Cyclooxygenase-1 haplotype modulates platelet response to aspirin
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Updated: Aug 3, 2026

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
A O Maree1, R J Curtin, A Chubb
1Department of Clinical Pharmacology, Royal College of Surgeons, Ireland. amaree@partners.org
Insights
Genetic variations in the cyclooxygenase-1 (COX-1) gene influence how individuals respond to aspirin therapy. This COX-1 gene variability may explain differences in aspirin effectiveness, particularly in cardiovascular disease patients.
Area of Science:
- Pharmacogenomics
- Cardiovascular Medicine
- Molecular Biology
Background:
- Aspirin (acetylsalicylic acid) inhibits platelet cyclooxygenase-1 (COX-1), crucial for thromboxane A2 production.
- Despite aspirin's benefits in cardiovascular disease (CAD), individual response variability, termed 'aspirin resistance,' is observed.
Purpose of the Study:
- To investigate if variations in the COX-1 gene influence aspirin response.
- To determine if COX-1 gene polymorphisms contribute to aspirin resistance in patients with stable CAD.
Main Methods:
- Studied 144 patients with stable CAD on aspirin (75-300 mg).
- Assessed aspirin response via serum thromboxane B2 (TXB2) levels and arachidonic acid (AA)-induced platelet aggregation.
- Genotyped patients for five single nucleotide polymorphisms (SNPs) in the COX-1 gene.
Main Results:
- COX-1 haplotype significantly correlated with AA-induced platelet aggregation (P = 0.004).
- Serum TXB2 generation was also associated with COX-1 genotype (P = 0.02).
Conclusions:
- Genetic variability in the COX-1 gene modulates platelet aggregation and thromboxane generation.
- Differences in patient response to aspirin may be partly explained by variations in COX-1 genotype.
Background:
Aspirin (acetylsalicylic acid) irreversibly inhibits platelet cyclooxygenase (COX)-1, the enzyme that converts arachidonic acid (AA) to the potent platelet agonist thromboxane (TX) A2. Despite clear benefit from aspirin in patients with cardiovascular disease (CAD), evidence of heterogeneity in the way individuals respond has given rise to the concept of 'aspirin resistance.'
Aims:
To evaluate the hypothesis that incomplete suppression of platelet COX as a consequence of variation in the COX-1 gene may affect aspirin response and thus contribute to aspirin resistance.
Patients And Methods:
Aspirin response, determined by serum TXB2 levels and AA-induced platelet aggregation, was prospectively studied in patients (n = 144) with stable CAD taking aspirin (75-300 mg). Patients were genotyped for five single nucleotide polymorphisms in COX-1 [A-842G, C22T (R8W), G128A (Q41Q), C644A (G213G) and C714A (L237M)]. Haplotype frequencies and effect of haplotype on two platelet phenotypes were estimated by maximum likelihood. The four most common haplotypes were considered separately and less common haplotypes pooled.
Results:
COX-1 haplotype was significantly associated with aspirin response determined by AA-induced platelet aggregation (P = 0.004; 4 d.f.). Serum TXB2 generation was also related to genotype (P = 0.02; 4 d.f.).
Conclusion:
Genetic variability in COX-1 appears to modulate both AA-induced platelet aggregation and thromboxane generation. Heterogeneity in the way patients respond to aspirin may in part reflect variation in COX-1 genotype.
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