Leary Peter J, Rayner Samuel G, Branch Kelley R H, Hogl Laurie, Liston Nancy M, Barros Lia M, Prout Jessi, Nolley Stephanie, Buber Jonathan, Ralph David D, Probstfield Jeffrey L
Division of Pulmonary, Critical Care, and Sleep Medicine, University of Washington, Seattle, WA; Department of Epidemiology, University of Washington, Seattle, WA.
Division of Pulmonary, Critical Care, and Sleep Medicine, University of Washington, Seattle, WA.
Chest. 2025 Jul;168(1):189-199. doi: 10.1016/j.chest.2024.12.029. Epub 2025 Jan 4.
Adaptation of the right ventricle is a key determinant of outcomes in pulmonary arterial hypertension (PAH). Despite a compelling rationale to develop targeted therapies for the right ventricle in PAH, no such treatments exist. H-receptor antagonism is a potential myocardial-focused paradigm in heart failure.
Do H-receptor antagonists improve outcomes in patients with PAH?
We conducted a 24-week, single-center, 1:1 randomized, double-masked, placebo-controlled trial of the H-receptor antagonist famotidine in patients with a diagnosis of PAH. The primary outcome was change in 6-minute walk distance (6MWD) at 24 weeks. Secondary end points included B-type natriuretic peptide levels, New York Heart Association functional class, right ventricular parameters measured from echocardiography, health-related quality of life, and escalation in PAH-focused care.
From May 2019 through July 2023, 80 participants were randomized with 79 receiving study drug. No significant difference in the primary outcome of 6MWD at 24 weeks was found, with an increase of 4.7 m seen in the placebo arm vs a decrease of 17.0 m in the famotidine arm (P = .24). Also no differences were found in secondary end points at 24 weeks. Study drug was well tolerated, and safety profiles were similar between arms. Adherence and study conduct were good overall. Participants with methamphetamine-associated PAH were similar in all aspects to the study participants more broadly.
The results of this trial do not support the routine use of famotidine 20 mg daily as an adjunct therapy for the treatment of PAH. The findings of the Repurposing a Histamine Antagonist to Benefit Patients With Pulmonary Hypertension (REHAB-PH) trial argue against the practice of avoiding participants with methamphetamine-associated PAH in randomized clinical trials of novel therapies.
ClinicalTrials.gov; No.: NCT03554291; URL: www.
gov.
右心室适应性是肺动脉高压(PAH)预后的关键决定因素。尽管有充分的理由开发针对PAH右心室的靶向治疗方法,但目前尚无此类治疗方法。H受体拮抗作用是心力衰竭中一种潜在的以心肌为重点的范例。
H受体拮抗剂能否改善PAH患者的预后?
我们对诊断为PAH的患者进行了一项为期24周、单中心、1:1随机、双盲、安慰剂对照试验,使用H受体拮抗剂法莫替丁。主要结局是24周时6分钟步行距离(6MWD)的变化。次要终点包括B型利钠肽水平、纽约心脏协会功能分级、超声心动图测量的右心室参数、健康相关生活质量以及PAH重点护理的升级情况。
从2019年5月到2023年7月,80名参与者被随机分组,79人接受研究药物治疗。24周时6MWD的主要结局未发现显著差异,安慰剂组增加了4.7米,而法莫替丁组减少了17.0米(P = 0.24)。24周时次要终点也未发现差异。研究药物耐受性良好,两组的安全性概况相似。总体而言,依从性和研究开展情况良好。与甲基苯丙胺相关的PAH患者在各方面与更广泛的研究参与者相似。
该试验结果不支持每日常规使用20毫克法莫替丁作为PAH治疗的辅助疗法。组胺拮抗剂用于肺动脉高压患者(REHAB-PH)试验的结果反对在新型疗法的随机临床试验中避开与甲基苯丙胺相关的PAH患者的做法。
ClinicalTrials.gov;编号:NCT03554291;网址:www.clinicaltrials.gov 。