Why the study?
To provide an overview of the background and rationale for using a guided antiplatelet approach to enhance patient care.
Does CYP2C19 genetic testing improve outcomes in patients with acute coronary syndromes, stroke, or undergoing percutaneous coronary intervention?
Does CYP2C19 genetic testing improve outcomes in patients with acute coronary syndromes, stroke, or undergoing percutaneous coronary intervention?
CYP2C19 genetic testing provides a viable strategy to individualize antiplatelet therapy and guide the selection of P2Y12 inhibitors in clinical practice.
May support CYP2C19-guided P2Y12 selection in ACS/PCI; leaves open need for outcome trials.
Antiplatelet therapy is used in the treatment of patients with acute coronary syndromes, stroke, and those undergoing percutaneous coronary intervention. Clopidogrel is the most widely used antiplatelet P2Y12 inhibitor in clinical practice. Genetic variation in CYP2C19 may influence its enzymatic activity, resulting in individuals who are carriers of loss-of-function CYP2C19 alleles and thus have reduced active clopidogrel metabolites, high on-treatment platelet reactivity, and increased ischemic risk. Prospective studies have examined the utility of CYP2C19 genetic testing to guide antiplatelet therapy, and more recently published meta-analyses suggest that pharmacogenetics represents a key treatment strategy to individualize antiplatelet therapy. Rapid genetic tests, including bedside genotyping platforms that are validated and have high reproducibility, are available to guide selection of P2Y12 inhibitors in clinical practice. The aim of this review is to provide an overview of the background and rationale for the role of a guided antiplatelet approach to enhance patient care.
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Castrichini et al. (2022) studied this question.
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