Abstract 4358554: Coronary Artery Calcium Predicts All-cause and Non-coronary Mortality
Abstract
Background: Coronary artery calcium (CAC) is a strong predictor of coronary artery disease (CAD) risk, and CAC=0 is a highly favorable prognostic marker. Recently, the prognostic value of CAC has been proposed to extend to all-cause and non-coronary mortality. For example, CAC is a predictor of calcification in other vascular beds, and CAD is reported to impact immune surveillance and cancer risk. Methods: We tested whether CAC can predict the risk of total mortality (TM), and we estimated whether cause-specific and non-coronary mortality distributions are impacted by CAC. We searched the Intermountain Health electronic medical records (eMR) database for patients (pts) at primary coronary risk who underwent positron emission tomography/computed tomography (PET/CT) stress testing and had a 5y follow-up. We compared unadjusted and age/sex-adjusted TM rates between CAC=0 and CAC>0 pts. We determined cause-specific mortality proportions for all CAC=0 pts and estimated these from a 1:10 random sample of CAC>0 pts by chart review. We examined proportions of 5y cause-specific deaths in CAC=0 pts and explored differences with CAC>0 patients. Results: The eMR search identified 40,018 pts undergoing PET/CT who were at primary coronary risk. Mean age was 65.8 [11.9] y; 48.7% were female; 7967 (19.9%) had CAC=0 by CT; and 32,051 were CAC>0. There were 238 deaths (2.99%) in CAC=0 and 2834 (8.84%) in CAC>0 cohort, for a relative risk (RR) of 0.34 (p<0.001). In age and sex adjusted logistic regression, CAC>0 remained a highly significant risk factor (OR=2.04, p<0.0001; Table 1). Distributions of cause-specific deaths are shown in Table 2 by CAC category. CAC=0 predicted a very low proportion of CAD-related and total cardiovascular (CV) deaths. Most of the greater rate of TM in CAC>0 patients was estimated to be non-CV. Conclusions: In this large, integrated healthcare system experience, a zero CAC score predicted an excellent prognosis for TM, with CAC>0 being associated with a >2-fold greater TM risk than CAC=0. Further, CAC=0 was associated with a very low proportion of both CAD-related and all CV mortality. Most of CAC>0 TM was estimated to be non-CV. The implications of a zero CAC score may go beyond simply marking a low risk of CAD-related events to also being a marker of general vascular health and improved overall survival.
Article Details
Authors (9)
Jeffrey Anderson
Dave Collingridge
INTERMOUNTAIN MEDICAL CENTER, Murray, Utah, United States
Stacey Knight
Viet Le
INTERMOUNTAIN MEDICAL CENTER, Salt Lake City, Utah, United States
Leslie Iverson
INTERMOUNTAIN MEDICAL CENTER, Salt Lake City, Utah, United States
Tami Bair
Intermountain Medical Center, Salt Lake Cty, Utah, United States
Steve Mason
Intermountain Medical Center Heart Institute, Intermountain Healthcare, Murray, UT; Department of Internal Medicine, University of Utah, Salt Lake City, UT (S.K., V.T.L., S.M.).
Joseph Muhlestein
Intermountain Medical Center Heart Institute, Murray, Utah, United States
Kirk Knowlton
Intermountain Medical Center Heart Institute, Murray, Utah, United States