TY - JOUR
T1 - Coronary artery Calcium predicts Cardiovascular events in participants with a low lifetime risk of Cardiovascular disease
T2 - The Multi-Ethnic Study of Atherosclerosis (MESA)
AU - Joshi, Parag H.
AU - Patel, Birju
AU - Blaha, Michael J.
AU - Berry, Jarett D.
AU - Blankstein, Ron
AU - Budoff, Matthew J.
AU - Wong, Nathan
AU - Agatston, Arthur
AU - Blumenthal, Roger S.
AU - Nasir, Khurram
N1 - Funding Information:
This work was supported by the National Heart, Lung, and Blood Institute at the National Institutes of Health [contracts N01-HC-95159 through N01-HC-95169] and the National Center of Research Resources at the National Institutes of Health [grants UL1-RR-024156 and UL1-RR-025005] to the MESA investigators and a National Institutes of Health training grant [T32HL007227] and the Pollin Cardiovascular Prevention Fellowship to PHJ.
Funding Information:
The authors would like to thank Zeina Dardari for her assistance with adapting the CVD risk calculator for analysis. The authors thank the other investigators, the staff, and the participants of the MESA study for their valuable contributions. A full list of participating MESA investigators and institutions can be found at http://www.mesa-nhlbi.org.
Publisher Copyright:
© 2016.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Aims: Patients with a low lifetime risk of coronary heart disease (CHD) are not completely free of events over 10 years. We evaluated predictors for CHD among "low lifetime risk" participants in the population-based Multi-Ethnic Study of Atherosclerosis (MESA). Methods: MESA enrolled 6814 men and women aged 45-84 years who were free of baseline cardiovascular disease. Using established criteria of non-diabetic, non-smokers with total cholesterol ≤200 mg/dL, systolic BP ≤ 139 mmHg, and diastolic BP ≤ 89 mmHg at baseline, we identified 1391 participants with a low lifetime risk for cardiovascular disease. Baseline covariates were age, gender, ethnicity, HDL-C, C-reactive protein, family history of CHD, carotid intima-media thickness and coronary artery calcium (CAC). We calculated event rates and the number needed to scan (NNS) to identify one participant with CAC>0 and > 100. Results: Over 10.4 years median follow-up, there were 33 events (2.4%) in participants with low lifetime risk. There were 479 participants (34%) with CAC>0 including 183 (13%) with CAC>100. CAC was present in 25 (76%) participants who experienced an event. In multivariable analyses, only CAC>100 remained predictive of CHD (HR 4.6; 95% CI: 1.6-13.6; p = 0.005). The event rates for CAC = 0, CAC>0 and CAC>100 were 0.9/1,000, 5.7/1,000, and 11.0/1000 person-years, respectively. The NNS to identify one participant with CAC>0 and > 100 were 3 and 7.6, respectively. Conclusions: While 10-year event rates were low in those with low lifetime risk, CAC was the strongest predictor of incident CHD. Identification of individuals with CAC = 0 and CAC>100 carries significant potential therapeutic implications.
AB - Aims: Patients with a low lifetime risk of coronary heart disease (CHD) are not completely free of events over 10 years. We evaluated predictors for CHD among "low lifetime risk" participants in the population-based Multi-Ethnic Study of Atherosclerosis (MESA). Methods: MESA enrolled 6814 men and women aged 45-84 years who were free of baseline cardiovascular disease. Using established criteria of non-diabetic, non-smokers with total cholesterol ≤200 mg/dL, systolic BP ≤ 139 mmHg, and diastolic BP ≤ 89 mmHg at baseline, we identified 1391 participants with a low lifetime risk for cardiovascular disease. Baseline covariates were age, gender, ethnicity, HDL-C, C-reactive protein, family history of CHD, carotid intima-media thickness and coronary artery calcium (CAC). We calculated event rates and the number needed to scan (NNS) to identify one participant with CAC>0 and > 100. Results: Over 10.4 years median follow-up, there were 33 events (2.4%) in participants with low lifetime risk. There were 479 participants (34%) with CAC>0 including 183 (13%) with CAC>100. CAC was present in 25 (76%) participants who experienced an event. In multivariable analyses, only CAC>100 remained predictive of CHD (HR 4.6; 95% CI: 1.6-13.6; p = 0.005). The event rates for CAC = 0, CAC>0 and CAC>100 were 0.9/1,000, 5.7/1,000, and 11.0/1000 person-years, respectively. The NNS to identify one participant with CAC>0 and > 100 were 3 and 7.6, respectively. Conclusions: While 10-year event rates were low in those with low lifetime risk, CAC was the strongest predictor of incident CHD. Identification of individuals with CAC = 0 and CAC>100 carries significant potential therapeutic implications.
KW - Coronary artery calcium
KW - Coronary heart disease
KW - Epidemiology
KW - Lifetime risk
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UR - http://www.scopus.com/inward/citedby.url?scp=84960885879&partnerID=8YFLogxK
U2 - 10.1016/j.atherosclerosis.2016.01.017
DO - 10.1016/j.atherosclerosis.2016.01.017
M3 - Article
C2 - 26841074
AN - SCOPUS:84960885879
SN - 0021-9150
VL - 246
SP - 367
EP - 373
JO - Atherosclerosis
JF - Atherosclerosis
ER -