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CFTR heterozygosity in severe asthma with recurrent airway infections: a retrospective review
RATIONALE: Patients with asthma who have neutrophilic bronchitis may have an underlying cause leading to increased susceptibility to airway infections. METHODS: Retrospective review of patients with asthma who had a previous history of recurrent exacerbations that had been associated with airway or...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172019/ https://www.ncbi.nlm.nih.gov/pubmed/35668512 http://dx.doi.org/10.1186/s13223-022-00684-0 |
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author | Priel, Eldar Adatia, Adil Kjarsgaard, Melanie Nair, Parameswaran |
author_facet | Priel, Eldar Adatia, Adil Kjarsgaard, Melanie Nair, Parameswaran |
author_sort | Priel, Eldar |
collection | PubMed |
description | RATIONALE: Patients with asthma who have neutrophilic bronchitis may have an underlying cause leading to increased susceptibility to airway infections. METHODS: Retrospective review of patients with asthma who had a previous history of recurrent exacerbations that had been associated with airway or sinus infections referred to a tertiary asthma center between 2005 and 2020. Demographics, clinical features, and airway inflammation type determined by sputum cytometry were compared between CFTR carriers and non-carriers. Multiple linear regression was used to identify clinical predictors of CFTR carrier status. Response to nebulized hypertonic saline was assessed by comparing the number of infective exacerbations before and after its initiation. RESULTS: 75 patients underwent CFTR mutation testing. Of these, 13 (17%) were CFTR carriers. The most common mutation was [Formula: see text] F508. CFTR carriers were older (adjusted odds ratio 1.06 (CI 95% 1.01, 1.13)) and had more frequent flares requiring hospitalization (4.19 (1.34, 24.74)). Neutrophilic airway inflammation was the most common inflammatory subtype in CFTR carriers, though 8/13 also had eosinophilic bronchitis. Nebulized hypertonic saline was well tolerated by most and reduced the frequency of infective exacerbations. CONCLUSIONS: The prevalence of CFTR heterozygosity in this cohort with recurrent neutrophilic bronchitis is higher than in the general population. Respiratory disease in CFTR carriers is associated with older age and may cause significant morbidity. Airway neutrophilia is the most common inflammatory subtype, but > 50% had eosinophilic bronchitis requiring treatment. Hypertonic saline appears to be well tolerated and effective in reducing the number of infective exacerbations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13223-022-00684-0. |
format | Online Article Text |
id | pubmed-9172019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91720192022-06-08 CFTR heterozygosity in severe asthma with recurrent airway infections: a retrospective review Priel, Eldar Adatia, Adil Kjarsgaard, Melanie Nair, Parameswaran Allergy Asthma Clin Immunol Research RATIONALE: Patients with asthma who have neutrophilic bronchitis may have an underlying cause leading to increased susceptibility to airway infections. METHODS: Retrospective review of patients with asthma who had a previous history of recurrent exacerbations that had been associated with airway or sinus infections referred to a tertiary asthma center between 2005 and 2020. Demographics, clinical features, and airway inflammation type determined by sputum cytometry were compared between CFTR carriers and non-carriers. Multiple linear regression was used to identify clinical predictors of CFTR carrier status. Response to nebulized hypertonic saline was assessed by comparing the number of infective exacerbations before and after its initiation. RESULTS: 75 patients underwent CFTR mutation testing. Of these, 13 (17%) were CFTR carriers. The most common mutation was [Formula: see text] F508. CFTR carriers were older (adjusted odds ratio 1.06 (CI 95% 1.01, 1.13)) and had more frequent flares requiring hospitalization (4.19 (1.34, 24.74)). Neutrophilic airway inflammation was the most common inflammatory subtype in CFTR carriers, though 8/13 also had eosinophilic bronchitis. Nebulized hypertonic saline was well tolerated by most and reduced the frequency of infective exacerbations. CONCLUSIONS: The prevalence of CFTR heterozygosity in this cohort with recurrent neutrophilic bronchitis is higher than in the general population. Respiratory disease in CFTR carriers is associated with older age and may cause significant morbidity. Airway neutrophilia is the most common inflammatory subtype, but > 50% had eosinophilic bronchitis requiring treatment. Hypertonic saline appears to be well tolerated and effective in reducing the number of infective exacerbations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13223-022-00684-0. BioMed Central 2022-06-06 /pmc/articles/PMC9172019/ /pubmed/35668512 http://dx.doi.org/10.1186/s13223-022-00684-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Priel, Eldar Adatia, Adil Kjarsgaard, Melanie Nair, Parameswaran CFTR heterozygosity in severe asthma with recurrent airway infections: a retrospective review |
title | CFTR heterozygosity in severe asthma with recurrent airway infections: a retrospective review |
title_full | CFTR heterozygosity in severe asthma with recurrent airway infections: a retrospective review |
title_fullStr | CFTR heterozygosity in severe asthma with recurrent airway infections: a retrospective review |
title_full_unstemmed | CFTR heterozygosity in severe asthma with recurrent airway infections: a retrospective review |
title_short | CFTR heterozygosity in severe asthma with recurrent airway infections: a retrospective review |
title_sort | cftr heterozygosity in severe asthma with recurrent airway infections: a retrospective review |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172019/ https://www.ncbi.nlm.nih.gov/pubmed/35668512 http://dx.doi.org/10.1186/s13223-022-00684-0 |
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