Why the study?
Does genetic testing for CYP2C19 genotype and limitation of proton pump inhibitor interactions optimize treatment in patients taking clopidogrel?
Does genetic testing for CYP2C19 genotype and limitation of proton pump inhibitor interactions optimize treatment in patients taking clopidogrel?
Routine genetic testing for CYP2C19 and avoidance of PPIs in patients taking clopidogrel are not currently recommended based on available evidence.
Answers are grounded in this paper and cite their sources.
Does not support routine CYP2C19 testing or PPI avoidance with clopidogrel; leaves open whether targeted strategies merit prospective evaluation.
Clopidogrel is one of the most commonly prescribed medications worldwide. Recent advisories from the US Food and Drug Administration have drawn attention to the possibility of personalized decision-making for people who are candidates for clopidogrel. As is the case with antihypertensives, statins, and warfarin, common genetic sequence variants can influence clopidogrel metabolism and its effect on platelet activity. These genetic variants have, in multiple studies, been associated with adverse clinical outcomes. Concurrent medication use also influences how the body handles clopidogrel. Proton pump inhibitors, widely prescribed in conjunction with clopidogrel, may blunt its effectiveness. We address implications for bedside decision-making in light of accumulated data and current Food and Drug Administration advisories and conclude that genetic testing for CYP2C19 genotype and limitation of proton pump inhibitor interactions do not yet appear to offer an opportunity to optimize treatment given the current state of knowledge.
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Anderson et al. (2010) studied this question.
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