首页> 外文期刊>Circulation journal >Association of CYP2C19 Genotype With Periprocedural Myocardial Infarction After Uneventful Stent Implantation in Chinese Patients Receiving Clopidogrel Pretreatment
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Association of CYP2C19 Genotype With Periprocedural Myocardial Infarction After Uneventful Stent Implantation in Chinese Patients Receiving Clopidogrel Pretreatment

机译:在接受氯吡格雷预处理的中国患者植入不平衡支架后患有百血交心肌梗死的CYP2C19基因型

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Background: ?High platelet reactivity (HPR) after clopidogrel treatment is linked to an increased risk of periprocedural myocardial infarction (PMI). The occurrence of PMI that could be associated with CYP2C19 genotype status was our hypothesis. Methods and Results: ?A total of 233 patients with non-ST elevation acute coronary syndromes (NSTACS) undergoing uneventful elective percutaneous coronary intervention were included. Platelet reactivity was assessed by Thrombelastograph at 24h after 300mg clopidogrel loading. HPR was defined as ≥70% adenosine diphosphate-induced platelet aggregation. The CYP2C19*2 and *3 loss-of-function (LOF) alleles were determined using DNA microarray method. Patients with PMI had significantly higher on-clopidogrel platelet reactivity compared to those without PMI (60.0±24.4% vs. 43.0±24.0%, Padj=4.348, 95% CI: 1.846–10.241, P=0.001). Furthermore, the incidence of HPR was significantly associated with the carriage of 2 CYP2C19 LOF alleles. Compared with non-carriers, patients carrying 2 CYP2C19 LOF alleles had a 3.000-fold increased risk (95% CI: 1.071–8.400, P=0.037) for PMI in multivariate analysis. However, inclusion of HPR as a covariate in the regression model changed the significant relationship between the carriage of 2 CYP2C19 LOF alleles and PMI. Conclusions: ?Among Chinese patients with NSTACS, carriers with 2 CYP2C19 LOF alleles are more prone to HPR, which is associated with an increased risk for PMI.??(Circ J?2012; 76: 2773–2778)
机译:背景:氯吡格雷治疗后的高血小板反应性(HPR)与群体心肌梗死的风险增加(PMI)。可能与CYP2C19基因型状态相关的PMI的发生是我们的假设。方法和结果:共有233例患有经过不平缓的冠心病患者的非St升高急性冠状动脉综合征(NSTACs)。在300mg氯吡格雷加载后24小时通过血栓反应性评估血小板反应性。 HPR定义为≥70%的腺苷二磷酸诱导的血小板聚集。使用DNA微阵列方法测定CYP2C19 * 2和* 3函数损失(LOF)等位基因。与没有PMI的那些相比,PMI患者具有显着提高的氯吡格雷血小板反应性(60.0±24.4%,PADJ = 4.348,95%CI:1.846-10.241,P = 0.001)。此外,HPR的发病率与2 CYP2C19 LOF等位基因的携带显着相关。与非载体相比,携带2种CYP2C19 LOF等位基因的患者的风险增加3.000倍(95%CI:1.071-8.400,P = 0.037),用于多变量分析。然而,将HPR作为回归模型中的协变量的包装改变了2个CYP2C19 LOF等位基因和PMI的运输之间的显着关系。结论:中华患有2种CYP2C19 LOF等位基因的中国患者,携带2种CYP2C19 LOF等位基因,其与PMI的风险增加有关.?(circ j?2012; 76:2773-2778)

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