Pharmacodynamic Effects of Atorvastatin vs. Rosuvastatin on Platelet Reactivity
Status:
Unknown status
Trial end date:
2015-06-01
Target enrollment:
Participant gender:
Summary
Patients with coronary artery disease (CAD) are often treated with dual antiplatelet therapy
(DAT), including aspirin and clopidogrel, to prevent from recurrent atherothrombotic events.
Levels of platelet reactivity in patients on DAT can be influenced by concomitant treatment
with medications that inhibit the CYP3A4 system involved in the activation of clopidogrel.
Atorvastatin and simvastatin are metabolized by CYP3A4 [Clin pharmacokinetic 2002; 41:
343-70], whereas the cytochrome P450 mediated metabolism of rosuvastatin appears to be
minimal and principally mediated by the 2C9 isoenzyme, with little involvement of CYP3A4
[Clin Ther 2003; 25: 2822-5.].
Previous studies comparing atorvastatin versus rosuvastatin by means of ex vivo platelet
function tests have yielded conflicting results.