Asthma and fixed airflow obstruction: Long-term trajectories suggest distinct endotypes.


Journal

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology
ISSN: 1365-2222
Titre abrégé: Clin Exp Allergy
Pays: England
ID NLM: 8906443

Informations de publication

Date de publication:
01 2021
Historique:
received: 17 10 2019
revised: 18 03 2020
accepted: 29 05 2020
pubmed: 25 7 2020
medline: 15 1 2022
entrez: 25 7 2020
Statut: ppublish

Résumé

Long-term trajectories of asthma with fixed airflow obstruction (FAO) may reveal links to inflammatory endotypes. We investigated whether measures of asthma control and airway inflammation and remodelling differed by long-term FAO status in moderate-to-severe asthma. Adults enrolled in the Difficult Asthma Study assessed initially using serial Asthma Control Questionnaire (ACQ), exacerbation history, spirometry and sputum cytology over 12 months, as well as endoscopic bronchial biopsy with airway smooth muscle (ASM) quantification, were revaluated three or more years later with questionnaires and spirometry. FAO was defined as a persistent post-bronchodilator forced expired volume in one second (FEV Sixty-two participants (mean ± SD age 48 ± 11 years; 50% female; 75% atopic; asthma duration 24 ± 14 years) returned for follow-up assessment (median interval 7.9 years; IQR: 5.4-8.8 years). Compared to participants without FAO (n = 28), those with FAO at baseline and long-term follow-up (n = 18) had higher baseline sputum neutrophil content and ASM, and a higher exacerbation frequency that persisted at long-term follow-up. Sputum eosinophils, ACQ and long-term FEV In moderate-to-severe asthma, long-term FAO is characterized by neutrophilic sputum inflammation and airway remodelling, but FEV

Sections du résumé

BACKGROUND
Long-term trajectories of asthma with fixed airflow obstruction (FAO) may reveal links to inflammatory endotypes.
OBJECTIVE
We investigated whether measures of asthma control and airway inflammation and remodelling differed by long-term FAO status in moderate-to-severe asthma.
METHODS
Adults enrolled in the Difficult Asthma Study assessed initially using serial Asthma Control Questionnaire (ACQ), exacerbation history, spirometry and sputum cytology over 12 months, as well as endoscopic bronchial biopsy with airway smooth muscle (ASM) quantification, were revaluated three or more years later with questionnaires and spirometry. FAO was defined as a persistent post-bronchodilator forced expired volume in one second (FEV
RESULTS
Sixty-two participants (mean ± SD age 48 ± 11 years; 50% female; 75% atopic; asthma duration 24 ± 14 years) returned for follow-up assessment (median interval 7.9 years; IQR: 5.4-8.8 years). Compared to participants without FAO (n = 28), those with FAO at baseline and long-term follow-up (n = 18) had higher baseline sputum neutrophil content and ASM, and a higher exacerbation frequency that persisted at long-term follow-up. Sputum eosinophils, ACQ and long-term FEV
CONCLUSION
In moderate-to-severe asthma, long-term FAO is characterized by neutrophilic sputum inflammation and airway remodelling, but FEV

Identifiants

pubmed: 32706916
doi: 10.1111/cea.13714
doi:

Substances chimiques

Bronchodilator Agents 0
Glucocorticoids 0
Leukotriene Antagonists 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

39-48

Informations de copyright

© 2020 John Wiley & Sons Ltd.

Références

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Auteurs

Benjamin M Smith (BM)

McGill University Health Centre Research Institute, Montreal, QC, Canada.
Meakins-Christie Laboratories of McGill University, Montreal, QC, Canada.

Nan Zhao (N)

McGill University Health Centre Research Institute, Montreal, QC, Canada.

Ronald Olivenstein (R)

McGill University Health Centre Research Institute, Montreal, QC, Canada.
Meakins-Christie Laboratories of McGill University, Montreal, QC, Canada.

Catherine Lemiere (C)

Service de Pneumologie, Hôpital du Sacré-Coeur de Montréal, Université de Montréal, Montreal, QC, Canada.

Qutayba Hamid (Q)

McGill University Health Centre Research Institute, Montreal, QC, Canada.
Meakins-Christie Laboratories of McGill University, Montreal, QC, Canada.
University of Sharjah, Sharjah, United Arab Emirates.

James G Martin (JG)

McGill University Health Centre Research Institute, Montreal, QC, Canada.
Meakins-Christie Laboratories of McGill University, Montreal, QC, Canada.

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