Mitrovic Veselin, Seferovic Petar M, Simeunovic Dejan, Ristic Arsen D, Miric Milutin, Moiseyev Valentin S, Kobalava Zhanna, Nitsche Klaus, Forssmann Wolf-Georg, Lüss Hartmut, Meyer Markus
Kerckhoff-Klinik, Bad Nauheim, Germany.
Eur Heart J. 2006 Dec;27(23):2823-32. doi: 10.1093/eurheartj/ehl337. Epub 2006 Oct 30.
Ularitide is a synthetic form of urodilatin, a natriuretic peptide produced in the kidney with vasodilating, natriuretic, and diuretic effects, that offers promise for the management of decompensated heart failure (DHF). We assessed the efficacy and safety of ularitide in treating patients with DHF.
In this Phase II randomized, double-blind, placebo-controlled trial, 221 DHF patients received either placebo (n=53) or ularitide at 7.5 ng/kg/min (n=60), 15 ng/kg/min (n=53), or 30 ng/kg/min (n=55) as a 24-h continuous infusion. At 6 h, ularitide demonstrated a significant decrease in pulmonary capillary wedge pressure (P=0.052, P=0.000004, P=0.000002, respectively) and improved dyspnoea score in the 7.5, 15, and 30 ng/kg/min ularitide group (P=0.0026, P=0.0026, P=0.0013, respectively). Ularitide reduced systemic vascular resistance and increased cardiac index for the 15 and 30 ng/kg/min groups (P=0.017, P=0.00002, respectively). Systolic blood pressure (BP) decreased dose dependency. Heart rate and serum creatinine were unchanged through day 3. Most frequently reported drug-related adverse events through day 3 in all ularitide groups were dose-dependent BP decrease and hypotension.
Ularitide lowered cardiac filling pressures and improved dyspnoea without apparent early deleterious effects on renal function in DHF patients. These results suggest that ularitide may play a role in the management of DHF.
ularitide是尿舒张素的一种合成形式,尿舒张素是一种在肾脏中产生的利钠肽,具有血管舒张、利钠和利尿作用,有望用于治疗失代偿性心力衰竭(DHF)。我们评估了ularitide治疗DHF患者的疗效和安全性。
在这项II期随机、双盲、安慰剂对照试验中,221例DHF患者接受安慰剂(n = 53)或ularitide,分别以7.5 ng/kg/分钟(n = 60)、15 ng/kg/分钟(n = 53)或30 ng/kg/分钟(n = 55)的剂量进行24小时持续输注。在6小时时,ularitide在7.5、15和30 ng/kg/分钟的ularitide组中分别使肺毛细血管楔压显著降低(P分别为0.052、0.000004、0.000002),并改善了呼吸困难评分(P分别为0.0026、0.0026、0.0013)。在15和30 ng/kg/分钟的组中,ularitide降低了全身血管阻力并增加了心脏指数(P分别为0.017、0.00002)。收缩压(BP)呈剂量依赖性下降。至第3天,心率和血清肌酐未发生变化。在所有ularitide组中,至第3天最常报告的与药物相关的不良事件是剂量依赖性血压下降和低血压。
Ularitide可降低DHF患者的心脏充盈压并改善呼吸困难,且对肾功能无明显早期有害影响。这些结果表明ularitide可能在DHF的治疗中发挥作用。