Key result
Lipophilic statins metabolized through CYP3A4 do not influence the antiplatelet effectiveness of clopidogrel in patients undergoing elective percutaneous coronary intervention.
Why the study?
Do lipophilic statins metabolized through CYP3A4 reduce the antiplatelet effectiveness of clopidogrel in patients undergoing elective percutaneous coronary intervention?
Do lipophilic statins metabolized through CYP3A4 reduce the antiplatelet effectiveness of clopidogrel in patients undergoing elective percutaneous coronary intervention?
Co-administration of CYP3A4-metabolized lipophilic statins does not attenuate the antiplatelet efficacy of clopidogrel during maintenance therapy.
This letter to the editor discusses the results of the recently published study by Smith et al. which demonstrated that lipophilic statins metabolized through the cytochrome P--450 isoform 3A4 (CYP3A4) do not influence the antiplatelet effectiveness of clopidogrel in patients undergoing elective percutaneous coronary intervention. These results as well as those of other recent studies suggest that there is no adverse interaction between clopidogrel and CYP3A4-metabolized statins, during the maintenance phase of therapy (i.e., 2 or more days after the drug co-administration) either at the platelet or at the clinical level.
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Tselepis et al. (2005) conducted a letter in Elective percutaneous coronary intervention. Lipophilic statins metabolized through CYP3A4 was evaluated on Antiplatelet effectiveness of clopidogrel. Lipophilic statins metabolized through CYP3A4 do not influence the antiplatelet effectiveness of clopidogrel in patients undergoing elective percutaneous coronary intervention.
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