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Published on: January 21, 2018
The association between chronic rhinosinusitis, bronchiectasis and type 2 inflammation: an EMBARC registry analysis
Michal Shteinberg1,2, Charles S Haworth3, Jennifer Pollock4
1Pulmonology Institute, Carmel Medical Center, Haifa, Israel.
Chronic rhinosinusitis (CRS) is common in bronchiectasis, worsening symptoms. Type 2 inflammation markers link to CRS, but this connection depends on bronchiectasis cause, not appearing in primary ciliary dyskinesia or immune deficiency.
Area of Science:
- Pulmonology
- Immunology
- Otolaryngology
Background:
- Chronic rhinosinusitis (CRS) is a frequent comorbidity in bronchiectasis.
- Previous research linked CRS in bronchiectasis to elevated type 2 biomarkers, suggesting an
Purpose of the Study:
- To investigate CRS prevalence (with and without nasal polyposis) in bronchiectasis.
- To assess CRS impact on bronchiectasis outcomes.
- To explore the association between CRS and type 2 inflammatory biomarkers across different bronchiectasis etiologies.
Main Methods:
- Utilized data from the EMBARC bronchiectasis registry.
- Classified patients into no CRS, CRS without nasal polyposis (CRSnNP), or CRS with nasal polyposis (CRSwNP).
- Employed regression models to analyze CRS effects on symptoms and outcomes, and multivariate models for type 2 biomarkers (blood eosinophil count, total IgE).
Main Results:
- Identified CRS in 20.9% (CRSnNP) and 7.3% (CRSwNP) of 16,640 bronchiectasis patients.
- CRSwNP and CRSnNP correlated with worse symptoms and more exacerbations, but fewer hospitalizations and lower mortality.
- Elevated type 2 biomarkers were observed with CRSwNP in idiopathic bronchiectasis, but not in primary ciliary dyskinesia (PCD) or immune deficiency-related bronchiectasis.
Conclusions:
- CRS and nasal polyposis are significant comorbidities in bronchiectasis, linked to increased symptom burden and exacerbations.
- The association between elevated type 2 biomarkers and CRS in bronchiectasis is dependent on the underlying etiology.
- CRSwNP was independently associated with elevated type 2 biomarkers in multivariable analysis.
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