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ABSTRACT: Introduction
Clopidogrel is the most frequently utilized P2Y12 inhibitor and is characterized by broad interindividual response variability resulting in impaired platelet inhibition and increased risk of thrombotic complications in a considerable number of patients. The potent P2Y12 inhibitors, prasugrel and ticagrelor, can overcome this limitation but at the expense of an increased risk of bleeding. Genetic variations of the cytochrome P450 (CYP) 2 C19 enzyme, a key determinant in clopidogrel metabolism, have been strongly associated with clopidogrel response profiles prompting investigations of genetic-guided selection of antiplatelet therapy.Areas covered
The present manuscript focuses on the rationale for the use of genetic testing to guide the sel
SUBMITTER: Galli M
PROVIDER: S-EPMC9008593 | biostudies-literature | 2021 Aug
REPOSITORIES: biostudies-literature