Pulmonary hypertension associated with COPD: a phenotype analysis.

IF 4.4 3区 医学 Q1 RESPIRATORY SYSTEM ERJ Open Research Pub Date : 2025-03-24 eCollection Date: 2025-03-01 DOI:10.1183/23120541.00716-2024
Mathilde Steger, Matthieu Canuet, Guillaume Martin, Aissam Labani, Jean Charles Schwartz, Irina Enache, Armelle Schuller, Léo Meyer, Ari Chaouat, Romain Kessler, David Montani, Marianne Riou
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Abstract

Background: Pulmonary hypertension (PH) associated with COPD (PH-COPD) exhibits diverse phenotypes, challenging therapeutic management. This study aimed to describe the characteristics of COPD patients with distinct phenotypes, namely end-stage COPD with or without PH (group 1), other COPD patients with mild-to-moderate pre-capillary PH-COPD (group 2) and COPD patients with a pulmonary vascular phenotype (PVP) (group 3).

Methods: We performed a retrospective analysis of COPD patients who underwent right heart catheterisation from 2015 to 2022.

Results: 81 patients were included in group 1, 37 in group 2 and 35 in group 3. The groups differed in terms of clinical, functional, haemodynamic and imaging characteristics. Group 1 had significantly marked lung hyperinflation with increased total lung capacity and residual volume, a feature not observed in group 3. These results were confirmed by analysis of chest CT scans, which confirmed varying degrees of emphysema, as follows: severe in group 1, moderate in group 2 and mild in group 3, with median total emphysema indices of 55% (48-62), 32% (16-49) and 16% (3.4-31), respectively, p<0.0001.

Conclusions: Our results highlight the broad spectrum of PH in COPD, from PH associated with end-stage COPD (phenotype/group 1), characterised by predominant alveolar wall damage with severe emphysema, to PVP (phenotype/group 3), mainly due to pulmonary vascular changes. Phenotype/group 2 represents an intermediate state combining features of both. In the current debate on how to distinguish PH-COPD phenotypes, it might be of interest to include quantitative thresholds for emphysema in future diagnostic and management algorithms.

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肺动脉高压与COPD相关:一项表型分析
背景:肺动脉高压(PH)与慢性阻塞性肺病(PH-COPD)表现出多种表型,具有挑战性的治疗管理。本研究旨在描述具有不同表型的COPD患者的特征,即伴或不伴PH的终末期COPD(1组),其他轻度至中度毛细血管前PH-COPD(2组)和伴肺血管表型(PVP)的COPD患者(3组)。方法:我们对2015年至2022年接受右心导管置入的COPD患者进行回顾性分析。结果:1组81例,2组37例,3组35例。两组在临床、功能、血流动力学和影像学特征上存在差异。第1组有明显的肺恶性膨胀,肺总容量和残余容量增加,而第3组没有观察到这一特征。通过对胸部CT扫描结果的分析,证实了这些结果,证实了不同程度的肺气肿,1组为重度,2组为中度,3组为轻度,总肺气肿指数中位数分别为55%(48-62),32%(16-49)和16%(3.4-31)。我们的研究结果强调了COPD中PH的广谱性,从PH与终末期COPD(表型/组1)相关,特征是主要肺泡壁损伤伴严重肺气肿,到PVP(表型/组3),主要是由于肺血管改变。表型/组2代表一种结合两者特征的中间状态。在目前关于如何区分PH-COPD表型的争论中,在未来的诊断和管理算法中纳入肺气肿的定量阈值可能会引起人们的兴趣。
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来源期刊
ERJ Open Research
ERJ Open Research Medicine-Pulmonary and Respiratory Medicine
CiteScore
6.20
自引率
4.30%
发文量
273
审稿时长
8 weeks
期刊介绍: ERJ Open Research is a fully open access original research journal, published online by the European Respiratory Society. The journal aims to publish high-quality work in all fields of respiratory science and medicine, covering basic science, clinical translational science and clinical medicine. The journal was created to help fulfil the ERS objective to disseminate scientific and educational material to its members and to the medical community, but also to provide researchers with an affordable open access specialty journal in which to publish their work.
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