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直接凝血酶抑制剂和低分子肝素对冠心病患者血小板功能的影响:一项前瞻性干预试验。

Influence of Direct Thrombin Inhibitor and Low Molecular Weight Heparin on Platelet Function in Patients with Coronary Artery Disease: A Prospective Interventional Trial.

机构信息

Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.

Federal University of Uberlândia, Uberlândia, Brazil.

出版信息

Adv Ther. 2020 Jan;37(1):420-430. doi: 10.1007/s12325-019-01153-8. Epub 2019 Nov 22.

Abstract

INTRODUCTION

The interaction between anticoagulants and platelet function is complex. Previous publications showed mixed results regarding the role of heparins in platelet aggregation. On the other hand, the direct thrombin inhibitor (DTI) dabigatran might enhance the risk of myocardial infarction in patients with atrial fibrillation, which could be related to increased platelet aggregability.

METHODS

This was a prospective, interventional study of patients with chronic coronary artery disease (CAD) taking low-dose aspirin. The objective of the current study was to compare the effects of dabigatran versus enoxaparin on platelet aggregability. Subjects initially were on orally administered dabigatran for 5 days followed by subcutaneously administered enoxaparin after a 30-day washout period. Platelet function was assessed at baseline and after each intervention by multiple electrode aggregometry (MEA-ASPI) (primary endpoint), serum thromboxane B2 (TXB2), VerifyNow Aspirin™, and coagulation tests (secondary endpoints).

RESULTS

Compared to baseline MEA-ASPI values, dabigatran increased platelet aggregation while enoxaparin decreased platelet aggregation (+ 5 U ± 24.1 vs - 6 U ± 22.2, respectively, p = 0.012). The TXB2 assay showed the same pattern (+ 2 pg/ml for dabigatran vs - 13 pg/ml for enoxaparin, p = 0.011). None of the additional tests showed significant differences between the groups. Individually, compared to baseline TXB2 results, enoxaparin significantly decreased platelet activation [33 (16.5-95) pg/mL vs 20 (10-52) pg/mL, respectively, p = 0.026], but no significant differences were observed with dabigatran.

CONCLUSIONS

DTI and anti-Xa drugs exert opposite effects on platelet function. A significant decrease in platelet activation through COX1 (also known as prostaglandin G/H synthase 1) was observed with enoxaparin, but no significant differences in platelet function were observed with dabigatran.

TRIAL REGISTRATION

ClinicalTrials.gov identifier, NCT02389582.

摘要

简介

抗凝剂和血小板功能之间的相互作用很复杂。之前的研究结果表明肝素在血小板聚集方面的作用存在差异。另一方面,直接凝血酶抑制剂(DTI)达比加群可能会增加房颤患者发生心肌梗死的风险,这可能与血小板聚集性增加有关。

方法

这是一项前瞻性、干预性研究,纳入了正在服用低剂量阿司匹林的慢性冠状动脉疾病(CAD)患者。本研究的目的是比较达比加群和依诺肝素对血小板聚集的影响。受试者最初连续 5 天口服达比加群,然后在 30 天洗脱期后皮下注射依诺肝素。通过多重电极聚集仪(MEA-ASPI)(主要终点)、血清血栓素 B2(TXB2)、VerifyNow 阿司匹林检测试剂盒(次要终点)在基线和每次干预后评估血小板功能。

结果

与基线 MEA-ASPI 值相比,达比加群增加了血小板聚集,而依诺肝素则降低了血小板聚集(分别增加 5 U ± 24.1 和减少 6 U ± 22.2,p=0.012)。TXB2 检测结果也呈现出相同的趋势(达比加群增加 2 pg/ml,依诺肝素减少 13 pg/ml,p=0.011)。其他检测结果在两组间均无显著差异。单独来看,与基线 TXB2 结果相比,依诺肝素显著降低了血小板激活[33(16.5-95)pg/ml 比 20(10-52)pg/ml,p=0.026],但达比加群则无显著差异。

结论

DTI 和抗 Xa 药物对血小板功能的影响相反。依诺肝素通过 COX1(也称为前列腺素 G/H 合酶 1)显著降低了血小板激活,但达比加群对血小板功能无显著影响。

试验注册

ClinicalTrials.gov 标识符,NCT02389582。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3655/6979460/077f759c36e5/12325_2019_1153_Fig1_HTML.jpg

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