Leon H. Charney Division of Cardiology and Center for the Prevention of Cardiovascular Disease, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Division of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Curr Cardiol Rep. 2024 May;26(5):423-434. doi: 10.1007/s11886-024-02049-y. Epub 2024 Apr 4.
Targeting traditional cardiovascular risk factors is effective in reducing recurrent cardiovascular events, yet the presence of residual cardiovascular risk due to underlying systemic inflammation is a largely unaddressed opportunity. This review aims to comprehensively assess the evolving role of colchicine as a therapeutic approach targeting residual inflammatory risk in the context of those with coronary artery disease (CAD).
Inflammation plays a significant role in promoting atherosclerosis, and targeting anti-inflammatory pathways has the potential to decrease cardiovascular events. Low-dose colchicine (0.5 mg/day orally), when added to guideline-directed medical care for CAD, safely decreases major adverse cardiovascular events (MACE) by 31% in stable atherosclerosis patients and 23% in those after recent myocardial infarctions. Meta-analyses of recent randomized control trials further support both the efficacy and safety of colchicine, particularly when added to other standard cardiovascular therapies, including statin therapy. The European Society of Cardiology and other national guidelines endorse the use of low-dose colchicine in patients across the spectrum of CAD. Recently, colchicine was FDA-approved in the United States as the first anti-inflammatory therapy for the reduction of cardiovascular events. In a period of a rising incidence of CAD across the globe, colchicine represents a unique opportunity to decrease MACE due to its large magnitude of benefits and general affordability. However, challenges with drug interactions must be addressed, especially in those regions where HIV, hepatitis, and tuberculosis are prevalent. Colchicine is safe and effective at reducing cardiovascular events across a broad spectrum of coronary syndromes. The ability to simultaneously target traditional risk factors and mitigate residual inflammatory risk marks a substantial advancement in cardiovascular prevention strategies, heralding a new era in the global battle against CAD.
针对传统心血管危险因素进行干预可有效降低心血管事件再发风险,但由于潜在的系统性炎症,仍存在大量未得到解决的心血管残余风险。本综述旨在全面评估秋水仙碱在冠心病(CAD)患者中作为一种针对残余炎症风险的治疗方法的作用。
炎症在促进动脉粥样硬化方面起着重要作用,靶向抗炎途径有可能降低心血管事件的发生风险。小剂量秋水仙碱(每天 0.5mg 口服)在 CAD 指南指导的药物治疗基础上,可使稳定型动脉粥样硬化患者的主要不良心血管事件(MACE)降低 31%,近期心肌梗死后患者的 MACE 降低 23%。最近的随机对照试验的荟萃分析进一步支持了秋水仙碱的疗效和安全性,尤其是当与其他标准心血管治疗方法(包括他汀类药物治疗)联合使用时。欧洲心脏病学会和其他国家的指南都支持在 CAD 患者中使用小剂量秋水仙碱。最近,秋水仙碱在美国获得 FDA 批准,成为第一种用于降低心血管事件的抗炎治疗药物。在全球 CAD 发病率不断上升的时期,秋水仙碱因其疗效显著且价格合理,为降低 MACE 提供了一个独特的机会。然而,必须解决药物相互作用的问题,尤其是在 HIV、肝炎和结核病流行的地区。秋水仙碱在广泛的冠状动脉综合征中安全有效,可降低心血管事件的发生风险。同时针对传统危险因素和减轻残余炎症风险的能力标志着心血管预防策略的重大进展,预示着全球对抗 CAD 的新的时代的到来。