In adults (men < 60 y, women < 70 y) with low‑to‑moderate bleeding risk and a 10‑year atherosclerotic cardiovascular disease risk ≈5%, at what coronary artery calcium score should low‑dose aspirin be started for primary prevention?

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Last updated: February 27, 2026View editorial policy

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Recommended Coronary Artery Calcium Threshold for Starting Aspirin in Primary Prevention

For adults with low-to-moderate bleeding risk and approximately 5% 10-year ASCVD risk, aspirin should be started when the coronary artery calcium (CAC) score is ≥100. 1

CAC-Based Decision Algorithm

CAC ≥100: Consider Aspirin

  • Low-dose aspirin (75-100 mg daily, typically 81 mg in the U.S.) is reasonable for patients with CAC ≥100 who have low bleeding risk. 1
  • Multiple international guidelines—including the American College of Cardiology/American Heart Association (ACC/AHA), Society of Cardiovascular Computed Tomography (SCCT), National Lipid Association (NLA), Cardiac Society of Australia and New Zealand (CSANZ), and Chinese guidelines—explicitly endorse CAC ≥100 as the threshold where aspirin's cardiovascular benefit exceeds bleeding risk. 1
  • At CAC ≥100, the estimated 5-year number-needed-to-treat is 173 for individuals with <10% Framingham Risk Score and 92 for those ≥10%, compared to a number-needed-to-harm of 442 for major bleeding. 2
  • Patients with CAC >400 derive even greater net benefit, with aspirin yielding favorable outcomes regardless of traditional risk factors. 1

CAC = 0: Do Not Start Aspirin

  • Aspirin is not recommended when CAC = 0, even if calculated ASCVD risk is moderate (≈5%), because the bleeding risk outweighs any cardiovascular benefit. 1, 3
  • A CAC score of zero reflects minimal atherosclerotic burden and very low near-term event risk; the estimated 5-year number-needed-to-treat is 2,036 for individuals <10% FRS and 808 for those ≥10% FRS, making the risk-benefit ratio unfavorable. 2
  • The only exception is patients with CAC = 0 who have >20% 10-year ASCVD risk, though this scenario is rare in the population described in your question. 1

CAC 1-99: Generally Do Not Start Aspirin

  • Evidence is mixed for this intermediate range; aspirin is generally not recommended unless multiple additional high-risk features are present (e.g., strong family history of premature ASCVD, markedly elevated lipoprotein(a), chronic kidney disease with albuminuria). 3

Why CAC Outperforms Traditional Risk Scores

  • The pooled cohort equations (PCE) systematically overestimate actual ASCVD risk in contemporary populations receiving optimal statin and blood pressure therapy. 3, 4
  • CAC directly visualizes coronary plaque burden, providing more accurate risk stratification than PCE-derived estimates, especially when traditional risk factors are well-controlled. 3
  • In patients with ≈5% 10-year ASCVD risk, the number of cardiovascular events prevented by aspirin roughly equals the number of major bleeding episodes induced when using traditional risk scores alone, resulting in near-neutral net benefit. 4
  • CAC scoring identifies the subset of intermediate-risk patients who harbor sufficient subclinical atherosclerosis to tip the balance toward net benefit. 5

Absolute Contraindications to Aspirin (Even with CAC ≥100)

Do not prescribe aspirin if any of the following are present:

  • Age >70 years (bleeding risk exceeds cardiovascular benefit regardless of CAC score) 3, 6
  • History of gastrointestinal bleeding or active peptic ulcer disease 3, 7
  • Known bleeding disorder or thrombocytopenia 3, 7
  • Concurrent use of oral anticoagulants (warfarin or DOACs), NSAIDs, or systemic corticosteroids 3, 7
  • Severe liver disease 3
  • Chronic kidney disease (increases bleeding risk substantially) 3, 7
  • Uncontrolled hypertension 3

Practical Implementation for Your Patient Population

For adults (men <60 years, women <70 years) with ≈5% 10-year ASCVD risk and low-to-moderate bleeding risk:

  1. Obtain CAC scoring to refine risk stratification beyond traditional calculators. 1, 5
  2. If CAC ≥100: Initiate aspirin 75-100 mg daily (81 mg standard U.S. tablet) after shared decision-making that emphasizes the modest benefit (≈1 cardiovascular event prevented per 100 patients treated over 5-10 years) balanced against ≈1 major bleeding event. 3, 4
  3. If CAC <100: Do not start aspirin; focus on optimizing statin therapy, blood pressure control, smoking cessation, and lifestyle modification, which have stronger evidence for ASCVD risk reduction. 3, 4
  4. Reassess bleeding risk regularly; discontinue aspirin if the patient develops new bleeding risk factors or ages beyond 70 years. 4

Common Pitfalls to Avoid

  • Do not use the 10% 10-year ASCVD risk threshold alone to initiate aspirin; without CAC stratification, the benefit-to-harm balance is unfavorable in contemporary practice. 3, 8
  • Do not exceed 100 mg daily aspirin dose for primary prevention; higher doses increase bleeding risk without additional cardiovascular benefit. 3, 7
  • Do not overlook bleeding risk factors when calculating net benefit; real-world major bleeding rates are approximately 5 per 1,000 patients per year. 3, 4
  • Do not assume aspirin reduces cardiovascular mortality; the primary benefit is a 12% reduction in non-fatal myocardial infarction, with minimal effect on cardiovascular death (relative risk ≈0.95). 4

Strength of Evidence

The CAC ≥100 threshold is supported by:

  • Multiple high-quality observational cohort studies (Multi-Ethnic Study of Atherosclerosis and others) demonstrating graded increases in cardiovascular events corresponding to CAC scores. 2
  • Formal endorsement by major international guideline bodies (ACC/AHA, SCCT, NLA, CSANZ, Chinese guidelines) published in 2023, representing the most recent consensus. 1
  • Meta-analyses showing that CAC ≥100 identifies patients in whom aspirin's cardiovascular benefit exceeds bleeding risk, whereas CAC = 0 identifies those who would experience net harm. 1, 8

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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