Interleukin-1 Blockade in Patients With ST-Segment Elevation Myocardial Infarction Across the Spectrum of Coronary Artery Disease Complexity.

IF 2.6 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Martin Denicolai, Matteo Morello, Michele Golino, Giuliana Corna, Marco G Del Buono, Carla R Agatiello, Benjamin W Van Tassell, Antonio Abbate
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引用次数: 0

Abstract

Patients with ST-segment elevation myocardial infarction (STEMI) and complex coronary artery disease (CAD) face a poor prognosis, including increased heart failure (HF) risk. Phase 2 clinical trials of anakinra have shown inhibition of the acute inflammatory response and prevention of HF after STEMI, but data on its effects based on CAD complexity are lacking. We performed a pooled secondary analysis of 139 patients with STEMI. The SYNTAX (Synergy Between Percutaneous Coronary Intervention with Taxus and Cardiac Surgery), SYNTAX II and Gensini scores were calculated, and patients were divided into two groups below and above the median. We evaluated the effect of anakinra on the area-under-the-curve of high-sensitivity C-reactive protein (hsCRP-AUC) at 14 days, and the composite endpoint of new-onset HF, HF hospitalization, or all-cause death at 1-year follow-up using Kaplan-Meier survival curves, Cox regression analysis for Hazard Ratios (HR), and tested interactions between subgroups. All three CAD complexity scores (SYNTAX, SYNTAX II and Gensini) were associated with an increased risk of adverse events (HR 1.02 to 1.06, all p-values ≤0.025). We found no statistically significant interactions between CAD extent, measured as single-vessel or multi-vessel CAD, SYNTAX score ≤9 or >9, SYNTAX II score ≤24 or >24, Gensini score ≤32 or >32, and treatment effect of anakinra on hsCRP-AUC or the composite clinical endpoint (all p-values for interaction >0.05). In conclusion, among patients with STEMI, IL-1 blockade with anakinra significantly attenuated the acute inflammatory response and reduced the risk of HF-related events regardless of the spectrum of CAD complexity.

白细胞介素-1阻断剂在ST段抬高型心肌梗死患者中的应用跨越了冠状动脉疾病复杂性的范围。
ST段抬高型心肌梗死(STEMI)和复杂冠状动脉疾病(CAD)患者预后不良,包括心力衰竭(HF)风险增加。anakinra的2期临床试验显示,它能抑制急性炎症反应并预防STEMI后的心力衰竭,但缺乏基于CAD复杂性的效果数据。我们对 139 名 STEMI 患者进行了汇总二次分析。我们计算了 SYNTAX(Taxus 经皮冠状动脉介入治疗与心脏手术之间的协同作用)、SYNTAX II 和 Gensini 评分,并将患者分为低于和高于中位数的两组。我们使用 Kaplan-Meier 生存曲线、危险比 (HR) 的 Cox 回归分析评估了 Anakinra 对 14 天时高敏 C 反应蛋白曲线下面积 (hsCRP-AUC) 以及随访 1 年时新发 HF、HF 住院或全因死亡复合终点的影响,并测试了亚组之间的交互作用。所有三种 CAD 复杂性评分(SYNTAX、SYNTAX II 和 Gensini)均与不良事件风险增加有关(HR 1.02 至 1.06,所有 p 值均≤0.025)。我们发现,单血管或多血管CAD、SYNTAX评分≤9分或>9分、SYNTAX II评分≤24分或>24分、Gensini评分≤32分或>32分等CAD程度与anakinra对hsCRP-AUC或复合临床终点的治疗效果之间没有统计学意义上的交互作用(所有交互作用的p值均>0.05)。总之,在 STEMI 患者中,无论 CAD 的复杂程度如何,使用 anakinra 阻断 IL-1 都能显著减轻急性炎症反应并降低 HF 相关事件的风险。
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
367
审稿时长
1 months
期刊介绍: Journal of Cardiovascular Pharmacology is a peer reviewed, multidisciplinary journal that publishes original articles and pertinent review articles on basic and clinical aspects of cardiovascular pharmacology. The Journal encourages submission in all aspects of cardiovascular pharmacology/medicine including, but not limited to: stroke, kidney disease, lipid disorders, diabetes, systemic and pulmonary hypertension, cancer angiogenesis, neural and hormonal control of the circulation, sepsis, neurodegenerative diseases with a vascular component, cardiac and vascular remodeling, heart failure, angina, anticoagulants/antiplatelet agents, drugs/agents that affect vascular smooth muscle, and arrhythmias. Appropriate subjects include new drug development and evaluation, physiological and pharmacological bases of drug action, metabolism, drug interactions and side effects, application of drugs to gain novel insights into physiology or pathological conditions, clinical results with new and established agents, and novel methods. The focus is on pharmacology in its broadest applications, incorporating not only traditional approaches, but new approaches to the development of pharmacological agents and the prevention and treatment of cardiovascular diseases. Please note that JCVP does not publish work based on biological extracts of mixed and uncertain chemical composition or unknown concentration.
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