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Sputum microbiome profiles identify severe asthma phenotypes of relative stability at 12 to 18 months

Authors :
John H. Riley
Peter H. Howarth
Anke H. Maitland-van der Zee
Sven-Erik Dahlén
Kian Fan Chung
Anne H. Neerincx
Peter J. Sterk
Mahmoud I. Abdel-Aziz
Nazanin Zounemat Kermani
Ian M. Adcock
Susanne J. H. Vijverberg
Paul Brinkman
Stewart Bates
Simone Hashimoto
Ratko Djukanovic
Aletta D. Kraneveld
Pharmacology
Afd Pharmacology
Pharmacoepidemiology and Clinical Pharmacology
Commission of the European Communities
Pulmonology
Graduate School
APH - Personalized Medicine
AII - Inflammatory diseases
AII - Cancer immunology
Paediatric Pulmonology
ARD - Amsterdam Reproduction and Development
Source :
Journal of Allergy and Clinical Immunology, 147(1), 123. Mosby Inc., Journal of allergy and clinical immunology, 147(1), 123-134. Mosby Inc.
Publication Year :
2021

Abstract

Background: Asthma is a heterogeneous disease characterized by distinct phenotypes with associated microbial dysbiosis. Objectives: Our aim was to identify severe asthma phenotypes based on sputum microbiome profiles and assess their stability after 12 to 18 months. A further aim was to evaluate clusters’ robustness after inclusion of an independent cohort of patients with mild-to-moderate asthma. Methods: In this longitudinal multicenter cohort study, sputum samples were collected for microbiome profiling from a subset of the Unbiased Biomarkers in Prediction of Respiratory Disease Outcomes adult patient cohort at baseline and after 12 to 18 months of follow-up. Unsupervised hierarchical clustering was performed by using the Bray-Curtis β-diversity measure of microbial profiles. For internal validation, partitioning around medoids, consensus cluster distribution, bootstrapping, and topological data analysis were applied. Follow-up samples were studied to evaluate within-patient clustering stability in patients with severe asthma. Cluster robustness was evaluated by using an independent cohort of patients with mild-to-moderate asthma. Results: Data were available for 100 subjects with severe asthma (median age 55 years; 42% males). Two microbiome-driven clusters were identified; they were characterized by differences in asthma onset, smoking status, residential locations, percentage of blood and/or sputum neutrophils and macrophages, lung spirometry results, and concurrent asthma medications (all P values < .05). The cluster 2 patients displayed a commensal-deficient bacterial profile that was associated with worse asthma outcomes than those of the cluster 1 patients. Longitudinal clusters revealed high relative stability after 12 to 18 months in those with severe asthma. Further inclusion of an independent cohort of 24 patients with mild-to-moderate asthma was consistent with the clustering assignments. Conclusion: Unbiased microbiome-driven clustering revealed 2 distinct robust phenotypes of severe asthma that exhibited relative overtime stability. This suggests that the sputum microbiome may serve as a biomarker for better characterizing asthma phenotypes.

Details

Language :
English
ISSN :
00916749
Database :
OpenAIRE
Journal :
Journal of Allergy and Clinical Immunology, 147(1), 123. Mosby Inc., Journal of allergy and clinical immunology, 147(1), 123-134. Mosby Inc.
Accession number :
edsair.doi.dedup.....589156fca2532178264942d62ac5fc16