Abstract 4363281: Mitral Annular Calcification, Coronary Artery Calcification, and Risk of Incident Atrial Fibrillation in the Multi-Ethnic Study of Atherosclerosis (MESA)

P Parag Chevli (Wake Forest University School of Medicine, Winston Salem, North Carolina, United States) S Soroush Masrouri (Shahid Beheshti University of Medical Sciences, Tehran, Iran (the Islamic Republic of)) A Alexander Razavi (Emory University School of Medicine, Atlanta, Georgia, United States) T Takeki Suzuki (Wake Forest School of Medicine, Winston-Salem, North Carolina, United States) J Joseph Yeboah (WAKE FOREST UNIVERSITY, Winston Salem, North Carolina, United States) N Natalie Bradford (Wake Forest University, Winston Salem, North Carolina, United States) S Susan Heckbert (UNIVERSITY OF WASHINGTON, Seattle, Washington, United States) E Elsayed Soliman (Wake Forest School of Medicine, Winston-Salem, North Carolina, United States) M Michael Shapiro (Wake Forest Univ School of Medicine, Winston Salem, North Carolina, United States) P Prashant Bhave (Wake Forest School of Medicine, Winston Salem, North Carolina, United States)

Abstract

Background: Atrial fibrillation (AF) is a prevalent arrhythmia associated with significant morbidity and mortality. Coronary artery calcification (CAC) and mitral annular calcification (MAC) are markers of cardiovascular aging and systemic atherosclerosis, but data on their joint association with incident AF are limited. We investigated the independent and combined associations of CAC and MAC with incident AF in the Multi-Ethnic Study of Atherosclerosis (MESA) to assess potential synergistic effects and elucidate the mechanisms linking cardiovascular calcification to AF. Hypothesis: We hypothesized that CAC and MAC are independently associated with increased AF risk, and that their combination confers additive risk beyond traditional predictors. Methods: CAC and MAC were assessed by cardiac CT and quantified by Agatston scoring. Participants were stratified into four groups: CAC=0/MAC=0 (reference), CAC>0/MAC=0, CAC=0/MAC>0 and CAC>0/MAC>0. Incident AF was ascertained through hospitalization and medical records as well as Medicare claims. Cox proportional hazard models were used to examine the association between CAC/MAC categories and incident AF, adjusting for demographics (Model 2) and cardiovascular risk factors (Model 3), with model 1 unadjusted. We used Harrell’s C-statistic to assess model performance with the incremental addition of CAC and MAC to the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE)-AF risk score. Results: We included 6,588 MESA participants (mean age 62±10 years, 53% female) free of baseline AF and cardiovascular disease. Over a median follow-up of 16.5 years, 1,306 incident AF events occurred. Participants with CAC>0/MAC>0 were at the highest risk of incident AF ( Image 1 ). In the fully adjusted model, compared to those in the reference group (CAC=0/MAC=0), participants with CAC>0/MAC=0, CAC=0/MAC>0, and CAC>0/MAC>0 demonstrated a 39%, 74%, and 96% increased risk of incident AF events, respectively (p<0.01 for all) ( Image 2 ). Addition of CAC and MAC to the CHARGE-AF model significantly improved risk discrimination (C-statistic improved from 0.746 to 0.754, p<0.001). Conclusions: Both CAC and MAC are independently associated with increased risk of incident AF. Their combination identifies individuals at even higher risk and improves predictive performance when added to the CHARGE-AF model. These findings suggest that cardiac CT-derived calcification measures may enhance AF risk stratification.

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 (10)

P

Parag Chevli

Wake Forest University School of Medicine, Winston Salem, North Carolina, United States

S

Soroush Masrouri

Shahid Beheshti University of Medical Sciences, Tehran, Iran (the Islamic Republic of)

A

Alexander Razavi

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

T

Takeki Suzuki

Wake Forest School of Medicine, Winston-Salem, North Carolina, United States

J

Joseph Yeboah

WAKE FOREST UNIVERSITY, Winston Salem, North Carolina, United States

N

Natalie Bradford

Wake Forest University, Winston Salem, North Carolina, United States

S

Susan Heckbert

UNIVERSITY OF WASHINGTON, Seattle, Washington, United States

E

Elsayed Soliman

Wake Forest School of Medicine, Winston-Salem, North Carolina, United States

M

Michael Shapiro

Wake Forest Univ School of Medicine, Winston Salem, North Carolina, United States

P

Prashant Bhave

Wake Forest School of Medicine, Winston Salem, North Carolina, United States