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Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
[Algorithm for selection of individual therapy with clopidogrel in vascular surgical practice]
A I Shevela1, A A Slepukhina1, E M Zelenskaya1
1Institute of Chemical Biology and Fundamental Medicine of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.
Insights
Antiplatelet therapy with clopidogrel is crucial for lower limb artery diseases. Individualized dosing based on platelet aggregation and CYP2C19 gene testing optimizes treatment efficacy and safety.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Genetics
Background:
- Permanent antiplatelet therapy is indicated for lower limb artery diseases and high-risk cardiovascular patients.
- Individual sensitivity to antiplatelet agents like clopidogrel poses a clinical challenge.
- Clopidogrel, a thienopyridine prodrug, requires two-stage metabolism via cytochrome P450 2C19 (CYP2C19) to exert its antiplatelet effect.
Purpose of the Study:
- To develop an individualized dosing algorithm for clopidogrel in patients with atherosclerosis of lower limb arteries.
- To enhance the efficacy and safety of antiplatelet therapy by considering individual patient factors.
- To correlate platelet aggregation levels and CYP2C19 genetic variations with clopidogrel response.
Main Methods:
- Analysis of patient case histories with atherosclerosis of lower limb arteries.
- Assessment of platelet aggregation levels in response to various inducers (ADP, collagen, arachidonic acid).
- Molecular-genetic testing for cytochrome CYP2C19 gene variations.
Main Results:
- An evidence-supported basis for long-term clopidogrel use in lower limb artery atherosclerosis was established.
- A novel algorithm for individualized clopidogrel dosing was developed, incorporating platelet aggregation data.
- Dose correction based on CYP2C19 genetic testing results was integrated into the algorithm.
- The algorithm aims to maximize treatment efficacy and patient safety.
Conclusions:
- Individualized clopidogrel dosing, guided by platelet aggregation and CYP2C19 genotype, is essential for optimizing antiplatelet therapy.
- This approach addresses variable patient sensitivity and improves therapeutic outcomes in lower limb artery disease.
- The developed algorithm offers a personalized strategy for clopidogrel management.
Abstract:
For treatment of patients with diseases of lower limb arteries and prevention of cardiovascular complications in high-risk patients (those with diabetes mellitus, arterial hypertension, dyslipidemia, obesity) permanent antiplatelet therapy is indicated. A problem is variable individual sensitivity to therapeutic agents. For antiplatelet therapy in patients with atherosclerosis of lower limb arteries there has been obtained an evidence-supported base concerning efficacy of long-term administration of clopidogrel preparations, unlike patients with acute coronary syndrome, for whom there has been accumulated an evidence-confirmed base of administering clopidogrel preparations, as well as ticagrelor and prasugrel in various clinical situations. Clopidogrel is currently the best known representative from the group of thienopyridines. It is a pro-drug and has complicated metabolism: two-stage oxidation under the effect of isoforms of cytochrome 2C19. Its active form irreversibly inhibits binding of ADP with P2Y12 receptors of thrombocytes. This is followed by inhibition of binding of fibrinogen with the glycoprotein IIb/IIIa receptor and a decrease of aggregation. Determining blood platelet aggregation with ADP, collagen and arachidonic acid forms the basis of clinical assessment of the functional state of thrombocytic activity and may be a marker of efficacy of treatment with antiaggregants. A complicated mechanism of action of clopidogrel implies individual policy of the attending physician in making a decision concerning the duration of therapy and selection of the dose. These prerequisites resulted in working out a recommended algorithm of individual dosing of clopidogrel (based on the analysis of case histories of patients with atherosclerosis of lower limb arteries by the level of platelet aggregation to a series of inducers) and correction of the dose of the drug based on the results of molecular-genetic testing of the cytochrome CYPC19 gene. The algorithm makes it possible to achieve a maximum level of efficacy and safety of treatment with antiaggregants.
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