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Pathophysiological characterization of asthma transitions across adolescence
BACKGROUND: Adolescence is a period of change, which coincides with disease remission in a significant proportion of subjects with childhood asthma. There is incomplete understanding of the changing characteristics underlying different adolescent asthma transitions. We undertook pathophysiological c...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256730/ https://www.ncbi.nlm.nih.gov/pubmed/25472820 http://dx.doi.org/10.1186/s12931-014-0153-7 |
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author | Arshad, Syed Hasan Raza, Abid Lau, Laurie Bawakid, Khalid Karmaus, Wilfried Zhang, Hongmei Ewart, Susan Patil, Veersh Roberts, Graham Kurukulaaratchy, Ramesh |
author_facet | Arshad, Syed Hasan Raza, Abid Lau, Laurie Bawakid, Khalid Karmaus, Wilfried Zhang, Hongmei Ewart, Susan Patil, Veersh Roberts, Graham Kurukulaaratchy, Ramesh |
author_sort | Arshad, Syed Hasan |
collection | PubMed |
description | BACKGROUND: Adolescence is a period of change, which coincides with disease remission in a significant proportion of subjects with childhood asthma. There is incomplete understanding of the changing characteristics underlying different adolescent asthma transitions. We undertook pathophysiological characterization of transitional adolescent asthma phenotypes in a longitudinal birth cohort. METHODS: The Isle of Wight Birth Cohort (N = 1456) was reviewed at 1, 2, 4, 10 and 18-years. Characterization included questionnaires, skin tests, spirometry, exhaled nitric oxide, bronchial challenge and (in a subset of 100 at 18-years) induced sputum. Asthma groups were “never asthma” (no asthma since birth), “persistent asthma” (asthma at age 10 and 18), “remission asthma” (asthma at age 10 but not at 18) and “adolescent-onset asthma” (asthma at age 18 but not at age 10). RESULTS: Participants whose asthma remitted during adolescence had lower bronchial reactivity (odds ratio (OR) 0.30; CI 0.10 -0.90; p = 0.03) at age 10 plus greater improvement in lung function (forced expiratory flow 25-75% gain: 1.7 L; 1.0-2.9; p = 0.04) compared to persistent asthma by age 18. Male sex (0.3; 0.1-0.7; p < 0.01) and lower acetaminophen use (0.4; 0.2-0.8; p < 0.01) independently favoured asthma remission, when compared to persistent asthma. Asthma remission had a lower total sputum cell count compared to never asthma (31.5 [25–75 centiles] 12.9-40.4) vs. 47.0 (19.5-181.3); p = 0.03). Sputum examination in adolescent-onset asthma showed eosinophilic airway inflammation (3.0%, 0.7-6.6), not seen in persistent asthma (1.0%, 0–3.9), while remission group had the lowest sputum eosinophil count (0.3%, 0–1.4) and lowest eosinophils/neutrophils ratio of 0.0 (Interquartile range: 0.1). CONCLUSION: Asthma remission during adolescence is associated with lower initial BHR and greater gain in small airways function, while adolescent-onset asthma is primarily eosinophilic. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-014-0153-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4256730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42567302014-12-05 Pathophysiological characterization of asthma transitions across adolescence Arshad, Syed Hasan Raza, Abid Lau, Laurie Bawakid, Khalid Karmaus, Wilfried Zhang, Hongmei Ewart, Susan Patil, Veersh Roberts, Graham Kurukulaaratchy, Ramesh Respir Res Research BACKGROUND: Adolescence is a period of change, which coincides with disease remission in a significant proportion of subjects with childhood asthma. There is incomplete understanding of the changing characteristics underlying different adolescent asthma transitions. We undertook pathophysiological characterization of transitional adolescent asthma phenotypes in a longitudinal birth cohort. METHODS: The Isle of Wight Birth Cohort (N = 1456) was reviewed at 1, 2, 4, 10 and 18-years. Characterization included questionnaires, skin tests, spirometry, exhaled nitric oxide, bronchial challenge and (in a subset of 100 at 18-years) induced sputum. Asthma groups were “never asthma” (no asthma since birth), “persistent asthma” (asthma at age 10 and 18), “remission asthma” (asthma at age 10 but not at 18) and “adolescent-onset asthma” (asthma at age 18 but not at age 10). RESULTS: Participants whose asthma remitted during adolescence had lower bronchial reactivity (odds ratio (OR) 0.30; CI 0.10 -0.90; p = 0.03) at age 10 plus greater improvement in lung function (forced expiratory flow 25-75% gain: 1.7 L; 1.0-2.9; p = 0.04) compared to persistent asthma by age 18. Male sex (0.3; 0.1-0.7; p < 0.01) and lower acetaminophen use (0.4; 0.2-0.8; p < 0.01) independently favoured asthma remission, when compared to persistent asthma. Asthma remission had a lower total sputum cell count compared to never asthma (31.5 [25–75 centiles] 12.9-40.4) vs. 47.0 (19.5-181.3); p = 0.03). Sputum examination in adolescent-onset asthma showed eosinophilic airway inflammation (3.0%, 0.7-6.6), not seen in persistent asthma (1.0%, 0–3.9), while remission group had the lowest sputum eosinophil count (0.3%, 0–1.4) and lowest eosinophils/neutrophils ratio of 0.0 (Interquartile range: 0.1). CONCLUSION: Asthma remission during adolescence is associated with lower initial BHR and greater gain in small airways function, while adolescent-onset asthma is primarily eosinophilic. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-014-0153-7) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-29 2014 /pmc/articles/PMC4256730/ /pubmed/25472820 http://dx.doi.org/10.1186/s12931-014-0153-7 Text en © Arshad et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Arshad, Syed Hasan Raza, Abid Lau, Laurie Bawakid, Khalid Karmaus, Wilfried Zhang, Hongmei Ewart, Susan Patil, Veersh Roberts, Graham Kurukulaaratchy, Ramesh Pathophysiological characterization of asthma transitions across adolescence |
title | Pathophysiological characterization of asthma transitions across adolescence |
title_full | Pathophysiological characterization of asthma transitions across adolescence |
title_fullStr | Pathophysiological characterization of asthma transitions across adolescence |
title_full_unstemmed | Pathophysiological characterization of asthma transitions across adolescence |
title_short | Pathophysiological characterization of asthma transitions across adolescence |
title_sort | pathophysiological characterization of asthma transitions across adolescence |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256730/ https://www.ncbi.nlm.nih.gov/pubmed/25472820 http://dx.doi.org/10.1186/s12931-014-0153-7 |
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