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Low-dose aspirin increases aspirin resistance in patients with coronary artery disease
Pui-Yin Lee1, Wai-Hong Chen, William Ng
1Department of Medicine, The University of Hong Kong, Queen Mary Hospital, China.
Insights
Lower daily aspirin doses (≤100 mg) are linked to increased aspirin resistance in coronary artery disease patients. Higher doses may offer better platelet inhibition for preventing cardiovascular events.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Aspirin is a cornerstone therapy for preventing atherothrombotic events.
- Aspirin resistance, defined as inadequate platelet inhibition, is a growing concern.
- Understanding factors influencing aspirin resistance is crucial for optimizing patient outcomes.
Purpose of the Study:
- To investigate the association between aspirin dosage and aspirin resistance.
- To identify predictors of aspirin resistance in stable coronary artery disease (CAD) patients.
Main Methods:
- A study of 468 stable CAD patients taking daily aspirin (80-325 mg) for at least 4 weeks.
- Aspirin responsiveness was measured using the VerifyNow Aspirin point-of-care assay.
- Demographic and clinical data were collected to analyze predictors of resistance.
Main Results:
- Aspirin resistance was observed in 27.4% of patients.
- Lower aspirin doses (≤100 mg daily) were independently associated with higher aspirin resistance.
- Hemoglobin levels and aspirin dose were identified as independent predictors of resistance.
Conclusions:
- Daily aspirin doses of 100 mg or less are associated with a higher incidence of aspirin resistance in CAD patients.
- Lower doses, while potentially having fewer side effects, may compromise therapeutic efficacy.
- Further randomized trials are needed to determine optimal aspirin dosing for preventing ischemic complications.
Purpose:
We sought to investigate the association of aspirin dose and aspirin resistance in stable coronary artery disease patients measured by a point-of-care assay.
Methods:
We studied 468 consecutive stable coronary artery disease patients in a referral cardiac center who were taking aspirin 80 to 325 mg daily for > or =4 weeks. The VerifyNow Aspirin (Ultegra RPFA-ASA, Accumetrics Inc, San Diego, Calif) was used to determine aspirin responsiveness. An aspirin reaction unit (ARU) > or =550 indicates the absence of aspirin-induced platelet dysfunction, based on correlation with epinephrine-induced light transmission aggregometry. Demographic and clinical data were collected to analyze the predictors of aspirin resistance.
Results:
Aspirin resistance was noted in 128 (27.4%) patients. Univariate predictors of aspirin resistance include elderly (P = 0.002), women (P <0.001), anemia (P <0.001), renal insufficiency (P = 0.009) and aspirin dose < or =100 mg (P = 0.004). Multivariate analysis revealed hemoglobin (odds ratio [OR] 0.6; 95% confidence interval [CI] 0.51 to 0.69; P <0.001) and aspirin dose < or =100 mg (OR 2.23; 95% CI 1.12 to 4.44; P = 0.022) to be independent predictors of aspirin resistance. Daily aspirin dose < or = 100 mg was associated with increased prevalence of aspirin resistance compared with 150 mg and 300 mg daily (30.2% vs 16.7% vs 0%, P = 0.0062).
Conclusion:
A 100 mg or less daily dose of aspirin, which may have lower side effects, is associated with a higher incidence of aspirin resistance in patients with coronary artery disease. Prospective randomized studies are warranted to elucidate the optimal aspirin dosage for preventing ischemic complications of atherothrombotic disease.
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