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CYP2C19基因检测在中国人群中指导抗血小板治疗的临床价值

Clinical Value of CYP2C19 Genetic Testing for Guiding the Antiplatelet Therapy in a Chinese Population.

作者信息

Shen De-Liang, Wang Bo, Bai Jing, Han Qing, Liu Chuang, Huang Xiao-Hui, Zhang Jin-Ying

机构信息

Department of Cardiology, The First Affiliated Hospital of Zhengzhou University, Henan Province, China.

出版信息

J Cardiovasc Pharmacol. 2016 Mar;67(3):232-6. doi: 10.1097/FJC.0000000000000337.

Abstract

OBJECTIVE

To compare the clinical effects between individual antiplatelet therapy guided by CYP2C19 genetic testing and conventional dual antiplatelet therapy in patients with coronary artery disease after percutaneous coronary intervention.

METHODS

In total of 628 coronary artery disease patients who had undergone successful percutaneous coronary intervention were included in this study. Patients were consecutively divided into routine group (n = 319) and individual group (n = 309) because of weather received CYP2C19 genetic testing. The individual group was divided again into extensive metabolizer group, intermediate metabolizer group, and poor metabolizer group according to CYP2C19 genotype. Then extensive metabolizer group received 75 mg daily of clopidogrel, intermediate metabolizer group received 150 mg daily of clopidogrel, and poor metabolizer group received ticagrelor 90 mg twice daily. Routine group was treated with clopidogrel 75 mg daily conventionally. The primary end points were defined as major adverse cardiovascular events (MACE), namely a composite of death from any cause, myocardial infarction, or target vessel revascularization. Safety end points were bleeding events classified by GUSTO.

RESULTS

All the 628 patients were followed for an average of 12 months and clinical outcomes were analyzed at 1, 6, and 12 months after discharge. The morbidity rates of MACE in individual group were all lower than those in routine group at 1, 6, and 12 months (1.3% vs. 5.6%, P = 0.003; 3.2% vs. 7.8%, P = 0.012; 4.2% vs. 9.4%, P = 0.010). No significant difference in the rates of bleeding was found between the 2 groups (P > 0.05). Even performed a multivariate logistic regression analysis, the benefit of individual antiplatelet therapy remained.

CONCLUSION

Individual antiplatelet therapy guided by CYP2C19 genetic testing significantly reduced the rate of MACE without an increase in the rate of bleeding in the near term in this Chinese population.

摘要

目的

比较经皮冠状动脉介入治疗后冠心病患者中,CYP2C19基因检测指导下的个体化抗血小板治疗与传统双联抗血小板治疗的临床效果。

方法

本研究纳入了628例成功接受经皮冠状动脉介入治疗的冠心病患者。根据是否接受CYP2C19基因检测,患者连续分为常规组(n = 319)和个体化组(n = 309)。个体化组再根据CYP2C19基因型分为快代谢组、中代谢组和慢代谢组。然后,快代谢组每日服用75 mg氯吡格雷,中代谢组每日服用150 mg氯吡格雷,慢代谢组每日两次服用替格瑞洛90 mg。常规组常规每日服用75 mg氯吡格雷。主要终点定义为主要不良心血管事件(MACE),即任何原因导致的死亡、心肌梗死或靶血管血运重建的复合事件。安全性终点为根据GUSTO分类的出血事件。

结果

628例患者平均随访12个月,并在出院后1、6和12个月分析临床结局。个体化组在1、6和12个月时的MACE发病率均低于常规组(1.3%对5.6%,P = 0.003;3.2%对7.8%,P = 0.012;4.2%对9.4%,P = 0.010)。两组间出血率无显著差异(P > 0.05)。即使进行多因素逻辑回归分析,个体化抗血小板治疗的益处仍然存在。

结论

在中国人群中,CYP2C19基因检测指导下的个体化抗血小板治疗在近期显著降低了MACE发生率,且未增加出血率。

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