[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.

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