Chen Yu-Wei, Liao Yi-Ju, Chang Wei-Chun, Hsiao Tzu-Hung, Lin Ching-Heng, Hsu Chiann-Yi, Liu Tsun-Jui, Lee Wen-Lieng, Chen Yi-Ming
Cardiovascular Center, Taichung Veterans General Hospital, Taichung, Taiwan.
Institute of Clinical Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Front Cardiovasc Med. 2022 Aug 22;9:994184. doi: 10.3389/fcvm.2022.994184. eCollection 2022.
CYP2C19 loss-of-function (LOF) alleles reduce the effectiveness of clopidogrel and are associated with high rates of clinical events in patients undergoing percutaneous coronary intervention (PCI) and stenting in Northeast Asians. However, the prevalence and influence of CYP2C19 LOF alleles in Southeast Asians remain unclear.
This study aims to retrospectively investigate the prevalence of CYP2C19 LOF alleles and clinical outcomes in East Asian patients taking clopidogrel and undergoing PCI.
Between June 2019 and June 2020, volunteer participants in a single medical center were consecutively selected. The genetic data of CYP2C19 were derived from the Taiwan Precision Medicine Initiative (TPMI). Patients receiving clopidogrel while undergoing PCI with stenting were retrospectively analyzed.
A total of 999 patients (62.4 ± 11.1 years old, 83.7% men) were enrolled; 39.3% without the CYP2C19 LOF allele (normal metabolizers + rapid metabolizers, NM + RM); 44.9% with one LOF allele (intermediate metabolizers, IM); 15.7% with two LOF alleles (poor metabolizers, PM). The incidence of stroke was higher in the PM subgroup compared to the NM + RM subgroup or IM subgroup in patients presenting with acute myocardial infarction (AMI). The 1-year major adverse cardiac and cerebrovascular events (MACCE)-free survival rates in all participants were similar among the three groups. However, in the AMI group, the 1-year MACCE-free survival rates were significantly lower in the PM subgroup compared to the NM + RM subgroup or IM subgroup.
In East Asians presenting with AMI, CYP2C19 PM was associated with deleterious cardiovascular outcomes and stroke. Our results reinforce the crucial role of preemptive CYP2C19 genotyping in East Asian AMI patients receiving clopidogrel treatment.
细胞色素P450 2C19(CYP2C19)功能缺失(LOF)等位基因会降低氯吡格雷的疗效,并且与东北亚地区接受经皮冠状动脉介入治疗(PCI)和支架植入术的患者发生临床事件的高发生率相关。然而,CYP2C19 LOF等位基因在东南亚人群中的流行情况及其影响仍不清楚。
本研究旨在回顾性调查服用氯吡格雷并接受PCI的东亚患者中CYP2C19 LOF等位基因的流行情况及临床结局。
在2019年6月至2020年6月期间,连续选取了一家医疗中心的志愿者参与者。CYP2C19的基因数据来自台湾精准医学计划(TPMI)。对接受氯吡格雷治疗并同时接受PCI及支架植入术的患者进行回顾性分析。
共纳入999例患者(年龄62.4±11.1岁,男性占83.7%);39.3%无CYP2C19 LOF等位基因(正常代谢者+快速代谢者,NM+RM);44.9%有一个LOF等位基因(中间代谢者,IM);15.7%有两个LOF等位基因(慢代谢者,PM)。在急性心肌梗死(AMI)患者中,PM亚组的卒中发生率高于NM+RM亚组或IM亚组。三组参与者的1年无主要不良心脑血管事件(MACCE)生存率相似。然而,在AMI组中,PM亚组的1年无MACCE生存率显著低于NM+RM亚组或IM亚组。
在患有AMI的东亚人群中,CYP2C19慢代谢与有害的心血管结局及卒中相关。我们的结果强化了在接受氯吡格雷治疗的东亚AMI患者中进行CYP2C19基因分型的关键作用。