Publication

Long-term all-cause and cause-specific mortality in asymptomatic patients with CAC ≥ 1000: Results from the Coronary Artery Calcium Consortium

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Last modified
  • 05/20/2025
Type of Material
Authors
    Allison W. Peng, Johns Hopkins UniversityMohammadhassan Mirbolouk, Johns Hopkins UniversityOlusola A. Orimoloye, Johns Hopkins UniversityAlbert D. Osei, Johns Hopkins UniversityZeina Dardari, Johns Hopkins UniversityOmar Dzaye, Johns Hopkins UniversityMatthew J. Budoff, Harbor-UCLA Medical CenterLeslee Shaw, Emory UniversityMichael D. Miedema, Minneapolis Heart InstituteJohn Rumberger, Princeton Longevity CenterDaniel S. Berman, Cedars-Sinai Medical CenterAlan Rozanski, Mount Sinai School of MedicineMouaz H. Al-Mallah, Houston Methodist HospitalKhurram Nasir, Yale UniversityMichael J. Blaha, Johns Hopkins University
Language
  • English
Date
  • 2020-01-01
Publisher
  • Elsevier
Publication Version
Copyright Statement
  • © 2020 by the American College of Cardiology Foundation. Published by Elsevier.
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 13
Issue
  • 1 Pt 1
Start Page
  • 83
End Page
  • 93
Grant/Funding Information
  • MJB is supported by NIH/NHLBI L30 HL110027. There are no financial disclosures to support.
Supplemental Material (URL)
Abstract
  • Objectives We thoroughly explored the demographic and imaging characteristics, as well as all-cause and cause-specific mortality of CAC≥1000 patients in the largest dataset of this population to date. Background Coronary artery calcium (CAC) is commonly used to quantify cardiovascular risk. Current guidelines classify CAC>300 or 400 as the highest risk group, yet little is known about the potentially unique imaging characteristics and mortality risk in individuals with CAC≥1000. Methods We included 66,636 asymptomatic adults from the CAC Consortium, a large retrospective multicenter clinical cohort. Mean patient follow-up was 12.3 ± 3.9 years for CVD, CHD, cancer, and all-cause mortality. Using multivariable Cox proportional hazards regression models adjusted for age, sex, and traditional risk factors, we assessed the relative mortality hazard of individuals with CAC≥1000 compared first against a reference of CAC=0, and then against CAC 400–999. Results There were 2,869 patients with CAC≥1000 (86.3% male, mean age 66.3 ± 9.7 years). Most CAC≥1000 patients had 4-vessel CAC (mean 3.5 ± 0.6 vessels), and had greater total CAC area, higher mean CAC density, and more extra-coronary calcium (79% with TAC, 46% with AVC, 21% with MVC) compared to CAC 400–999. After full adjustment, those with CAC≥1000 had 5.04 (3.92–6.48), 6.79 (4.74–9.73), 1.55 (1.23–1.95), and 2.89-fold (2.53–3.31) risk of CVD, CHD, cancer, and all-cause mortality, respectively, compared to those with CAC=0. The CAC≥1000 group had a 1.71- (1.41–2.08), 1.84- (1.43–2.36), 1.36- (1.07–1.73), and 1.51-fold (1.33–1.70) increased CVD, CHD, cancer, and all-cause mortality compared to CAC 400–999. Graphical analysis of CAC≥1000 revealed continued logarithmic increase in risk, with no clear evidence of a risk plateau. Conclusions Patients with extensive CAC (CAC≥1000) represent a unique very high-risk phenotype with mortality outcomes commensurate with high-risk secondary prevention patients. Future guidelines should consider CAC≥1000 a distinct risk group which may benefit from the most aggressive preventive therapy.
Author Notes
  • Correspondence: Michael J. Blaha, MD, MPH, Director of Clinical Research, Ciccarone Center for the Prevention of Heart Disease, Associate Professor of Medicine, Blalock 524D1, 600 N. Wolfe Street, Baltimore, MD 21287, mblaha1@jhmi.edu, Phone: 410-955-7376, Fax: 410-614-9190
Keywords
Research Categories
  • Health Sciences, Medicine and Surgery
  • Health Sciences, Health Care Management
  • Health Sciences, Pathology

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