Evidence map›Paper›PMID 40129550›Full record

ArticleERJ open research2025

Pulmonary hypertension associated with COPD: a phenotype analysis.

Mathilde Steger, Matthieu Canuet, Guillaume Martin, Aissam Labani, Jean Charles Schwartz, Irina Enache, Armelle Schuller, Léo Meyer, Ari Chaouat, Romain Kessler and 2 more

Abstract read
In one paragraph

Article in ERJ open research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Mathilde StegerChest Diseases Department, Nouvel hôpital civil, University Hospital of Strasbourg, Strasbourg, France.ORCID https://orcid.org/0009-0003-4260-2042
Matthieu CanuetChest Diseases Department, Nouvel hôpital civil, University Hospital of Strasbourg, Strasbourg, France.ORCID https://orcid.org/0000-0002-8089-4846
Guillaume MartinChest Diseases Department, Nouvel hôpital civil, University Hospital of Strasbourg, Strasbourg, France.
Aissam LabaniRadiology Department, Nouvel hôpital civil, University Hospital of Strasbourg, Strasbourg, France.
Jean Charles SchwartzRadiology Department, Nouvel hôpital civil, University Hospital of Strasbourg, Strasbourg, France.ORCID https://orcid.org/0000-0002-8637-4593
Irina EnacheDepartment of Physiology and Functional Exploration, Nouvel hôpital civil, University Hospital of Strasbourg, Strasbourg, France.
Armelle SchullerChest Diseases Department, Nouvel hôpital civil, University Hospital of Strasbourg, Strasbourg, France.
Léo MeyerRadiology Department, Nouvel hôpital civil, University Hospital of Strasbourg, Strasbourg, France.
Ari ChaouatChest Diseases Department - Medical Specialties Division, CHRU, Nancy, France.ORCID https://orcid.org/0000-0001-6056-202X
Romain KesslerChest Diseases Department, Nouvel hôpital civil, University Hospital of Strasbourg, Strasbourg, France.
David MontaniUniversity of Paris-Saclay, AP-HP, Chest diseases department, Hospital of Bicêtre, DMU 5 Thorinno, Inserm UMR_S999, Le Kremlin Bicêtre, France.ORCID https://orcid.org/0000-0002-9358-6922
Marianne RiouChest Diseases Department, Nouvel hôpital civil, University Hospital of Strasbourg, Strasbourg, France.ORCID https://orcid.org/0000-0001-6807-8582

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Identifiers

PMID40129550
PMCPMC11931555

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