Higher on-clopidogrel platelet reactivity was observed as the number of CYP2C19 LOF allele increased (UM 4.0; EM, 177.7; IM, 201.7; and PM 277.0), but post hoc analysis did not reach statistical significance for linear trend, probably as a result of the small number of patients.
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Feasibility of a microarray-based point-of-care CYP2C19 genotyping test for predicting clopidogrel on-treatment platelet reactivity.
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