Prevention & lipids

Integrating cardiac biomarkers into the AHA PREVENT equations: impact on atherosclerotic cardiovascular disease risk stratification

Eur Heart J Qual Care Clin OutcomesPublished Pooled cohort analysis with external validation

Authors' conclusion

Integrating cardiac biomarkers into PREVENT equations identifies high-risk individuals masked by traditional factors, optimizing the clinical yield of primary prevention, especially for borderline-risk populations.

Study context

Population
Atherosclerotic cardiovascular disease (ASCVD)-free participants (primary prevention)pooled primary cohort (mean age 62.0 years, 55.9% female), external validation in UK Biobank (UKB) · Primary cohort (ARIC and MESA) 15,477 · UK Biobank (UKB) external validation 40,359
Participants
15,477 participants
Comparison
Biomarker-augmented PREVENT model vs PREVENT equations
Outcome
ASCVD events
Follow-up
median 12.1-year follow-up
Methodological detailsAtherosclerosis Risk in Communities and Multi-Ethnic Study of Atherosclerosis cohorts pooled, external validation in UK Biobank (UKB)
  • Atherosclerosis Risk in Communities and Multi-Ethnic Study of Atherosclerosis cohorts pooled
  • External validation in UK Biobank (UKB)

Performance

As reported in the abstract

Events in primary cohort

1836

Further findings

ASCVD events by clinical risk and biomarker category

HR (95% CI)
Clinical low/borderline risk with elevated biomarkersReference group not stated2.74 (2.45–3.06)
High clinical risk with normal biomarkersReference group not stated1.42 (1.22–1.65)
Combined high-risk groupHighest risk; reference group not stated4.46 (3.92–5.07)

Reclassification into the intermediate-risk category (≥7.5%) by incorporating biomarkers

Low-risk (<5%) individuals reclassified
16.4%
Borderline-risk (5-7.5%) individuals reclassified
25.8%

Performance of the biomarker-augmented PREVENT model

ΔC-index
0.022; P < 0.001
Net reclassification improvement (NRI)
0.193
Integrated discrimination improvement (IDI)
0.102
Well-calibrated
Reclassification improvement highest in the borderline-risk group

Decision curve analysis at the 7.5% clinical threshold

Increase in net benefit
three-fold
Additional true-positive cases per 1000 individuals, without increasing over-treatment
27

External validation in UKB, borderline-risk group

ΔAUC
0.049; P < 0.001
  • Findings robustly confirmed in UKB; borderline-risk group showed the highest improvement

Original publication

Integrating cardiac biomarkers into the AHA PREVENT equations: impact on atherosclerotic cardiovascular disease risk stratification. Eur Heart J Qual Care Clin Outcomes. Published 26 February 2026. doi:10.1093/ehjqcco/qcag025

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