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静脉给予重组人神经调节蛋白-1 可使稳定的慢性心力衰竭患者产生有利的急性和慢性血液动力学反应。

Parenteral administration of recombinant human neuregulin-1 to patients with stable chronic heart failure produces favourable acute and chronic haemodynamic responses.

机构信息

Cardiology Department, St Vincent's Hospital, Darlinghurst, 2010 NSW, Australia.

出版信息

Eur J Heart Fail. 2011 Jan;13(1):83-92. doi: 10.1093/eurjhf/hfq152. Epub 2010 Sep 1.

Abstract

AIMS

Neuregulin-1 (NRG-1) plays a critical role in the adaptation of the heart to injury, inhibiting apoptosis and inducing cardiomyocyte proliferation. We have shown previously that rhNRG-1 improves cardiac function and survival in animal models of cardiomyopathy. Here we report the first human study aimed at exploring the acute and chronic haemodynamic responses to recombinant human NRG-1 (beta(2a) isoform; rhNRG-1) in patients with stable chronic heart failure (CHF).

METHODS AND RESULTS

Fifteen patients (age, 60 ± 2; NYHA II:III, 9:6; left ventricular ejection fraction (LVEF) <40%) on optimal medical therapy for CHF, received a rhNRG-1 infusion daily for 11 days. Acute and chronic haemodynamic, structural and biochemical effects were determined by serial right heart catheterization, cardiac magnetic resonance (CMR), echocardiography and measurement of neurohumoral indices. Acutely, cardiac output increased by 30% during a 6 h rhNRG-1 infusion (P < 0.01). Pulmonary artery wedge pressure and systemic vascular resistance decreased 30 and 20%, respectively, at 2 h (P < 0.01). A 47% reduction in serum noradrenaline, a 55% reduction in serum aldosterone and a 3.6-fold increase in N-terminal prohormone brain natriuretic peptide levels were concurrently observed (P < 0.001). These acute haemodynamic effects were sustained, as demonstrated by the 12% increase in LVEF from 32.2 ± 2.0% (baseline) to 36.1 ± 2.3% (mean ± SE, P < 0.001) at 12 weeks. The therapy was well tolerated.

CONCLUSION

rhNRG-1 appears to produce favourable acute and chronic haemodynamic effects in patients with stable CHF on optimal medical therapy. Randomized controlled trials of rhNRG-1 in cardiac disease are thus warranted. Clinical Trial Registration Information The trial was registered with the Australian New Zealand Clinical Trials Registry, anzctr.org.au Identifier: ACTRN12607000330448.

摘要

目的

神经调节蛋白-1(NRG-1)在心脏适应损伤方面起着关键作用,可抑制细胞凋亡并诱导心肌细胞增殖。我们之前已经表明,rhNRG-1 可改善心肌病动物模型的心脏功能和存活率。在这里,我们报告了首例旨在探索重组人 NRG-1(β(2a)异构体;rhNRG-1)在稳定型慢性心力衰竭(CHF)患者中的急性和慢性血液动力学反应的人体研究。

方法和结果

15 名患者(年龄 60±2;NYHA II:III 为 9:6;左心室射血分数(LVEF)<40%)接受了最佳的 CHF 药物治疗,每天接受 rhNRG-1 输注 11 天。通过连续右心导管检查、心脏磁共振(CMR)、超声心动图和神经激素指数的测量来确定急性和慢性血液动力学、结构和生化效应。在 6 小时 rhNRG-1 输注期间,心输出量增加了 30%(P<0.01)。肺动脉楔压和全身血管阻力分别在 2 小时时降低了 30%和 20%(P<0.01)。同时观察到血清去甲肾上腺素降低 47%、血清醛固酮降低 55%和 N 端脑钠肽前体水平升高 3.6 倍(P<0.001)。这些急性血液动力学效应是持续的,12 周时 LVEF 从 32.2±2.0%(基线)增加到 36.1±2.3%(平均值±SE,P<0.001),证明了这一点。该治疗耐受良好。

结论

rhNRG-1 似乎在接受最佳药物治疗的稳定型 CHF 患者中产生有利的急性和慢性血液动力学效应。因此,有必要进行 rhNRG-1 在心脏病中的随机对照试验。

临床试验注册信息

该试验在澳大利亚和新西兰临床试验注册中心注册,anzctr.org.au 标识符:ACTRN12607000330448。

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