I. Grazhdankin, A. Prokhorikhin, V. Baystrukov, E. Kretov, A. M. Chernyavskiy, V. Lukinov
{"title":"随访 60 个月期间 CYP2C19 基因多态性对心肌梗死患者临床预后的影响","authors":"I. Grazhdankin, A. Prokhorikhin, V. Baystrukov, E. Kretov, A. M. Chernyavskiy, V. Lukinov","doi":"10.21688/1681-3472-2023-4-64-76","DOIUrl":null,"url":null,"abstract":"Objective: To evaluate the effect of CYP2C19 gene polymorphisms on clinical outcomes in patients after successful revascularization for acute myocardial infarction with and without ST segment elevation during clopidogrel therapy for 60 months of follow-up.Methods: From 2011 to 2012, 363 patients with acute myocardial infarction who underwent coronary revascularization were included in the study. In the postoperative period, the patients underwent genetic analysis for the CYP2C19 gene polymorphism. All patients received dual antiplatelet therapy with aspirin and clopidogrel. The 60-month follow-up period assessed the primary composite endpoint of the cumulative incidence of all-cause mortality, recurrent myocardial infarction, and stroke.Results: At 60 months after the initial intervention, 71 patients had a composite primary endpoint event (all-cause death, recurrent myocardial infarction, or stroke): 50 (20%, 95% CI 16–25) in the group patients with \"wild genotype\" and 21 patients of the \"loss of function (LOF) *2+*3\" group (19%, 95% CI 13–27). No significant relationship was observe between carriage of LOF alleles of the CYP2C19 and the primary endpoint during the 60-month follow-up (HR 0.99, 95% CI 0.59–1.65, P = .965), as well as between carriage of the homozygous CYP2C19 variant (*2/*2) and the development of myocardial infarction during the same period (HR 1.26, 95% CI 0.30–5.20, P = .752).Conclusion: No correlation was observed between the CYP2C19 gene polymorphisms (*2, *3 alleles) and the incidence of ischemic events in patients with myocardial infarction after myocardial revascularization throughout a 60-month follow-up period. Received 27 November 2022. Revised 25 September 2023. Accepted 26 September 2023. Funding: The study did not have sponsorship. Conflict of interest: The authors declare no conflict of interest. Contribution of the authorsConception and study design: I.O. GrazhdankinData collection and analysis: I.O. GrazhdankinStatistical analysis: V.L. LukinovDrafting the article: I.O. Grazhdankin, A.A. Prokhorikhin, V.I. Baystrukov, E.I. Kretov, V.L. LukinovCritical revision of the article: A.M. ChernyavskiyFinal approval of the version to be published: I.O. Grazhdankin, A.A. Prokhorikhin, V.I. Baystrukov, E.I. Kretov, A.M. Chernyavskiy, V.L. Lukinov","PeriodicalId":19853,"journal":{"name":"Patologiya krovoobrashcheniya i kardiokhirurgiya","volume":"9 20","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Impact of CYP2C19 gene polymorphisms on clinical outcomes in patients with myocardial infarction during 60 months of follow-up\",\"authors\":\"I. Grazhdankin, A. Prokhorikhin, V. Baystrukov, E. Kretov, A. M. Chernyavskiy, V. Lukinov\",\"doi\":\"10.21688/1681-3472-2023-4-64-76\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective: To evaluate the effect of CYP2C19 gene polymorphisms on clinical outcomes in patients after successful revascularization for acute myocardial infarction with and without ST segment elevation during clopidogrel therapy for 60 months of follow-up.Methods: From 2011 to 2012, 363 patients with acute myocardial infarction who underwent coronary revascularization were included in the study. In the postoperative period, the patients underwent genetic analysis for the CYP2C19 gene polymorphism. All patients received dual antiplatelet therapy with aspirin and clopidogrel. The 60-month follow-up period assessed the primary composite endpoint of the cumulative incidence of all-cause mortality, recurrent myocardial infarction, and stroke.Results: At 60 months after the initial intervention, 71 patients had a composite primary endpoint event (all-cause death, recurrent myocardial infarction, or stroke): 50 (20%, 95% CI 16–25) in the group patients with \\\"wild genotype\\\" and 21 patients of the \\\"loss of function (LOF) *2+*3\\\" group (19%, 95% CI 13–27). No significant relationship was observe between carriage of LOF alleles of the CYP2C19 and the primary endpoint during the 60-month follow-up (HR 0.99, 95% CI 0.59–1.65, P = .965), as well as between carriage of the homozygous CYP2C19 variant (*2/*2) and the development of myocardial infarction during the same period (HR 1.26, 95% CI 0.30–5.20, P = .752).Conclusion: No correlation was observed between the CYP2C19 gene polymorphisms (*2, *3 alleles) and the incidence of ischemic events in patients with myocardial infarction after myocardial revascularization throughout a 60-month follow-up period. Received 27 November 2022. Revised 25 September 2023. Accepted 26 September 2023. Funding: The study did not have sponsorship. Conflict of interest: The authors declare no conflict of interest. Contribution of the authorsConception and study design: I.O. GrazhdankinData collection and analysis: I.O. GrazhdankinStatistical analysis: V.L. LukinovDrafting the article: I.O. Grazhdankin, A.A. 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引用次数: 0
摘要
目的评估CYP2C19基因多态性对在氯吡格雷治疗60个月的随访期间,因急性心肌梗死成功接受血管再通手术后伴有或不伴有ST段抬高的患者临床预后的影响:2011年至2012年,363名急性心肌梗死患者接受了冠状动脉血运重建手术。术后,患者接受了 CYP2C19 基因多态性的遗传分析。所有患者都接受了阿司匹林和氯吡格雷双重抗血小板治疗。随访期为60个月,评估的主要复合终点是全因死亡率、复发性心肌梗死和中风的累积发生率:结果:在首次干预后的 60 个月,71 名患者发生了复合主要终点事件(全因死亡、复发性心肌梗死或中风):野生基因型 "组 50 人(20%,95% CI 16-25),"功能缺失(LOF)*2+*3 "组 21 人(19%,95% CI 13-27)。在60个月的随访中,未观察到CYP2C19的LOF等位基因携带与主要终点之间有明显关系(HR 0.99,95% CI 0.59-1.65,P = .965),也未观察到同型CYP2C19变体(*2/*2)携带与同期心肌梗死发生之间有明显关系(HR 1.26,95% CI 0.30-5.20,P = .752):结论:在60个月的随访期内,未观察到CYP2C19基因多态性(*2、*3等位基因)与心肌梗死患者心肌血管重建后缺血性事件的发生率之间存在相关性。2022 年 11 月 27 日收到。2023年9月25日修订。2023年9月26日接受。资助:本研究未获得赞助。利益冲突:作者声明无利益冲突。作者贡献构思与研究设计:I.O. GrazhdankinI.O. Grazhdankin 数据收集与分析:I.O. Grazhdankin数据收集和分析:I.O. Grazhdankin 统计分析:V.L. LukinovV.L. Lukinov起草文章:I.O. Grazhdankin、A.A. Prokhorikhin、V.I. Baystrukov、E.I. Kretov、V.L. LukinovCritical revision of the article:A.M. ChernyavskiyFinal approval of the version to be published:I.O. Grazhdankin, A.A. Prokhorikhin, V.I. Baystrukov, E.I. Kretov, A.M. Chernyavskiy, V.L. Lukinov
Impact of CYP2C19 gene polymorphisms on clinical outcomes in patients with myocardial infarction during 60 months of follow-up
Objective: To evaluate the effect of CYP2C19 gene polymorphisms on clinical outcomes in patients after successful revascularization for acute myocardial infarction with and without ST segment elevation during clopidogrel therapy for 60 months of follow-up.Methods: From 2011 to 2012, 363 patients with acute myocardial infarction who underwent coronary revascularization were included in the study. In the postoperative period, the patients underwent genetic analysis for the CYP2C19 gene polymorphism. All patients received dual antiplatelet therapy with aspirin and clopidogrel. The 60-month follow-up period assessed the primary composite endpoint of the cumulative incidence of all-cause mortality, recurrent myocardial infarction, and stroke.Results: At 60 months after the initial intervention, 71 patients had a composite primary endpoint event (all-cause death, recurrent myocardial infarction, or stroke): 50 (20%, 95% CI 16–25) in the group patients with "wild genotype" and 21 patients of the "loss of function (LOF) *2+*3" group (19%, 95% CI 13–27). No significant relationship was observe between carriage of LOF alleles of the CYP2C19 and the primary endpoint during the 60-month follow-up (HR 0.99, 95% CI 0.59–1.65, P = .965), as well as between carriage of the homozygous CYP2C19 variant (*2/*2) and the development of myocardial infarction during the same period (HR 1.26, 95% CI 0.30–5.20, P = .752).Conclusion: No correlation was observed between the CYP2C19 gene polymorphisms (*2, *3 alleles) and the incidence of ischemic events in patients with myocardial infarction after myocardial revascularization throughout a 60-month follow-up period. Received 27 November 2022. Revised 25 September 2023. Accepted 26 September 2023. Funding: The study did not have sponsorship. Conflict of interest: The authors declare no conflict of interest. Contribution of the authorsConception and study design: I.O. GrazhdankinData collection and analysis: I.O. GrazhdankinStatistical analysis: V.L. LukinovDrafting the article: I.O. Grazhdankin, A.A. Prokhorikhin, V.I. Baystrukov, E.I. Kretov, V.L. LukinovCritical revision of the article: A.M. ChernyavskiyFinal approval of the version to be published: I.O. Grazhdankin, A.A. Prokhorikhin, V.I. Baystrukov, E.I. Kretov, A.M. Chernyavskiy, V.L. Lukinov