Abstract 4366598: Comparative Performance of PCE, PREVENT, and CAC for MACE Prediction in Asymptomatic Patients

G Gabrielle Gershon (Emory University, Atlanta, Georgia, United States) J Jaret Barr (Emory University, Atlanta, Georgia) M Martin Halicek (Emory University, Atlanta, Georgia, United States) Y Yan Yang E Eshan Momin (Emory University, Atlanta, Georgia, United States) A Alexander Razavi (Emory University School of Medicine, Atlanta, Georgia, United States) O Omar Dzaye (JOHNS HOPKINS UNIVERSITY, Baltimore, Maryland, United States) S Seamus Whelton (Johns Hopkins School of Medicine, Baltimore, Maryland, United States) M Michael Blaha (JOHNS HOPKINS HOSPITAL, Baltimore, Maryland, United States) R Roger Blumenthal (Johns Hopkins University School of Medicine, Baltimore, Maryland, United States) L Laurence Sperling C Carlo De Cecco (Emory University, Atlanta, Georgia, United States) M Marly van Assen

Abstract

Introduction/Background: Current prediction models including the Pooled Cohort Equations (PCE) and the novel PREVENT score are used for assessing atherosclerotic cardiovascular disease (ASCVD) risk. Coronary artery calcium (CAC) scoring can further refine risk stratification, but its integration with PREVENT remains unknown. Research Questions/Hypothesis: How does the performance of PCE, PREVENT, and CAC—individually and combined— compare for predicting Major Adverse Cardiac Events (MACE) in asymptomatic adults? Methods/Approach: Among 14,570 asymptomatic patients from the Emory CAC Registry (2010–2023), PCE and PREVENT 10-year risk scores were calculated, and CAC was quantified via Agatston scoring using a validated AI method. MACE (myocardial infarction, stroke, revascularization>90 days) was ascertained via ICD/CPT codes. Kaplan-Meier survival curves and Cox proportional hazard ratios were used to evaluate MACE across stratified risk groups. Discrimination was assessed using Harrell’s C-statistic across PCE risk strata (0–2.5%, 2.5-5%, 5-7.5%, 7.5-10%, 10-20% and >20%). Results/Data: The mean age was 56.5 years, 42% were women, 78% were white. Median CACS was 1.3 (IQR 0,49) (44% had CAC = 0). Mean PCE was 7% and mean ASCVD PREVENT was 4%. PREVENT alone outperformed PCE alone (C-statistic 0.64 vs. 0.59, p<0.01), with higher hazard ratios for increasing risk groups (5-7.5% risk: PCE HR 1.7 vs PREVENT HR 2.1 and 10-20% risk: PCE HR 2.8 vs PREVENT HR 4 (vs 0-2.5% risk group)). CAC showed a graded association with MACE (CAC >300: HR=3.8, p<0.001 vs CAC=0). Across all risk strata groups, adding CAC to PCE and PREVENT improved discrimination, with the most substantial improvement in PCE risk groups 2.5-5% and 10-20% (Δ C-statistic =+0.1 for both). Sex-based differences in model performance existed (C-statistics of 0.57-0.74 in men versus 0.57-0.59 in women). Conclusion(s): CAC further enhances MACE risk discrimination with PCE and PREVENT, particularly in intermediate-risk groups and in males. Integrating CAC with PREVENT may assist in optimizing primary prevention strategies.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (13)

G

Gabrielle Gershon

Emory University, Atlanta, Georgia, United States

J

Jaret Barr

Emory University, Atlanta, Georgia

M

Martin Halicek

Emory University, Atlanta, Georgia, United States

Y

Yan Yang

E

Eshan Momin

Emory University, Atlanta, Georgia, United States

A

Alexander Razavi

Emory University School of Medicine, Atlanta, Georgia, United States

O

Omar Dzaye

JOHNS HOPKINS UNIVERSITY, Baltimore, Maryland, United States

S

Seamus Whelton

Johns Hopkins School of Medicine, Baltimore, Maryland, United States

M

Michael Blaha

JOHNS HOPKINS HOSPITAL, Baltimore, Maryland, United States

R

Roger Blumenthal

Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

L

Laurence Sperling

C

Carlo De Cecco

Emory University, Atlanta, Georgia, United States

M

Marly van Assen