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Multisite Investigation of Outcomes With Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention.

Authors :
Cavallari LH
Lee CR
Beitelshees AL
Cooper-DeHoff RM
Duarte JD
Voora D
Kimmel SE
McDonough CW
Gong Y
Dave CV
Pratt VM
Alestock TD
Anderson RD
Alsip J
Ardati AK
Brott BC
Brown L
Chumnumwat S
Clare-Salzler MJ
Coons JC
Denny JC
Dillon C
Elsey AR
Hamadeh IS
Harada S
Hillegass WB
Hines L
Horenstein RB
Howell LA
Jeng LJB
Kelemen MD
Lee YM
Magvanjav O
Montasser M
Nelson DR
Nutescu EA
Nwaba DC
Pakyz RE
Palmer K
Peterson JF
Pollin TI
Quinn AH
Robinson SW
Schub J
Skaar TC
Smith DM
Sriramoju VB
Starostik P
Stys TP
Stevenson JM
Varunok N
Vesely MR
Wake DT
Weck KE
Weitzel KW
Wilke RA
Willig J
Zhao RY
Kreutz RP
Stouffer GA
Empey PE
Limdi NA
Shuldiner AR
Winterstein AG
Johnson JA
Source :
JACC. Cardiovascular interventions [JACC Cardiovasc Interv] 2018 Jan 22; Vol. 11 (2), pp. 181-191. Date of Electronic Publication: 2017 Nov 01.
Publication Year :
2018

Abstract

Objectives: This multicenter pragmatic investigation assessed outcomes following clinical implementation of CYP2C19 genotype-guided antiplatelet therapy after percutaneous coronary intervention (PCI).<br />Background: CYP2C19 loss-of-function alleles impair clopidogrel effectiveness after PCI.<br />Methods: After clinical genotyping, each institution recommended alternative antiplatelet therapy (prasugrel, ticagrelor) in PCI patients with a loss-of-function allele. Major adverse cardiovascular events (defined as myocardial infarction, stroke, or death) within 12 months of PCI were compared between patients with a loss-of-function allele prescribed clopidogrel versus alternative therapy. Risk was also compared between patients without a loss-of-function allele and loss-of-function allele carriers prescribed alternative therapy. Cox regression was performed, adjusting for group differences with inverse probability of treatment weights.<br />Results: Among 1,815 patients, 572 (31.5%) had a loss-of-function allele. The risk for major adverse cardiovascular events was significantly higher in patients with a loss-of-function allele prescribed clopidogrel versus alternative therapy (23.4 vs. 8.7 per 100 patient-years; adjusted hazard ratio: 2.26; 95% confidence interval: 1.18 to 4.32; p = 0.013). Similar results were observed among 1,210 patients with acute coronary syndromes at the time of PCI (adjusted hazard ratio: 2.87; 95% confidence interval: 1.35 to 6.09; p = 0.013). There was no difference in major adverse cardiovascular events between patients without a loss-of-function allele and loss-of-function allele carriers prescribed alternative therapy (adjusted hazard ratio: 1.14; 95% confidence interval: 0.69 to 1.88; p = 0.60).<br />Conclusions: These data from real-world observations demonstrate a higher risk for cardiovascular events in patients with a CYP2C19 loss-of-function allele if clopidogrel versus alternative therapy is prescribed. A future randomized study of genotype-guided antiplatelet therapy may be of value.<br /> (Copyright © 2018 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1876-7605
Volume :
11
Issue :
2
Database :
MEDLINE
Journal :
JACC. Cardiovascular interventions
Publication Type :
Academic Journal
Accession number :
29102571
Full Text :
https://doi.org/10.1016/j.jcin.2017.07.022