Division of Cardiology, A.O.U. Policlinico "G. Rodolico-San Marco," University of Catania, Italy (D.C.).
Division of Cardiology, University of Florida College of Medicine, Jacksonville (D.J.A.).
Circulation. 2020 Dec;142(22):2172-2188. doi: 10.1161/CIRCULATIONAHA.120.045465. Epub 2020 Nov 30.
Patients with diabetes mellitus (DM) are characterized by enhanced thrombotic risk attributed to multiple mechanisms including hyperreactive platelets, hypercoagulable status, and endothelial dysfunction. As such, they are more prone to atherosclerotic cardiovascular events than patients without DM, both before and after coronary artery disease (CAD) is established. In patients with DM without established CAD, primary prevention with aspirin is not routinely advocated because of its increased risk of major bleeding that largely offsets its ischemic benefit. In patients with DM with established CAD, secondary prevention with antiplatelet drugs is an asset of pharmacological strategies aimed at reducing the risk of atherosclerotic cardiovascular events and their adverse prognostic consequences. Such antithrombotic strategies include single antiplatelet therapy (eg, with aspirin or a P2Y inhibitor), dual antiplatelet therapy (eg, aspirin combined with a P2Y inhibitor), and dual-pathway inhibition (eg, aspirin combined with the vascular dose of the direct oral anticoagulant rivaroxaban) for patients with chronic ischemic heart disease, acute coronary syndromes, and those undergoing percutaneous coronary intervention. Because of their increased risk of thrombotic complications, patients with DM commonly achieve enhanced absolute benefit from more potent antithrombotic approaches compared with those without DM, which most often occurs at the expense of increased bleeding. Nevertheless, studies have shown that when excluding individuals at high risk for bleeding, the net clinical benefit favors the use of intensified long-term antithrombotic therapy in patients with DM and CAD. Several studies are ongoing to establish the role of novel antithrombotic strategies and drug formulations in maximizing the net benefit of antithrombotic therapy for patients with DM. The scope of this review article is to provide an overview of current and evolving antithrombotic strategies for primary and secondary prevention of atherosclerotic cardiovascular events in patients with CAD and DM.
糖尿病(DM)患者的血栓形成风险增强,其机制包括反应过度的血小板、高凝状态和内皮功能障碍。因此,与无 DM 的患者相比,他们在发生冠状动脉疾病(CAD)之前和之后更容易发生动脉粥样硬化心血管事件。对于没有确诊 CAD 的 DM 患者,由于其大出血风险增加,而缺血获益基本抵消,因此不常规推荐使用阿司匹林进行一级预防。对于已经确诊 CAD 的 DM 患者,抗血小板药物的二级预防是旨在降低动脉粥样硬化心血管事件及其不良预后后果风险的药物治疗策略的一个组成部分。这些抗血栓形成策略包括单药抗血小板治疗(例如,使用阿司匹林或 P2Y 抑制剂)、双联抗血小板治疗(例如,阿司匹林联合 P2Y 抑制剂)和双途径抑制(例如,阿司匹林联合直接口服抗凝剂利伐沙班的血管剂量),适用于慢性缺血性心脏病、急性冠状动脉综合征和接受经皮冠状动脉介入治疗的患者。由于血栓形成并发症风险增加,与无 DM 的患者相比,DM 患者通常从更有效的抗血栓形成方法中获得更大的绝对获益,这通常是以增加出血为代价的。然而,研究表明,在排除大出血风险高的个体后,强化长期抗血栓形成治疗有利于 DM 和 CAD 患者。目前正在进行几项研究,以确定新型抗血栓形成策略和药物制剂在为 DM 患者最大化抗血栓形成治疗的净临床获益方面的作用。本文的范围是提供对 CAD 和 DM 患者动脉粥样硬化心血管事件一级和二级预防中当前和不断发展的抗血栓形成策略的概述。