Coronary Artery Calcium to Improve the Efficiency of Randomized Controlled Trials in Primary Cardiovascular

Miguel Cainzos-Achirica1, Marcio Sommer Bittencourt2, Albert D Osei3

  • 1Division of Cardiovascular Prevention and Wellness, Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas, USA; Center for Outcomes Research, Houston Methodist, Houston, Texas, USA; Johns Hopkins Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Insights

Coronary artery calcium (CAC) scoring effectively identifies high-risk individuals for atherosclerotic cardiovascular disease (ASCVD) primary prevention trials. Using CAC >400 significantly reduces sample size and costs for randomized controlled trials (RCTs).

Area of Science:

  • Cardiology
  • Preventive Medicine
  • Clinical Trial Design

Background:

  • Randomized controlled trials (RCTs) for primary prevention of atherosclerotic cardiovascular disease (ASCVD) face challenges in sample size and cost, particularly for novel add-on therapies.
  • High-risk individuals treated with statins are a key population for these trials.

Purpose of the Study:

  • To evaluate the utility of coronary artery calcium (CAC) scoring in enriching primary prevention RCT populations with individuals at high absolute risk of ASCVD events.
  • To assess the impact of CAC scoring on sample size and cost-efficiency in clinical trials.

Main Methods:

  • 3,075 statin-naive participants from the Multi-Ethnic Study of Atherosclerosis (MESA) with an estimated 10-year ASCVD risk of ≥7.5% were analyzed.
  • Coronary artery calcium (CAC) scores (>100, >400) and other biomarkers were assessed as enrichment criteria.
  • Projected 5-year cardiovascular disease (CVD) incidence, sample sizes, and costs for hypothetical RCTs were computed based on assumed relative risk reductions.

Main Results:

  • A CAC score >400 identified subgroups with the highest 5-year incident events, reducing projected sample size by 33%–58% compared to risk estimation alone.
  • Using CAC >400 resulted in the lowest projected RCT costs, with savings of at least $40 million.
  • A CAC score >100 demonstrated the second-best performance in most scenarios.

Conclusions:

  • High CAC scores serve as effective entry criteria for primary prevention RCTs.
  • Implementing CAC scoring enhances the efficiency and feasibility of trials evaluating novel add-on therapies for ASCVD prevention.
Abstract

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