Why the study?
Individual variability in clopidogrel antiplatelet effects and the clinical significance of the smokers paradox remain important clinical concerns in patients with coronary artery disease.
This review highlights the 'smoker's paradox', suggesting that smoking may enhance the antiplatelet efficacy of clopidogrel in patients with coronary artery disease.
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Variability in clopidogrel response and smoker’s paradox remain clinically relevant; leaves open need for personalized strategies in post-MI patients.
Clopidogrel is the most widely used P2Y12 inhibitor, which is administered for secondary prevention of atherothrombotic events in patients with cardiovascular disease after myocardial infarction and coronary stenting. Given the complexity of the clopidogrel metabolism and variety of potential drug-drug interactions, the issue of individual variability of its antiplatelet effects is of paramount concern. Another issue of clinical relevance is related to so-called “smoker’s paradox”. This phenomenon implies that in some patients smoking is associated with increased antiplatelet potency of clopidogrel. In this review, we analyze recent international data on the features of pharmacokinetics and pharmacodynamics of clopidogrel, plausible mechanisms of the “smoker’s paradox” and its clinical significance in patients with coronary artery disease. Comparative efficacy of available P2Y12 inhibitors and possible implications of smoking are considered. Pharmacogenetic aspects and the issues of personalized antiplatelet therapy are discussed.
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Lukianets et al. (2020) studied this question.
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