CYP2C19 基因型与冠状动脉搭桥术后心房颤动的关系。

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Qin Jiang, Keli Huang, Lizhu Han, Hong Kong, Zhenglin Yang, Shengshou Hu
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引用次数: 0

摘要

这项队列研究旨在评估细胞色素P450家族2亚家族C成员19(CYP2C19)基因分型、口服氯吡格雷后的血小板聚集性以及非体外循环冠状动脉旁路移植术(CABG)术后心房颤动(POAF)发生率之间的联系。从2017年5月至2022年11月,共纳入258名接受择期首次CABG手术的患者进行分析,这些患者术后接受100毫克/天的口服阿司匹林和75毫克/天的口服氯吡格雷治疗。这些患者根据 CYP2C19 基因分型进行分类。在 CABG 术前、术后 1 天和 5 天以及出院前,使用多电极聚集测定法连续评估血小板聚集性。采用累积风险对数秩检验比较了 POAF 的发生率。CYP2C19基因分型将患者分为CYP2C19*1*1组(WT组,n = 123)和CYP2C19*2或*3组(LOF组,n = 135)。两组的基线特征和手术数据无明显差异。LOF 组 CABG 术后 POAF 的发生率为 42.2%,而 WT 组为 22.8%(危险风险 [HR]:2.061;95% 置信区间 [CI]:1.347, 3.15%):1.347, 3.153; p = 0.0013).CABG 术后 5 天,LOF 组的二磷酸腺苷刺激血小板聚集明显高于 WT 组(30.4% ± 6.5% vs. 17.9% ± 4.1%,P = 0.0013)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association of CYP2C19 genotypes with postoperative atrial fibrillation after coronary artery bypass surgery

Association of CYP2C19 genotypes with postoperative atrial fibrillation after coronary artery bypass surgery

This cohort study aims to assess the connection between cytochrome P450 family 2 subfamily C member 19 (CYP2C19) genotyping, platelet aggregability following oral clopidogrel administration, and the occurrence of postoperative atrial fibrillation (POAF) after off-pump coronary artery bypass graft (CABG) surgery. From May 2017 to November 2022, a total of 258 patients undergoing elective first-time CABG surgery, receiving 100 mg/day oral aspirin and 75 mg/day oral clopidogrel postoperatively, was included for analysis. These patients were categorized based on CYP2C19 genotyping. Platelet aggregability was assessed serially using multiple-electrode aggregometry before CABG, 1 and 5 days after the procedure, and before discharge. The incidences of POAF were compared using the log-rank test for cumulative risk. CYP2C19 genotyping led to categorization into CYP2C19*1*1 (WT group, n = 123) and CYP2C19*2 or *3 (LOF group, n = 135). Baseline characteristics and operative data showed no significant differences between the two groups. The incidence of POAF after CABG was 42.2% in the LOF group, contrasting with 22.8% in the WT group (hazard risk [HR]: 2.061; 95% confidence interval [CI]: 1.347, 3.153; p = 0.0013). Adenosine diphosphate-stimulated platelet aggregation was notably higher in the LOF group compared to the WT group 5 days after CABG (30.4% ± 6.5% vs. 17.9% ± 4.1%, p < 0.001), remaining a similar higher level at hospital discharge (25.6% ± 6.1% vs. 12.2% ± 3.5%, p < 0.001). The presence of CYP2C19 LOF was linked to a higher incidence of POAF and relatively elevated platelet aggregation after CABG surgery under the same oral clopidogrel regimen.

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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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