The impact of CYP3A5*1/*3, PIA1/A2 and T744C polymorphisms on clopidogrel and acetylsalicylic acid response variability in Mexican population

被引:9
|
作者
Isordia-Salas, Irma [1 ]
Jaciel Olalde-Roman, Marcos [2 ]
Santiago-German, David [1 ,3 ]
Corona de la Pena, Norma [1 ]
Salvador Valencia-Sanchez, Jesus [2 ]
机构
[1] HGR 1 Dr Carlos Mac Gregor Sanchez Navarro Inst M, Unidad Invest Med Trombosis Hemostasia & Aterogen, Mexico City, DF, Mexico
[2] Hosp Cardiol, Inst Mexicano Seguro Social, Ctr Med Nacl Siglo 21, Unidad Cuidados Intens Cardiovasc, Mexico City, DF, Mexico
[3] Inst Politecn Nacl, Escuela Nacl Ciencias Biol, Mexico City, DF, Mexico
关键词
Clopidogrel; Acetylsalicylic; Platelets; Polymorphism; ACUTE CORONARY SYNDROME; ACUTE MYOCARDIAL-INFARCTION; PLATELET REACTIVITY; ATHEROTHROMBOTIC EVENTS; GENETIC POLYMORPHISMS; HEALTHY-SUBJECTS; INCREASED RISK; RESISTANCE; ASPIRIN; P2Y(12);
D O I
10.1016/j.thromres.2012.06.024
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Clopidogrel is recommended in addition to aspirin to prevent atherothrombotic events in patients with acute coronary syndromes (ACS) and in those undergoing percutaneous coronary intervention (PCI). However, an interindividual variability in platelet inhibition response to clopidogrel has been demonstrated, and is associated with recurrent cardiovascular events. Multiple mechanisms have been associated with no response including genetics factors. Materials and methods: The present study enrolled 60 patients with ACS undergoing emergent PCI. Platelet aggregation to adenosine diphosphate and arachidonic acid was assessed by turbidimetric method at 24 hours after dual administration of 300 mg of clopidogrel and 300 mg of acetylsalicylic acid loading dose. Clopidogrel or acetylsalicylic acid resistance was defined by persistence of Platelet Reactivity (PR = ADP-Ag >70% or PR = Arachidonic Acid-Ag>20%) respectively. The CYP3A51*/5*, PIA1/A2, and T744C polymorphisms were determined in all participants by PCR-RFLP. Results: The allelic frequencies were: CYP3A5*3 (71.65%), PIA2 (10.8%), and 744 C (15.0%). We founded high percent of clopidogrel resistance (60.0%), compared with 8.3% of acetylsalicylic acid in those patients. The genotype frequencies of those polymorphisms were similar between responders and non responders defined by PR. There was a high percent of coronary adverse events. Conclusions: We identified a high percent of clopidogrel resistance in Mexican patients with ACS undergoing PCI. However, a normal platelet response to acetylsalicylic acid was observed in most of them. There was no association between CYP3A5*1/*3, PIA1/A2, and T744C polymorphisms and clopidogrel resistance. More studies are needed to determine the possible interaction between genetics factors, platelet response to clopidogrel and cardiovascular adverse events. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:E67 / E72
页数:6
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