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Inorganic Nitrite Delivery to Improve Exercise Capacity in Heart Failure with Preserved Ejection Fraction (INDIE-HFpEF): Rationale and Design

机译:保留保留射血分数(INDIE-HFpEF)的无机亚硝酸盐传递以改善心力衰竭的运动能力:原理和设计

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摘要

Approximately half of patients with heart failure (HF) have preserved ejection fraction (HFpEF). There is no proven treatment that improves outcome. The pathophysiology of HFpEF is complex and includes left ventricular (LV) systolic and diastolic dysfunction, pulmonary vascular disease, endothelial dysfunction, and peripheral abnormalities. Multiple lines of evidence point to impaired nitric oxide-cyclic guanosine monophosphate (NO-cGMP) bioavailability as playing a central role in each of these abnormalities. In contrast to traditional organic nitrate therapies, an alternative strategy to restore NO-cGMP signaling is via inorganic nitrite. Inorganic nitrite, previously considered to be an inert byproduct of NO metabolism, functions as an important in vivo reservoir for NO generation, particularly under hypoxic and acidemic conditions. As such, inorganic nitrite becomes most active at times of greater need for NO signaling, as during exercise when LV filling pressures and pulmonary artery pressures increase. Herein, we present the rationale and design for the Inorganic Nitrite Delivery to Improve Exercise Capacity in Heart Failure with Preserved Ejection Fraction (INDIE-HFpEF) trial, which is a multicenter, randomized, double-blind, placebo controlled crossover study assessing the effect of inhaled inorganic nitrite on peak exercise capacity, conducted in the NHLBI-sponsored Heart Failure Clinical Research Network.>Clinical Trial Registration: clinicaltrials.gov;
机译:大约一半的心力衰竭(HF)患者保留射血分数(HFpEF)。没有有效的治疗方法可以改善预后。 HFpEF的病理生理很复杂,包括左心室(LV)收缩和舒张功能障碍,肺血管疾病,内皮功能障碍和周围异常。多种证据表明,一氧化氮-环鸟嘌呤单磷酸鸟苷(NO-cGMP)的生物利用度受损在这些异常中均起着核心作用。与传统的有机硝酸盐疗法相反,恢复NO-cGMP信号传导的替代策略是通过无机亚硝酸盐。以前被认为是NO代谢的惰性副产物的无机亚硝酸盐,在NO生成时,尤其是在低氧和强酸条件下,起着重要的体内NO生成的作用。因此,无机亚硝酸盐在需要大量NO信号时变得最活跃,例如在运动过程中,LV充盈压和肺动脉压升高。在此,我们介绍了通过保留射血分数(INDIE-HFpEF)试验来改善心力衰竭的运动能力的无机亚硝酸盐递送的原理和设计,该试验是一项多中心,随机,双盲,安慰剂对照的交叉研究,评估了>临床试验注册:clinicaltrials.gov;在NHLBI赞助的心力衰竭临床研究网络中进行了研究。

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