Severe pulmonary hypertension associated with lung disease is characterised by a loss of small pulmonary vessels on quantitative computed tomography.


Journal

ERJ open research
ISSN: 2312-0541
Titre abrégé: ERJ Open Res
Pays: England
ID NLM: 101671641

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 13 08 2021
accepted: 10 02 2022
entrez: 19 5 2022
pubmed: 20 5 2022
medline: 20 5 2022
Statut: epublish

Résumé

Pulmonary hypertension (PH) in patients with chronic lung disease (CLD) predicts reduced functional status, clinical worsening and increased mortality, with patients with severe PH-CLD (≥35 mmHg) having a significantly worse prognosis than mild to moderate PH-CLD (21-34 mmHg). The aim of this cross-sectional study was to assess the association between computed tomography (CT)-derived quantitative pulmonary vessel volume, PH severity and disease aetiology in CLD. Treatment-naïve patients with CLD who underwent CT pulmonary angiography, lung function testing and right heart catheterisation were identified from the ASPIRE registry between October 2012 and July 2018. Quantitative assessments of total pulmonary vessel and small pulmonary vessel volume were performed. 90 patients had PH-CLD including 44 associated with COPD/emphysema and 46 with interstitial lung disease (ILD). Patients with severe PH-CLD (n=40) had lower small pulmonary vessel volume compared to patients with mild to moderate PH-CLD (n=50). Patients with PH-ILD had significantly reduced small pulmonary blood vessel volume, compared to PH-COPD/emphysema. Higher mortality was identified in patients with lower small pulmonary vessel volume. Patients with severe PH-CLD, regardless of aetiology, have lower small pulmonary vessel volume compared to patients with mild-moderate PH-CLD, and this is associated with a higher mortality. Whether pulmonary vessel changes quantified by CT are a marker of remodelling of the distal pulmonary vasculature requires further study.

Sections du résumé

Background UNASSIGNED
Pulmonary hypertension (PH) in patients with chronic lung disease (CLD) predicts reduced functional status, clinical worsening and increased mortality, with patients with severe PH-CLD (≥35 mmHg) having a significantly worse prognosis than mild to moderate PH-CLD (21-34 mmHg). The aim of this cross-sectional study was to assess the association between computed tomography (CT)-derived quantitative pulmonary vessel volume, PH severity and disease aetiology in CLD.
Methods UNASSIGNED
Treatment-naïve patients with CLD who underwent CT pulmonary angiography, lung function testing and right heart catheterisation were identified from the ASPIRE registry between October 2012 and July 2018. Quantitative assessments of total pulmonary vessel and small pulmonary vessel volume were performed.
Results UNASSIGNED
90 patients had PH-CLD including 44 associated with COPD/emphysema and 46 with interstitial lung disease (ILD). Patients with severe PH-CLD (n=40) had lower small pulmonary vessel volume compared to patients with mild to moderate PH-CLD (n=50). Patients with PH-ILD had significantly reduced small pulmonary blood vessel volume, compared to PH-COPD/emphysema. Higher mortality was identified in patients with lower small pulmonary vessel volume.
Conclusion UNASSIGNED
Patients with severe PH-CLD, regardless of aetiology, have lower small pulmonary vessel volume compared to patients with mild-moderate PH-CLD, and this is associated with a higher mortality. Whether pulmonary vessel changes quantified by CT are a marker of remodelling of the distal pulmonary vasculature requires further study.

Identifiants

pubmed: 35586449
doi: 10.1183/23120541.00503-2021
pii: 00503-2021
pmc: PMC9108962
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Wellcome Trust
ID : 205188/Z/16/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M008894/1
Pays : United Kingdom
Organisme : British Heart Foundation
ID : SP/14/6/31350
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206632/Z/17/Z
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/18/13/33281
Pays : United Kingdom

Informations de copyright

Copyright ©The authors 2022.

Déclaration de conflit d'intérêts

Conflict of interest: D. Alkhanfar has nothing to disclose. Conflict of interest: Y. Shahin has nothing to disclose. Conflict of interest: F. Alandejani has nothing to disclose. Conflict of interest: K. Dwivedi has nothing to disclose. Conflict of interest: S. Alabed has nothing to disclose. Conflict of interest: C. Johns has nothing to disclose. Conflict of interest: A. Lawrie has nothing to disclose. Conflict of interest: A.A.R. Thompson has nothing to disclose. Conflict of interest: A.M.K. Rothman has nothing to disclose. Conflict of interest: J. Tschirren has nothing to disclose. Conflict of interest: J.M. Uthoff has nothing to disclose. Conflict of interest: E. Hoffman has nothing to disclose. Conflict of interest: R. Condliffe has nothing to disclose. Conflict of interest: J.M. Wild has nothing to disclose. Conflict of interest: D.G. Kiely has nothing to disclose. Conflict of interest: A.J. Swift has nothing to disclose.

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Auteurs

Dheyaa Alkhanfar (D)

Dept of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
INSIGNEO, Institute for In Silico Medicine, University of Sheffield, Sheffield, UK.

Yousef Shahin (Y)

Dept of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
Dept of Clinical Radiology, Sheffield Teaching Hospitals, Sheffield, UK.

Faisal Alandejani (F)

Dept of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.

Krit Dwivedi (K)

Dept of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.

Samer Alabed (S)

Dept of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
Dept of Clinical Radiology, Sheffield Teaching Hospitals, Sheffield, UK.

Chris Johns (C)

Dept of Clinical Radiology, Sheffield Teaching Hospitals, Sheffield, UK.

Allan Lawrie (A)

Dept of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.

A A Roger Thompson (AAR)

Dept of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
Sheffield Pulmonary Vascular Disease Unit, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Alexander M K Rothman (AMK)

Dept of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
Sheffield Pulmonary Vascular Disease Unit, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Juerg Tschirren (J)

VIDA Diagnostics Inc., Coralville, IA, USA.

Johanna M Uthoff (JM)

Dept of Computer Science, University of Sheffield, Sheffield, UK.

Eric Hoffman (E)

Dept of Radiology, University of Iowa, Iowa City, IA, USA.

Robin Condliffe (R)

Sheffield Pulmonary Vascular Disease Unit, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Jim M Wild (JM)

Dept of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
INSIGNEO, Institute for In Silico Medicine, University of Sheffield, Sheffield, UK.

David G Kiely (DG)

INSIGNEO, Institute for In Silico Medicine, University of Sheffield, Sheffield, UK.
Sheffield Pulmonary Vascular Disease Unit, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
These authors contributed equally.

Andrew J Swift (AJ)

Dept of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
INSIGNEO, Institute for In Silico Medicine, University of Sheffield, Sheffield, UK.
These authors contributed equally.

Classifications MeSH