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The Kinetics of Circulating Monocyte Subsets and Monocyte-Platelet Aggregates in the Acute Phase of ST-Elevation Myocardial Infarction: Associations with 2-Year Cardiovascular Events.ST段抬高型心肌梗死急性期循环单核细胞亚群及单核细胞-血小板聚集体的动力学:与2年心血管事件的关联
Medicine (Baltimore). 2016 May;95(18):e3466. doi: 10.1097/MD.0000000000003466.
2
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3
Pharmacology of antithrombotic drugs: an assessment of oral antiplatelet and anticoagulant treatments.抗血栓药物的药理学:口服抗血小板和抗凝治疗的评估。
Lancet. 2015 Jul 18;386(9990):281-91. doi: 10.1016/S0140-6736(15)60243-4. Epub 2015 Mar 14.
4
The impact of smoking on long-term outcome of patients with premature (≤35years) ST-segment elevation acute myocardial infarction.吸烟对年龄≤35岁的ST段抬高型急性心肌梗死患者长期预后的影响。
Am Heart J. 2015 Mar;169(3):356-62. doi: 10.1016/j.ahj.2014.12.003. Epub 2014 Dec 17.
5
Effects of P2Y12 receptor inhibition in patients with ST-segment elevation myocardial infarction.ST 段抬高型心肌梗死患者的 P2Y12 受体抑制作用。
Am J Cardiol. 2014 Jun 15;113(12):2064-9. doi: 10.1016/j.amjcard.2014.03.053. Epub 2014 Apr 2.
6
Smoking and cardiovascular disease: mechanisms of endothelial dysfunction and early atherogenesis.吸烟与心血管疾病:内皮功能障碍与早期动脉粥样硬化形成的机制。
Arterioscler Thromb Vasc Biol. 2014 Mar;34(3):509-15. doi: 10.1161/ATVBAHA.113.300156.
7
Cigarette smoking and antiplatelet effects of aspirin monotherapy versus clopidogrel monotherapy in patients with atherosclerotic disease: results of a prospective pharmacodynamic study.吸烟与阿司匹林单药治疗和氯吡格雷单药治疗对动脉粥样硬化疾病患者抗血小板作用的比较:一项前瞻性药效学研究的结果
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Decreased circulating microRNA-223 level predicts high on-treatment platelet reactivity in patients with troponin-negative non-ST elevation acute coronary syndrome.循环中微小RNA-223水平降低预示肌钙蛋白阴性的非ST段抬高型急性冠状动脉综合征患者治疗期间的高血小板反应性。
J Thromb Thrombolysis. 2014 Jul;38(1):65-72. doi: 10.1007/s11239-013-1022-9.
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ST段抬高型心肌梗死后,定义高氯吡格雷血小板反应性时VASP磷酸化与血小板聚集之间的不一致性

Discordance Between VASP Phosphorylation and Platelet Aggregation in Defining High On-Clopidogrel Platelet Reactivity After ST-Segment Elevation Myocardial Infarction.

作者信息

Sun Jing, Yang Guo-Hong, Liu Jun-Xiang, Liu Xin-Lin, Ma Yong-Qiang, Lu Rui-Yi, Zhang Ying-Ying, Chen Shao-Bo, Zhao Ji-Hong, Ji Wen-Jie, Zhou Xin, Li Yu-Ming

机构信息

1 Tianjin Key Laboratory of Cardiovascular Remodeling and Target Organ Injury, Pingjin Hospital Heart Center, Tianjin, China.

The first two authors contributed equally to this work.

出版信息

Clin Appl Thromb Hemost. 2018 Jan;24(1):47-54. doi: 10.1177/1076029617726600. Epub 2017 Sep 7.

DOI:10.1177/1076029617726600
PMID:28877606
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6714637/
Abstract

To investigate potential clinical characteristics associated with discordance between platelet vasodilator-stimulated phosphoprotein phosphorylation (VASP-P) flow cytometry (FCM) assay and light transmission aggregometry (LTA) in defining high on-clopidogrel platelet reactivity (HPR) after ST-segment elevation myocardial infarction (STEMI). In this study, platelet responsiveness was measured by the above 2 methods simultaneously on day 1 and on day 6 of STEMI onset in 90 consecutive patients who underwent primary percutaneous coronary intervention. The FCM-derived platelet reactivity index and LTA-derived platelet aggregation rate were both significantly reduced after dual antiplatelet therapy on day 6. Multiple variable-adjusted logistic regression analysis revealed that smoking (odds ratio [OR]: 4.507, 95% confidence interval [CI]: 1.123-18.09, P = .034) and onset-to-admission time (per 1 hour increase, OR: 1.196, 95% CI: 1.023-1.398, P = .025) both were independent predictors for the discordance between the 2 methods. Additionally, improved correlation and concordance was observed in nonsmokers compared with smokers. Our data show that smoking and prolonged onset-to-admission time are associated with discordance between platelet VASP-P and LTA in defining HPR after STEMI, which should be considered when planning personalized antiplatelet therapy.

摘要

研究ST段抬高型心肌梗死(STEMI)后,血小板血管扩张刺激磷蛋白磷酸化(VASP-P)流式细胞术(FCM)检测与光透射聚集法(LTA)在定义高氯吡格雷血小板反应性(HPR)方面不一致的潜在临床特征。在本研究中,对90例接受直接经皮冠状动脉介入治疗的连续患者,在STEMI发病第1天和第6天同时采用上述两种方法测量血小板反应性。双联抗血小板治疗后第6天,FCM得出的血小板反应性指数和LTA得出的血小板聚集率均显著降低。多变量调整逻辑回归分析显示,吸烟(比值比[OR]:4.507,95%置信区间[CI]:1.123 - 18.09,P = .034)和发病至入院时间(每增加1小时,OR:1.196,95%CI:1.023 - 1.398,P = .025)均是两种方法不一致的独立预测因素。此外,与吸烟者相比,非吸烟者的相关性和一致性有所改善。我们的数据表明,吸烟和延长的发病至入院时间与STEMI后定义HPR时血小板VASP-P和LTA之间的不一致相关,在规划个性化抗血小板治疗时应予以考虑。