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Upper-Airway Microbiome, Mucociliary Function, and Clinical Outcomes in Bronchiectasis: Data from the EMBARC-BRIDGE
Hayoung Choi1, Hollian Richardson2, Chandani Hennayake2
1Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Internal Medicine, Hallym University Kangnam Sacred Heart Hospital, Seoul, Republic of Korea.
The upper-airway microbiome composition in bronchiectasis patients is linked to disease severity and exacerbations. Nasopharyngeal dysbiosis, particularly with Pseudomonas, correlates with worse clinical outcomes and more severe respiratory symptoms.
Area of Science:
- Microbiology
- Pulmonology
- Genetics
Background:
- Infections significantly drive disease progression in bronchiectasis.
- The upper-airway microbiome influences the lower-airway microbiome composition.
- Understanding this relationship is crucial for managing bronchiectasis.
Purpose of the Study:
- To investigate the association between the upper-airway microbiome, mucociliary function, and clinical outcomes in bronchiectasis patients.
- To identify specific microbial patterns linked to disease severity and exacerbations.
- To assess the stability of the upper-airway microbiome over time.
Main Methods:
- Collected nasopharyngeal swabs from 344 bronchiectasis patients across five European centers.
- Analyzed microbiome composition, α-diversity (Chao1), and β-diversity (Bray-Curtis).
- Utilized random forest analysis and defined dysbiosis based on pathogenic taxa abundance (Pseudomonas, Haemophilus, Staphylococcus).
Main Results:
- α-Diversity significantly differed by disease severity (P=0.002).
- Distinct microbiome profiles were associated with disease severity and severe exacerbations (P=0.021 and P=0.001, respectively).
- Pseudomonas abundance correlated with severe bronchiectasis, exacerbations, and sputum Pseudomonas aeruginosa growth; dysbiosis linked to worse symptoms and outcomes.
Conclusions:
- The upper-airway microbiome composition is significantly associated with bronchiectasis severity.
- Nasopharyngeal dysbiosis is a predictor of more severe clinical outcomes and exacerbations.
- Microbiome profiles demonstrated relative stability between baseline and 1-year follow-up.
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