Abstract 4370976: Redefining Risk: Enhancing Prognostic Assessment in Primary Prevention with Coronary Artery Calcium Score

S Sanmit Jindal (Houston Methodist, Houston, Texas, United States) I Izza Shahid (Houston Methodist Academic Institut, Houston, Texas, United States) A Aditya Siddharth (Houston Methodist Hospital, Houston, Texas, United States) R Rakesh Gullapelli (Houston Methodist, HOUSTON, Texas, United States) Z Zulqarnain Javed (Houston Methodist, Houston, Texas, United States) M Mahmoud Al Rifai (Houston Methodist, Houston, Texas, United States) S Sadeer Al-Kindi K Khurram Nasir

Abstract

Introduction: Current CV prevention strategies focus on treating individuals based on estimated risk or clinical thresholds, but risk heterogeneity exists even within treatment-eligible groups. Coronary artery calcium (CAC) scoring may enhance risk assessment, but its added value across the entire risk spectrum remains uncertain. Using data from a multiethnic population-based cohort, we examined the association of CAC burden with major adverse cardiovascular events (MACE). Methods: Adults aged 45–64 years without baseline ASCVD from the Multi-Ethnic Study of Atherosclerosis (MESA) were included. Participants were categorized into three mutually exclusive risk groups based on baseline pooled cohort equation (PCE) scores, LDL, systolic blood pressure (SBP), and diabetes status: therapy eligible intermediate-risk primary prevention, therapy eligible high-risk primary prevention, and therapy ineligible primordial prevention. CAC was categorized as 0, 1-<100, and ≥100 Agatston units. Cox proportional hazards models were used to assess the association between CAC categories and incident MACE across risk groups, adjusting for age, sex, race, body mass index (BMI), HDL cholesterol, triglycerides, and estimated glomerular filtration rate (eGFR). MACE was defined as a composite of hard CVD events, coronary revascularization, and cardiovascular death. Results: The cohort included 3,578 adults (mean age 54.6 years; 52.9% female; 27.6% African American), with a mean follow-up of 12.8 years. In fully adjusted models, higher CAC was independently associated with increased MACE risk across all risk groups. In the therapy eligible high-risk group, compared to CAC=0, the hazard ratio (HR) for CAC 1-99 was 2.22 (95% CI: 1.32-3.73; p=0.003) and 3.88 (95% CI: 2.31-6.50; p<0.001) for CAC ≥100. In the therapy eligible primary prevention group, HRs were 1.37 (95% CI: 0.85-2.19; p=0.191) for CAC 1-99 and 3.80 (95% CI: 2.40-6.04; p<0.0001) for CAC ≥100 ( Table 1 ). In the therapy ineligible primordial prevention group, HRs were 2.25 (95% CI: 1.41-3.61; p=0.001) for CAC 1–99 and 5.38 (95% CI: 3.14-9.21; p<0.0001) for CAC ≥100. Conclusion: Among treatment-eligible and ineligible adults, CAC provided independent and incremental prognostic information for MACE risk across the risk spectrum. These findings support the potential role of CAC testing to further individualize preventive strategies beyond traditional risk scores in both lower and higher risk populations.

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 (8)

S

Sanmit Jindal

Houston Methodist, Houston, Texas, United States

I

Izza Shahid

Houston Methodist Academic Institut, Houston, Texas, United States

A

Aditya Siddharth

Houston Methodist Hospital, Houston, Texas, United States

R

Rakesh Gullapelli

Houston Methodist, HOUSTON, Texas, United States

Z

Zulqarnain Javed

Houston Methodist, Houston, Texas, United States

M

Mahmoud Al Rifai

Houston Methodist, Houston, Texas, United States

S

Sadeer Al-Kindi

K

Khurram Nasir