Right ventricular-pulmonary arterial coupling in schistosomiasis associated pulmonary arterial hypertension

IF 6 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Heart and Lung Transplantation Pub Date : 2025-07-01 Epub Date: 2025-02-11 DOI:10.1016/j.healun.2025.01.018
Jose Leonidas Alves-Jr , Eduardo Leite Vieira Costa , Susana Hoette , Caio Julio Cesar dos Santos Fernandes , Henrique Barbosa Ribeiro , Alexandre Antonio Cunha Abizaid , Marcela Araújo Castro , Bruna Mamprim Piloto , Pedro Alves Lemos , Carlos Viana Poyares Jardim , Ryan J. Tedford , Rogerio Souza
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Abstract

Background

Schistosomiasis associated pulmonary arterial hypertension (Sch-PAH) is a highly relevant form of pulmonary hypertension, particularly in developing countries. Compared with idiopathic pulmonary arterial hypertension (IPAH), Sch-PAH has a better prognosis, though without identified mechanisms that justify this clinical course. Right ventricular-arterial pulmonary (RV-PA) coupling, expressed by the relationship between right ventricular contractility and afterload, has been studied as a potential marker of cardiac response to pulmonary vascular disease. However, there are no studies evaluating RV-PA coupling in Sch-PAH.

Methods

Retrospective cohort including patients diagnosed with Sch-PAH or IPAH who underwent right heart catheterization (RHC) at our institution from 2013 to 2018. Clinical and hemodynamic characteristics were reviewed and, by means of the recorded and digitized RHC pressure curves, right ventricular maximum isovolumic pressure (Pmaxiso) was estimated through the single-beat method to calculate right ventricular elastance at the end systole (Ees). The RV-PA was expressed by the Ees and the pulmonary artery elastance (Ea) ratio.

Results

A total of 101 patients were included (33 with Sch-PAH and 68 with IPAH). Sch-PAH patients were older (55.5 ± 15.1 vs 42.7 ± 15.2; p <0.001) with no significant difference in terms of traditional hemodynamics; nevertheless, Sch-PAH patients had better survival (p=0.031). Patients with Sch-PAH showed higher RV-PA coupling (0.95±0,58 vs 0.67±0.41; p = 0.004), higher Ees (2.07±1.65 vs 1.33±0.91; p = 0.005) without any difference in Pmaxiso and Ea compared with IPAH. At univariate analysis, RV-PA coupling was associated with survival. The RV-PA coupling remained an independent prognostic marker in the multivariable analysis adjusted for the type of pulmonary arterial hypertension (p = 0.030; HR = 0.287; 95% CI, 0.093–0.883).

Conclusions

RV-PA coupling is better preserved in Sch-PAH patients and is significantly associated with survival, suggesting that the right ventricular response to the increased afterload in Sch-PAH might represent an important pathophysiological mechanism that could explain the better clinical course observed in this relevant form of PAH.
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血吸虫病相关肺动脉高压的右心室-肺动脉耦合。
背景:血吸虫病相关肺动脉高压(Sch-PAH)是一种高度相关的肺动脉高压形式,特别是在发展中国家。与特发性肺动脉高压(IPAH)相比,Sch-PAH有更好的预后,尽管没有确定的机制来证明这一临床过程。右心室-动脉-肺(RV-PA)偶联由右心室收缩力和后负荷之间的关系表达,已被研究作为心脏对肺血管疾病反应的潜在标志。然而,尚无研究评估Sch-PAH中RV-PA偶联。方法:回顾性队列研究纳入2013年至2018年在我院行右心导管(RHC)治疗的诊断为Sch-PAH或IPAH的患者。回顾临床和血流动力学特征,通过记录和数字化的RHC压力曲线,通过单拍法计算收缩期末右心室弹性,估计右心室最大等容压(Pmaxiso)。RV-PA由Ees和肺动脉弹性(Ea)比值表达。结果:共纳入101例患者,其中Sch-PAH 33例,IPAH 68例。Sch-PAH患者年龄较大(55.5±15.1 vs 42.7±15.2;结论:RV-PA偶联在Sch-PAH患者中得到更好的保存,并与生存率显著相关,这表明右心室对Sch-PAH后负荷增加的反应可能是一种重要的病理生理机制,可以解释在这种相关形式的PAH中观察到的更好的临床病程。
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来源期刊
CiteScore
10.10
自引率
6.70%
发文量
1667
审稿时长
69 days
期刊介绍: The Journal of Heart and Lung Transplantation, the official publication of the International Society for Heart and Lung Transplantation, brings readers essential scholarly and timely information in the field of cardio-pulmonary transplantation, mechanical and biological support of the failing heart, advanced lung disease (including pulmonary vascular disease) and cell replacement therapy. Importantly, the journal also serves as a medium of communication of pre-clinical sciences in all these rapidly expanding areas.
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