Van Tassell Benjamin W, Lipinski Michael J, Appleton Darryn, Roberts Charlotte S, Kontos Michael C, Abouzaki Nayef, Melchior Ryan, Mueller George, Garnett James, Canada Justin, Carbone Salvatore, Buckley Leo F, Wohlford George, Kadariya Dinesh, Trankle Cory R, Oddi Erdle Claudia, Sculthorpe Robin, Puckett Laura, DeWilde Christine, Shah Keyur, Angiolillo Dominick J, Vetrovec George, Biondi-Zoccai Giuseppe, Arena Ross, Abbate Antonio
VCU Pauley Heart Center, Virginia Commonwealth University, Richmond, Virginia.
Department of Pharmacotherapy and Outcomes Science, Virginia Commonwealth University, Richmond, Virginia.
Clin Cardiol. 2018 Aug;41(8):1004-1008. doi: 10.1002/clc.22988. Epub 2018 Aug 17.
There is clear association between the intensity of the acute inflammatory response during acute myocardial infarction (AMI) and adverse prognosis after AMI. Interleukin-1 (IL-1) is a pro-inflammatory cytokine released during AMI and involved in adverse remodeling and heart failure (HF). We describe a study to evaluate the safety and efficacy of IL-1 blockade using an IL-1 receptor antagonist (anakinra) during the acute phase of ST-segment elevation myocardial infarction (STEMI). The Virginia Commonwealth University-Anakinra Remodeling Trial-3 (VCU-ART3; http://www.ClinicalTrials.gov NCT01950299) is a phase 2, multicenter, double-blinded, randomized, placebo-controlled clinical trial comparing anakinra 100 mg once or twice daily vs matching placebo (1:1:1) for 14 days in 99 patients with STEMI. Patients who present to the hospital with STEMI within 12 hours of symptom onset will be eligible for enrollment. Patients will be excluded for a history of HF (functional class III-IV), severe valvular disease, severe kidney disease (stage 4-5), active infection, recent use of immunosuppressive drugs, active malignancy, or chronic autoimmune/auto-inflammatory diseases. We will measure the difference in the area under the curve for C-reactive protein between admission and day 14, separately comparing each of the anakinra groups with the placebo group. The P value will be considered significant if <0.025 to adjust for multiple comparisons. Patients will also be followed for up to 12 months from enrollment to evaluate cardiac remodeling (echocardiography), cardiac function (echocardiography), and major adverse cardiovascular outcomes (cardiovascular death, MI, revascularization, and new onset of HF).
急性心肌梗死(AMI)期间急性炎症反应的强度与AMI后的不良预后之间存在明确关联。白细胞介素-1(IL-1)是AMI期间释放的一种促炎细胞因子,参与不良重塑和心力衰竭(HF)。我们描述了一项研究,旨在评估在ST段抬高型心肌梗死(STEMI)急性期使用IL-1受体拮抗剂(阿那白滞素)阻断IL-1的安全性和有效性。弗吉尼亚联邦大学-阿那白滞素重塑试验-3(VCU-ART3;http://www.ClinicalTrials.gov NCT01950299)是一项2期、多中心、双盲、随机、安慰剂对照临床试验,在99例STEMI患者中比较每日1次或2次100 mg阿那白滞素与匹配安慰剂(1:1:1),疗程为14天。症状发作后12小时内入院的STEMI患者符合入组条件。有HF病史(功能分级III-IV级)、严重瓣膜病、严重肾病(4-5期)、活动性感染、近期使用免疫抑制药物、活动性恶性肿瘤或慢性自身免疫/自身炎症性疾病的患者将被排除。我们将测量入院时和第14天时C反应蛋白曲线下面积的差异,分别将每个阿那白滞素组与安慰剂组进行比较。为校正多重比较,若P值<0.025则认为具有显著性。从入组开始,还将对患者进行长达12个月的随访,以评估心脏重塑(超声心动图)、心功能(超声心动图)和主要不良心血管事件(心血管死亡、心肌梗死、血运重建和HF新发)。