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. 2011 Jun 26;32(4):459–466. doi: 10.1007/s11239-011-0611-8

Table 2.

Expected effects of CYP2C19 polymorphism on clopidogrel metabolism

Genotype Expected effect on clopidogrel metabolism
CYP2C19*1/*1 Normal metabolizer—the subject is expected to demonstrate effective antiplatelet response to a standard dose of clopidogrel
CYP2C19*1/*2 Intermediate metabolizer—the subject exhibits approximately half-normal enzyme activity, thus an increased dosage of clopidogrel or an alternative treatment should be considered
CYP2C19*1/*3
CYP2C19*1/*4
CYP2C19*1/*5
CYP2C19*2/*17 Normal/intermediate metabolizer—the subject is likely to have metabolic activity between normal and intermediate metabolizers. In general, the response to a standard dose of clopidogrel should be sufficient
CYP2C19*3/*17
CYP2C19*4/*17
CYP2C19*5/*17
CYP2C19*2/*2 Poor metabolizer—the subject is characterized by a greatly decreased enzyme activity and may require an alternative treatment or higher than standard dosage of clopidogrel to achieve required antiplatelet effect
CYP2C19*2/*3
CYP2C19*2/*4
CYP2C19*2/*5
Or other configuration of these alleles
CYP2C19*1/*17 Rapid metabolizer—the subject have elevated enzyme activity and may be exposed to a higher concentration of active drug metabolites resulting in increased bleeding risk
CYP2C19*17/*17 Ultra rapid metabolizer—the subject have markedly elevated enzyme activity. For prodrugs, like clopidogrel, ultra rapid metabolizers are exposed to a higher concentration of active drug metabolites and may require lower than standard dosage because of increased risk of bleeding