Recurrent severe preschool wheeze: From pre-specified diagnostic labels to underlying endotypes
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Published version
Author(s)
Type
Journal Article
Abstract
Rationale: Preschool wheezing is heterogeneous, but the underlying mechanisms are poorly understood. Objectives: To investigate lower airway inflammation and infection in preschool children with different clinical diagnoses undergoing elective bronchoscopy/bronchoalveolar lavage-BAL. Methods: We recruited 136 children aged 1-5 years (105 recurrent severe wheeze-RSW; 31 non-wheeze respiratory disorders-NWRD). RSW were assigned as episodic viral-EVW or multiple trigger wheeze-MTW. We compared lower airway inflammation/infection in different clinical diagnoses and undertook data-driven analyses to determine clusters of pathophysiological features, and investigated their relationships with pre-specified diagnostic labels. Measurements and Main Results: Blood eosinophils and allergic sensitization were significantly higher in RSW than NWRD. Blood neutrophils, BAL eosinophils and neutrophils, and positive bacterial culture and virus detection rates were similar between groups. However, pathogen distribution differed significantly, with higher detection of rhinovirus in RSW and Moraxella in sensitized RSW. EVW and MTW did not differ in blood/BAL inflammation, or bacterial/virus detection. Partition Around Medoids algorithm revealed 4 clusters of pathophysiological features: (1) Atopic (17.9%); (2) Non-atopic, low infection rate, high inhaled corticosteroids-ICS (31.3%); (3) Non-atopic, high infection rate (23.1%); and (4) Non-atopic, low infection rate, no ICS (27.6%). Cluster allocation differed significantly between RSW and NWRD (RSW evenly distributed across clusters, 60% of NWRD assigned to cluster 4, p<0.001). There was no difference in cluster membership between EVW and MTW. Cluster 1 was dominated by Moraxella detection (p=0.04) and Cluster 3 by Haemophilus/Staphylococcus/ Streptococcus (p=0.02). Conclusions: We identified four clusters of severe preschool wheeze distinguished using sensitization, peripheral eosinophilia, lower airway neutrophilia and bacteriology. This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/)
Date Issued
2021-05-07
Date Acceptance
2021-05-05
Citation
American Journal of Respiratory and Critical Care Medicine, 2021, 204 (5), pp.523-535
ISSN
1073-449X
Publisher
American Thoracic Society
Start Page
523
End Page
535
Journal / Book Title
American Journal of Respiratory and Critical Care Medicine
Volume
204
Issue
5
Copyright Statement
© 2021 by the American Thoracic Society. This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License 4.0.
Sponsor
British Lung Foundation
National Institute for Health Research
Identifier
https://www.atsjournals.org/doi/10.1164/rccm.202009-3696OC
Grant Number
RG14-12
CDF-2014-07-019
Subjects
Science & Technology
Life Sciences & Biomedicine
Critical Care Medicine
Respiratory System
General & Internal Medicine
pediatric wheeze
cluster analysis
infection
inflammation
endotypes
PERSISTENT ASTHMA
YOUNG-CHILDREN
INDUCED SPUTUM
INFLAMMATION
INFANTS
CONFIRMATION
ASSOCIATION
PHENOTYPES
LAVAGE
cluster analysis
endotypes
infection
inflammation
pediatric wheeze
Asthma
Child, Preschool
Female
Genetic Variation
Genotype
Humans
Infant
Male
Phenotype
Respiratory Sounds
Risk Factors
Severity of Illness Index
Symptom Assessment
Humans
Asthma
Respiratory Sounds
Severity of Illness Index
Risk Factors
Genotype
Phenotype
Child, Preschool
Infant
Female
Male
Genetic Variation
Symptom Assessment
Respiratory System
11 Medical and Health Sciences
Publication Status
Published
Date Publish Online
2021-05-07