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Updated: Jan 20, 2026

Identifying Coronary Artery Calcification on Non-gated Computed Tomography Scans
Published on: August 28, 2018
Usefulness of Coronary Artery Calcium to Identify Adults of Sufficiently High Risk for Atherothrombotic
Kelly Arps1, Mahmoud Al Rifai1, Michael J Blaha1
1Johns Hopkins Ciccarone Center for the Prevention of Cardiovascular Disease, Baltimore, Maryland.
Insights
Coronary artery calcium (CAC) scoring identifies high-risk individuals for atherosclerotic cardiovascular disease (ASCVD) primary prevention. Low-dose rivaroxaban may offer net benefit for those with CAC 100-299 or ≥300, balancing ASCVD event reduction against bleeding risk.
Area of Science:
- Cardiology
- Preventive Medicine
- Pharmacology
Background:
- Low-dose rivaroxaban demonstrated efficacy in secondary prevention of atherosclerotic cardiovascular disease (ASCVD) within the COMPASS trial.
- The role of oral anticoagulants in primary prevention of ASCVD remains undefined.
- Coronary artery calcium (CAC) scoring is a tool for assessing subclinical atherosclerosis.
Purpose of the Study:
- To evaluate if CAC scoring can identify high-risk primary prevention adults who may benefit from low-dose rivaroxaban for ASCVD event prevention.
- To model the number needed to treat (NNT) and number needed to harm (NNH) for low-dose rivaroxaban in primary prevention stratified by CAC scores.
Main Methods:
- Utilized data from 5,196 Multiethnic Study of Atherosclerosis (MESA) cohort participants not on antiplatelet or anticoagulant therapy.
- Applied relative risk ratios from the COMPASS trial to MESA cohort absolute event rates.
- Stratified NNT and NNH by calculated ASCVD risk and baseline CAC scores to estimate net clinical benefit.
Main Results:
- Participants with CAC ≥300 exhibited an ASCVD event rate of 20 per 1000 patient-years, comparable to the COMPASS control arm.
- CAC score was independently associated with ASCVD outcomes (p <0.001 for trend) but not independently with major bleeding risk.
- Predicted 5-year NNT was 75 for CAC 100-299 and 45 for CAC ≥300, with corresponding NNH values of 252 and 98.
Conclusions:
- CAC scoring aids in distinguishing potential ASCVD event reduction benefits from bleeding risks associated with low-dose rivaroxaban.
- Identifies very high-risk primary prevention adults without established cardiovascular disease who may achieve net benefit from low-dose rivaroxaban therapy.
Abstract:
Low-dose rivaroxaban was effective in secondary prevention of atherosclerotic cardiovascular disease (ASCVD) in the COMPASS trial. There is no established role, however, for oral anticoagulants in primary prevention. We evaluated whether coronary artery calcium (CAC) scoring identifies a high-risk primary prevention adult population who may benefit from low-dose rivaroxaban to prevent ASCVD events. We modeled expected outcomes of low-dose rivaroxaban in 5,196 Multiethnic Study of Atherosclerosis (MESA) cohort participants not already on antiplatelet or anticoagulant therapy. We applied relative risk ratios from COMPASS to absolute MESA event rates in order to estimate number needed to treat (NNT) to avoid a composite of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke, as well as number needed to harm (NNH) to cause 1 hospitalized bleed; with both NNT and NNH stratified by calculated ASCVD risk and by baseline CAC. MESA participants with CAC ≥300 had crude ASCVD event rate of 20 per 1000 patient-years, which is comparable to that observed in the COMPASS control-arm. CAC was independently associated with the composite ASCVD outcome (p <0.001 for trend). However, CAC was not independently associated with adjusted hazard ratio for hospitalized major bleeding. Predicted 5-year NNT (modeled from COMPASS) was 75 in persons with CAC 100-299 and 45 with CAC ≥300 despite NNH values of 252 and 98, respectively. In conclusion, CAC helps to distinguish estimated ASCVD benefit from estimated bleeding harm, thereby identifying very high-risk primary prevention adults without established cardiovascular disease who may derive net-benefit from low-dose rivaroxaban.
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