Black or African American CYP2C19 clopidogrel genetic testing percutaneous coronary intervention precision medicine

Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
14 Jun 2024
Historique:
medline: 14 6 2024
pubmed: 14 6 2024
entrez: 14 6 2024
Statut: aheadofprint

Résumé

Cytochrome P450 2C19 (CYP2C19) intermediate and poor metabolizer patients exhibit diminished clopidogrel clinical effectiveness after percutaneous coronary intervention (PCI). However, outcome studies to date have lacked racial diversity. Thus, the impact of Adults among 5 institutions who self-identified as Black or African American, underwent PCI and clinical Black patients with CYP2C19 intermediate and poor metabolizer phenotypes who are treated with clopidogrel exhibit increased risk of adverse cardiovascular outcomes after PCI in a real-world clinical setting. Bleeding outcomes should be interpreted cautiously. Prospective studies are needed to determine whether genotype-guided use of prasugrel or ticagrelor in intermediate and poor metabolizers improves outcomes in Black patients undergoing PCI.

Sections du résumé

BACKGROUND BACKGROUND
Cytochrome P450 2C19 (CYP2C19) intermediate and poor metabolizer patients exhibit diminished clopidogrel clinical effectiveness after percutaneous coronary intervention (PCI). However, outcome studies to date have lacked racial diversity. Thus, the impact of
METHODS AND RESULTS RESULTS
Adults among 5 institutions who self-identified as Black or African American, underwent PCI and clinical
CONCLUSIONS CONCLUSIONS
Black patients with CYP2C19 intermediate and poor metabolizer phenotypes who are treated with clopidogrel exhibit increased risk of adverse cardiovascular outcomes after PCI in a real-world clinical setting. Bleeding outcomes should be interpreted cautiously. Prospective studies are needed to determine whether genotype-guided use of prasugrel or ticagrelor in intermediate and poor metabolizers improves outcomes in Black patients undergoing PCI.

Identifiants

pubmed: 38874073
doi: 10.1161/JAHA.123.033791
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e033791

Auteurs

Kayla R Tunehag (KR)

Division of Pharmacotherapy and Experimental Therapeutics, Eshelman School of Pharmacy University of North Carolina at Chapel Hill Chapel Hill NC USA.

Cameron D Thomas (CD)

Department of Pharmacotherapy & Translational Research and Center for Pharmacogenomics and Precision Medicine College of Pharmacy, University of Florida Gainesville FL USA.

Francesco Franchi (F)

Division of Cardiology, Department of Medicine College of Medicine-Jacksonville, University of Florida Jacksonville FL USA.

Joseph S Rossi (JS)

Division of Cardiology and McAllister Heart Institute, School of Medicine University of North Carolina at Chapel Hill Chapel Hill NC USA.

Ellen C Keeley (EC)

Division of Cardiovascular Medicine College of Medicine, University of Florida Gainesville FL USA.

R David Anderson (RD)

Division of Cardiovascular Medicine College of Medicine, University of Florida Gainesville FL USA.

Amber L Beitelshees (AL)

University of Maryland School of Medicine Department of Medicine and Program for Personalized and Genomic Medicine Baltimore MD USA.

Julio D Duarte (JD)

Department of Pharmacotherapy & Translational Research and Center for Pharmacogenomics and Precision Medicine College of Pharmacy, University of Florida Gainesville FL USA.

Yan Gong (Y)

Department of Pharmacotherapy & Translational Research and Center for Pharmacogenomics and Precision Medicine College of Pharmacy, University of Florida Gainesville FL USA.

Richard A Kerensky (RA)

Division of Cardiovascular Medicine College of Medicine, University of Florida Gainesville FL USA.

Caitrin W McDonough (CW)

Department of Pharmacotherapy & Translational Research and Center for Pharmacogenomics and Precision Medicine College of Pharmacy, University of Florida Gainesville FL USA.

Anh B Nguyen (AB)

Division of Pharmacotherapy and Experimental Therapeutics, Eshelman School of Pharmacy University of North Carolina at Chapel Hill Chapel Hill NC USA.

Luis Ortega-Paz (L)

Division of Cardiology, Department of Medicine College of Medicine-Jacksonville, University of Florida Jacksonville FL USA.

Sanjay Venkatesh (S)

Division of Cardiology, Duke Department of Medicine Duke University School of Medicine Durham NC USA.

Yehua Wang (Y)

Department of Pharmaceutical Outcomes & Policy, Department of Epidemiology, and Center for Drug Evaluation and Safety University of Florida Gainesville FL USA.

Julie A Johnson (JA)

Department of Pharmacotherapy & Translational Research and Center for Pharmacogenomics and Precision Medicine College of Pharmacy, University of Florida Gainesville FL USA.
Division of Cardiovascular Medicine College of Medicine, University of Florida Gainesville FL USA.

Almut G Winterstein (AG)

Department of Pharmaceutical Outcomes & Policy, Department of Epidemiology, and Center for Drug Evaluation and Safety University of Florida Gainesville FL USA.

George A Stouffer (GA)

Division of Cardiology and McAllister Heart Institute, School of Medicine University of North Carolina at Chapel Hill Chapel Hill NC USA.

Dominick J Angiolillo (DJ)

Division of Cardiology, Department of Medicine College of Medicine-Jacksonville, University of Florida Jacksonville FL USA.

Larisa H Cavallari (LH)

Department of Pharmacotherapy & Translational Research and Center for Pharmacogenomics and Precision Medicine College of Pharmacy, University of Florida Gainesville FL USA.

Craig R Lee (CR)

Division of Pharmacotherapy and Experimental Therapeutics, Eshelman School of Pharmacy University of North Carolina at Chapel Hill Chapel Hill NC USA.
Division of Cardiology and McAllister Heart Institute, School of Medicine University of North Carolina at Chapel Hill Chapel Hill NC USA.

Classifications MeSH