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Epoxidase inhibitor-aspirin resistance and the relationship with genetic polymorphisms: a review
1Department of Emergency Medicine, Zigong First People's Hospital, Zigong City, China.
Aspirin resistance, a cause of cardiovascular and cerebrovascular diseases, is linked to gene polymorphisms. Understanding these genetic variations can improve antiplatelet therapy guidance for at-risk patients.
Area of Science:
- Cardiovascular Science
- Pharmacogenomics
- Molecular Biology
Background:
- Strokes are a leading global cause of death, with aspirin (acetylsalicylic acid) widely used for prevention.
- Aspirin resistance, where patients still experience ischaemic events, hinders effective treatment and prevention strategies.
- Factors influencing aspirin resistance include genetics, drug dosage, and drug interactions.
Approach:
- This narrative review synthesizes current research on gene polymorphisms associated with aspirin resistance.
- The review focuses on how genetic variations in platelet receptors and aggregation pathways contribute to treatment failure.
- Analysis of existing literature to identify significant gene polymorphisms linked to aspirin resistance.
Key Points:
- Genetic polymorphism, the presence of multiple gene variants in a population, plays a crucial role in aspirin resistance.
- Polymorphisms in genes encoding platelet transmembrane glycoprotein receptors can alter platelet aggregation, leading to resistance.
- Specific gene polymorphisms have been identified as significantly associated with the development of aspirin resistance.
Conclusions:
- Understanding the mechanisms of aspirin resistance, particularly the role of gene polymorphisms, is essential for personalized medicine.
- Increased knowledge of pharmacogenomics can lead to more accurate drug guidance for individuals requiring antiplatelet therapy.
- Future research should focus on elucidating specific genetic markers to optimize aspirin treatment strategies.
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