Background Current strategies for
cardiovascular disease (CVD) risk assessment focus on 10-year or longer timeframes. Shorter-term CVD risk is also clinically relevant, particularly for high-risk occupations, but is under-investigated. Methods and Results We pooled data from participants in the ARIC (
Atherosclerosis Risk in Communities study), MESA (Multi-Ethnic Study of
Atherosclerosis), and DHS (Dallas Heart Study), free from CVD at baseline (N=16 581). Measurements included N-terminal pro-
B-type natriuretic peptide (>100 pg/mL prospectively defined as abnormal); high-sensitivity cardiac
troponin T (abnormal >5 ng/L);
high-sensitivity C-reactive protein (abnormal >3 mg/L);
left ventricular hypertrophy by ECG (abnormal if present); carotid intima-media thickness, and plaque (abnormal >75th percentile for age and sex or presence of plaque); and coronary artery
calcium (abnormal >10 Agatston U). Each abnormal test result except
left ventricular hypertrophy by ECG was independently associated with increased 3-year risk of global CVD (
myocardial infarction,
stroke, coronary revascularization, incident
heart failure, or
atrial fibrillation), even after adjustment for traditional CVD risk factors and the other test results. When a simple integer score counting the number of abnormal tests was used, 3-year multivariable-adjusted global CVD risk was increased among participants with integer scores of 1, 2, 3, and 4, by ≈2-, 3-, 4.5- and 8-fold, respectively, when compared with those with a score of 0. Qualitatively similar results were obtained for atherosclerotic CVD (fatal or non-fatal
myocardial infarction or
stroke). Conclusions A strategy incorporating multiple
biomarkers and
atherosclerosis imaging improved assessment of 3-year global and atherosclerotic CVD risk compared with a standard approach using traditional risk factors.