The impact of CYP2C19 and CYP4F2 variants and clinical factors on treatment outcomes during antiplatelet therapy

被引:13
作者
Tatarunas, Vacis [1 ]
Kupstyte-Kristapone, Nora [1 ,2 ,3 ]
Norvilaite, Rita [4 ]
Tamakauskas, Vytenis [1 ,3 ]
Skipskis, Vilius [1 ]
Audrone, Veikutiene [1 ,5 ]
Jurgaityte, Julija [4 ]
Stuoka, Mantvydas [4 ]
Lesauskaite, Vaiva [1 ]
机构
[1] Lithuanian Univ Hlth Sci, Inst Cardiol, Sukileliu 17, LT-50009 Kaunas, Lithuania
[2] Lithuanian Univ Hlth Sci, Dept Cardiol, Eiveniu 2, LT-50009 Kaunas, Lithuania
[3] Republican Siauliai Hosp, Heart & Vasc Ctr, V Kudirkos G 99, LT-76231 Shiauliai, Lithuania
[4] Lithuanian Univ Hlth Sci, A Mickeviciaus 9, LT-44307 Kaunas, Lithuania
[5] Dept Cardiac Thorac & Vasc Surg, Eiveniu 2, LT-50009 Kaunas, Lithuania
关键词
bleeding; clopidogrel; dyspnea; ticagrelor; ELEVATION MYOCARDIAL-INFARCTION; ACUTE CORONARY SYNDROMES; FOCUSED UPDATE; CLOPIDOGREL; TICAGRELOR; POLYMORPHISMS; ASSOCIATION; PREVENTION; PRASUGREL; ASPIRIN;
D O I
10.2217/pgs-2018-0178
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim: The aim of this study was to determine the impact of genetic and nongenetic factors on treatment outcomes in patients receiving dual antiplatelet therapy after percutaneous coronary intervention and stent implantation. Materials &methods: Patients (n=628) used clopidogrel or ticagrelor for at least 1week before platelet aggregation test. Results: Multivariate binary regression analysis demonstrated that aspirin use and CYP4F2 T allele significantly increased odds for bleeding in clopidogrel users (OR: 2.488, 95% CI: 1.452-4.265;p=0.001and OR: 1.573, 95% CI: 1.066-2.320;respectively; p=0.022). CYP4F2 T allele significantly increased odds for bleeding in ticagrelor users (OR: 8.270, 95% CI: 3.917-17.462;p<0.001). Conclusion: Aspirin use and CYP4F2 T allele were significantly associated with bleeding during dual antiplatelet therapy.
引用
收藏
页码:483 / 492
页数:10
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