VCU Pauley Heart Center, Division of Cardiology, Department of Internal Medicine, Richmond, VA.
VCU Pauley Heart Center, Division of Cardiology, Department of Internal Medicine, Richmond, VA; Department of Kinesiology and Health Sciences, Virginia Commonwealth University, Richmond, VA.
Am J Cardiol. 2018 Oct 15;122(8):1366-1370. doi: 10.1016/j.amjcard.2018.07.002. Epub 2018 Jul 20.
Interleukin-1β (IL-1β) is a cytokine involved in atherothrombosis and is known to depress cardiac function. We hypothesized that blocking IL-1β in patients with symptomatic systolic heart failure (HF) would improve their cardiorespiratory fitness. The purpose of the study was to measure changes in peak oxygen consumption (VO) in 30 patients with prior myocardial infarction, high-sensitivity C-reactive protein ≥ 2 mg/l and HF with left ventricular ejection fraction (LVEF) < 50% enrolled in the Canakinumab Anti-inflammatory Thrombosis Outcome Study (CANTOS) in an independent single center substudy. We measured peak VO before and after 3 and 12 months of treatment with Canakinumab every 3 months (50, 150, or 300mg subcutaneously) or placebo, and measured LVEF before and after 12 months. In December 2013, the CANTOS study announced early termination of enrollment, halting enrollment for this substudy after only 15 patients, of which 3 were assigned to placebo and 12 to Canakinumab (50mg [1; 7%], 150mg [5; 33%], 300mg [6; 40%]). Patients treated with Canakinumab had a significant improvement in peak VO, from 19.2 to 22.8 ml/kg/min at 3 months (p = 0.023 within-group changes, p = 0.026 for time_x_group interaction versus placebo [primary end point]), and an improvement in LVEF 38% (33-43) to 44% (38-52) at 12 months (p = 0.012 for within-group changes). No significant changes were seen in the placebo group. In conclusion, the findings of this small prespecified secondary analysis of the CANTOS trial support the positive results of the overall study, and confirm IL-1 as a potential therapeutic target in HF. https://clinicaltrials.gov/ct2/show/NCT01900600.
白细胞介素-1β(IL-1β)是一种参与动脉血栓形成的细胞因子,已知其可抑制心脏功能。我们假设,在有症状的收缩性心力衰竭(HF)患者中阻断 IL-1β 可改善其心肺适应性。本研究的目的是在独立的单中心亚研究中,测量 30 例先前有心肌梗死、高敏 C 反应蛋白≥2mg/L 和左心室射血分数(LVEF)<50%的 HF 患者在接受依那西普抗炎血栓结局研究(CANTOS)治疗 3 个月和 12 个月后,峰值摄氧量(VO)的变化。我们每 3 个月测量一次患者接受 Canakinumab(皮下注射 50、150 或 300mg)或安慰剂治疗前和治疗后 3 个月和 12 个月的峰值 VO,并在治疗 12 个月后测量 LVEF。2013 年 12 月,CANTOS 研究宣布提前终止入组,该亚研究仅在 15 例患者后停止入组,其中 3 例接受安慰剂,12 例接受 Canakinumab(50mg[1;7%]、150mg[5;33%]、300mg[6;40%])。接受 Canakinumab 治疗的患者的峰值 VO 显著提高,从治疗 3 个月时的 19.2 增加到 22.8ml/kg/min(组内变化,p=0.023;与安慰剂相比,时间×组交互作用,p=0.026),在 12 个月时 LVEF 从 38%(33-43)增加到 44%(38-52)(组内变化,p=0.012)。安慰剂组无明显变化。总之,这项对 CANTOS 试验的小预设二次分析的结果支持了总体研究的积极结果,并证实了白细胞介素-1 作为 HF 的潜在治疗靶点。https://clinicaltrials.gov/ct2/show/NCT01900600。