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首页> 外文期刊>International journal of clinical pharmacy. >Distribution of CYP2C19 polymorphisms in Mongolian and Han nationals and the choice of specific antiplatelet drugs
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Distribution of CYP2C19 polymorphisms in Mongolian and Han nationals and the choice of specific antiplatelet drugs

机译:Cyp2C19在蒙古族和汉族多态性的分布及特定抗血小板药物的选择

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Background Individualized medication reviews may improve our understanding of the distribution of CYP2C19 polymorphisms in ethnic populations. Objective To evaluate differences in CYP2C19 gene polymorphisms between Mongolian and Han nationals and determine the effect of adjustments of antiplatelet treatments according to the genetic profile in patients undergoing percutaneous coronary intervention (PCI). Setting Prospective, observational, single-center study. Methods 397 patients diagnosed with acute coronary syndrome were enrolled. Additionally, 186 patients undergoing PCI were given different treatments according to their CYP2C19 genotypes. Patients with the genotype of an extensive metabolizers (EMs; *1/*1) were co-administered aspirin 100 mg/day and clopidogrel 75 mg/day, following a loading dose of 300 mg; intermediate metabolizers (IMs; e.g., *1/*2 and *1/*3) and poor metabolizers (PMs; e.g., *2/*2 and *2/*3) were administered a loading dose of 180 mg ticagrelor, followed by a maintenance dose of 90 mg twice a day. Results In Mongolians, 60.79% of patients were EMs, which was significantly higher than that in Han nationals (P = 0.002). In Han individuals, 62.14% of patients were IMs and PMs, which was significantly higher than that in Mongolians (P < 0.05). Three patients died, and the frequency of adverse events during follow-up was significantly higher in patients given conventional treatment than in patients given tailored treatment (P = 0.039). However, differences in metabolism subtypes did not affect the incidence of adverse reactions. Conclusions There were differences in CYP2C19 polymorphisms between Mongolians and Hans. Effective, safe therapy was achieved by tailoring antiplatelet drug therapy based on genotype.
机译:背景技术个性化药物评论可能会改善我们对民族人群中CYP2C19多态性分布的理解。目的评价蒙古族和汉族的CYP2C19基因多态性差异,并确定抗血小板治疗调整术后经皮冠状动脉介入(PCI)的遗传概况。设定前瞻性,观测,单中心研究。方法注册了397例患有急性冠状动脉综合征的患者。此外,根据其CYP2C19基因型,给予接受PCI的186名患者。患有广泛代谢剂(EMS; * 1 / * 1)的基因型(EMS; * 1 / * 1)是共同施用的阿司匹林100mg /天和氯吡格雷75mg /天,按负载剂量为300mg;中间代谢剂(IMS;例如,* 1 / * 2和* 1 / * 3)和差的代谢剂(PMS;例如,* 2 / * 2和* 2 / * 3)被施用180mg TicagreloRoS的负载剂量通过每天两次维持剂量为90毫克。结果蒙古人,60.79%的患者是EMS,其显着高于汉族(P = 0.002)。在汉族人中,62.14%的患者是IMS和PMS,其显着高于蒙古人(P <0.05)。三名患者死亡,常规治疗患者的随访期间的不良事件频率显着高于给予定制治疗的患者(P = 0.039)。然而,新陈代谢亚型的差异不会影响不良反应的发生率。结论蒙古族与汉斯科技园区CYP2C19多态性存在差异。通过基于基因型定制抗血小板药物治疗来实现有效的安全疗法。

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