard risk models
16% [0.06-0.27]
NRI in patients without standard modifiable risk factors
42% [0.16-0.70]

Observational data: associations, not effects.

Further findings

Reclassification adding Lp(a) to standard risk models

Overall NRI
16% [0.06-0.27]
NRI in patients without standard modifiable risk factors
42% [0.16-0.70]

Original publication

Evaluating the role of lipoprotein(a) in enhancing risk stratification for the presence and extent of subclinical coronary artery disease burden: a BioHEART-CT study. Eur J Prev Cardiol. Published 3 June 2025. doi:10.1093/eurjpc/zwaf323

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