Yu Jiancai, Liu Yongxing, Peng Wanzhong, Liu Juan, Li Ya, Liu Junyan, Jiang Yang, Liu Demin, Xu Zesheng
Department of Cardiology, Teaching Hospital of Cangzhou Central Hospital of Tianjin Medical University, Tianjin Medical University, Tianjin, China.
Department of Cardiology, Cangzhou Central Hospital, Cangzhou, China.
Front Surg. 2022 Feb 9;9:839157. doi: 10.3389/fsurg.2022.839157. eCollection 2022.
To explore the influence of CYP2C19 gene combined with platelet function test on clinical prognosis of patients with complex coronary artery disease receiving antiplatelet therapy after PCI.
A total of 200 patients undergoing PCI in our hospital due to complex coronary artery disease from February 2019 to February 2021 were selected and divided into the control group and the observation group according to whether CYP2C19 gene detection was performed. The control group was treated with dual antiplatelet therapy of classical aspirin combined with clopidogrel, and the observation group was treated with individual antiplatelet therapy. The patients in the two groups were followed up for 1 year after PCI, and their quality of life was assessed using the Seattle Angina Questionnaire (SAQ score). The occurrence of major adverse cardiovascular events (MACE) during the follow-up period was also recorded.
The incidence of total MACE events in the observation group was slightly less than that in the control group, and the difference was statistically significant ( = 0.040). In particular, the observation group was superior to the control group in reducing the readmission rate of recurrent unstable angina pectoris, and the difference was statistically significant ( = 0.023). The location of coronary culprit lesions with recurrent ischemic events was commonly seen in non-interventional target lesions (interventional/non-interventional target sites: 12.9%: 77.1%). The SAQ score in the observation group was larger than that in the control group, and the difference was statistically significant ( = 0.012). There was no statistical difference in the incidence of major bleeding between the two groups ( = 0.352).
Using CYP2C19 genotype combined with platelet function test to guide individualized antiplatelet therapy after complex coronary artery PCI is beneficial to reducing ischemic events in a short period (1 year), mainly due to reducing the risk of readmission for recurrent unstable angina pectoris, and improving the quality of daily life of patients without increasing the risk of massive hemorrhage, which can improve clinical prognosis.
探讨CYP2C19基因联合血小板功能检测对复杂冠状动脉疾病患者PCI术后抗血小板治疗临床预后的影响。
选取2019年2月至2021年2月在我院因复杂冠状动脉疾病接受PCI治疗的200例患者,根据是否进行CYP2C19基因检测分为对照组和观察组。对照组采用经典阿司匹林联合氯吡格雷双重抗血小板治疗,观察组采用个体化抗血小板治疗。两组患者PCI术后随访1年,采用西雅图心绞痛问卷(SAQ评分)评估其生活质量。记录随访期间主要不良心血管事件(MACE)的发生情况。
观察组MACE事件总发生率略低于对照组,差异有统计学意义(=0.040)。尤其是观察组在降低复发性不稳定型心绞痛再入院率方面优于对照组,差异有统计学意义(=0.023)。复发性缺血事件的冠状动脉罪犯病变部位常见于非介入靶病变(介入/非介入靶部位:12.9%:77.1%)。观察组SAQ评分高于对照组,差异有统计学意义(=0.012)。两组大出血发生率差异无统计学意义(=0.352)。
采用CYP2C19基因分型联合血小板功能检测指导复杂冠状动脉PCI术后个体化抗血小板治疗,有利于短期内(1年)降低缺血事件,主要是降低复发性不稳定型心绞痛再入院风险,提高患者日常生活质量,且不增加大出血风险,可改善临床预后。