Emory Clinical Cardiovascular Research Institute, Division of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Health Policy, Quality & Informatics Program, Michael E. DeBakey Veterans Affairs Medical Center Health Services Research and Development Center for Innovations, Houston, TX, USA.
Curr Atheroscler Rep. 2020 Jan 11;22(1):3. doi: 10.1007/s11883-020-0822-6.
This review highlights selected cardiovascular disease (CVD) prevention studies presented at the 2019 American Heart Association (AHA) Scientific Sessions.
Several important cardiovascular prevention studies were presented at the 2019 AHA Scientific Sessions. Results from the Colchicine Cardiovascular Outcomes Trial (COLCOT) showed that low-dose colchicine reduces the risk of recurrent CVD events among patients with recent myocardial infarction. A prospective analysis from the UK Biobank cohort demonstrated that the increased CVD risk associated with clonal hematopoiesis of indeterminate potential is mitigated by a common disruptive mutation in the IL6R gene that suppresses the pro-inflammatory IL-1β/IL-6 pathway. The Treat Stroke to Target trial demonstrated that reducing low-density lipoprotein cholesterol to <70 mg/dL among patients with ischemic stroke or transient ischemic attack reduces the risk of recurrent CVD events as compared with a higher LDL-C target of 90-110 mg/dL. A secondary analysis focusing on American participants enrolled in the Reduction of Cardiovascular Events with Icosapent Ethyl-Intervention Trial (REDUCE-IT) showed that these patients receive a similar benefit in terms of cardiovascular risk reduction with icosapent ethyl as compared with the entire trial population. A post hoc analysis of the Further Cardiovascular Outcomes Research with PCSK9 Inhibition in Subjects with Elevated Risk (FOURIER) trial demonstrated that a genetic risk score comprising 27 single-nucleotide polymorphisms is associated with cardiovascular risk among patients with established atherosclerotic CVD and patients with high genetic risk receive a relatively higher benefit from evolocumab use. Similar results were observed with alirocumab use in a post hoc analysis of the ODYSSEY OUTCOMES trial where a genome-wide polygenic risk score comprising 6.5 million DNA variants was used. These studies presented at 2019 AHA Scientific Sessions will help guide our approach to preventing CVD.
本次综述重点介绍了在 2019 年美国心脏协会(AHA)科学会议上提出的一些心血管疾病(CVD)预防研究。
在 2019 年 AHA 科学会议上提出了几项重要的心血管预防研究。秋水仙碱心血管结局试验(COLCOT)的结果表明,低剂量秋水仙碱可降低近期心肌梗死患者复发性心血管事件的风险。来自英国生物库队列的前瞻性分析表明,与不确定潜在克隆性造血相关的 CVD 风险增加可通过抑制促炎 IL-1β/IL-6 途径的 IL6R 基因常见破坏突变得到缓解。Treat Stroke to Target 试验表明,与 LDL-C 目标值为 90-110mg/dL 相比,降低缺血性卒中和短暂性脑缺血发作患者的低密度脂蛋白胆固醇至<70mg/dL,可降低复发性 CVD 事件的风险。一项针对美国参与者的二次分析,纳入了依泽替米贝降低心血管风险试验(REDUCE-IT),结果表明与整个试验人群相比,这些患者接受依折麦布治疗可获得相似的心血管风险降低获益。进一步心血管结局研究与 PCSK9 抑制剂在高危患者中的应用(FOURIER)试验的事后分析表明,包含 27 个单核苷酸多态性的遗传风险评分与已确诊动脉粥样硬化性 CVD 患者和高遗传风险患者的心血管风险相关,高遗传风险患者使用依洛尤单抗获益相对更高。在 ODYSSEY OUTCOMES 试验的事后分析中,也观察到了类似的结果,该试验使用了包含 650 万个 DNA 变体的全基因组多基因风险评分。这些在 2019 年 AHA 科学会议上提出的研究将有助于指导我们预防 CVD 的方法。