Prospective CYP2C19 Genotyping to Guide Antiplatelet Therapy Following Percutaneous Coronary Intervention: A Pragmatic Randomized Clinical Trial

loss-of-function alleles impair clopidogrel effectiveness after percutaneous coronary intervention, but the clinical impact of implementing genotyping in a real-world setting is unknown. The purpose of the study was to determine whether returning genotype results along with genotype-guided pharmacot...

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Veröffentlicht in:Circulation. Genomic and precision medicine 2020-02, Vol.13 (1), p.e002640-e002640
Hauptverfasser: Tuteja, Sony, Glick, Henry, Matthai, William, Nachamkin, Irving, Nathan, Ashwin, Monono, Karen, Carcuffe, Craig, Maslowski, Karen, Chang, Gene, Kobayashi, Taisei, Anwaruddin, Saif, Hirshfeld, John, Wilensky, Robert L., Herrmann, Howard C., Kolansky, Daniel M., Rader, Daniel J., Giri, Jay
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Sprache:eng
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Zusammenfassung:loss-of-function alleles impair clopidogrel effectiveness after percutaneous coronary intervention, but the clinical impact of implementing genotyping in a real-world setting is unknown. The purpose of the study was to determine whether returning genotype results along with genotype-guided pharmacotherapy recommendations using a rapid turnaround test would change antiplatelet prescribing following percutaneous coronary intervention.The primary outcome was the rate of prasugrel or ticagrelor prescribing in each arm. Secondary outcomes included agreement to the genotype-guided recommendations. At the time of percutaneous coronary intervention, participants were randomly assigned to prospective rapid point-of-care genotyping of major alleles (*2, *3, *17) via salivary swab (genotyped group) or no genotyping (usual care) to guide antiplatelet drug selection. Interventional cardiologists at 2 cardiac catheterization laboratories within the same health system were provided genotype information along with genotype-guided pharmacotherapy recommendations. A total of 504 participants were randomized, 249 to the genotyped and 255 to the usual care group. The participants were primarily men (73%); age, 63±10 years; and 50% had acute coronary syndromes. In the genotyped group, 28% were carriers of loss-of-function alleles (*2, *3). The use of prasugrel or ticagrelor was significantly higher in the genotyped group compared with the usual care group (30% versus 21%; odds ratio, 1.60 [95% CI, 1.07-2.42]; =0.03). Within the genotyped group, 53% of loss-of-function allele carriers were started on prasugrel/ticagrelor, while 47% were started on clopidogrel. In a randomized controlled trial of clinical genotyping implementation, pharmacogenetic test results significantly influenced antiplatelet drug prescribing; however, almost half of loss-of-function carriers continued to receive clopidogrel. Interventional cardiologists consider both clinical and genetic factors when selecting antiplatelet therapy following percutaneous coronary intervention. URL: http://www.clinicaltrials.gov. Unique Identifier: NCT02508116.
ISSN:2574-8300
2574-8300
DOI:10.1161/CIRCGEN.119.002640