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Characterisation of patients with severe asthma in the UK Severe Asthma Registry in the biologic era
BACKGROUND: The UK Severe Asthma Registry (UKSAR) is the world’s largest national severe asthma registry collecting standardised data on referrals to UK specialist services. Novel biologic therapies have transformed the management of type 2(T2)-high severe asthma but have highlighted unmet need in p...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7892381/ https://www.ncbi.nlm.nih.gov/pubmed/33298582 http://dx.doi.org/10.1136/thoraxjnl-2020-215168 |
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author | Jackson, David J Busby, John Pfeffer, Paul E Menzies-Gow, Andrew Brown, Thomas Gore, Robin Doherty, Martin Mansur, Adel H Message, Simon Niven, Robert Patel, Mitesh Heaney, Liam G |
author_facet | Jackson, David J Busby, John Pfeffer, Paul E Menzies-Gow, Andrew Brown, Thomas Gore, Robin Doherty, Martin Mansur, Adel H Message, Simon Niven, Robert Patel, Mitesh Heaney, Liam G |
author_sort | Jackson, David J |
collection | PubMed |
description | BACKGROUND: The UK Severe Asthma Registry (UKSAR) is the world’s largest national severe asthma registry collecting standardised data on referrals to UK specialist services. Novel biologic therapies have transformed the management of type 2(T2)-high severe asthma but have highlighted unmet need in patients with persisting symptoms despite suppression of T2-cytokine pathways with corticosteroids. METHODS: Demographic, clinical and treatments characteristics for patients meeting European Respiratory Society / American Thoracic Society severe asthma criteria were examined for 2225 patients attending 15 specialist severe asthma centres. We assessed differences in biomarker low patients (fractional exhaled nitric oxide (FeNO) <25 ppb, blood eosinophils <150/μL) compared with a biomarker high population (FeNO ≥25 ppb, blood eosinophils ≥150/µL). RESULTS: Age (mean 49.6 (14.3) y), age of asthma onset (24.2 (19.1) y) and female predominance (62.4%) were consistent with prior severe asthma cohorts. Poor symptom control (Asthma Control Questionnaire-6: 2.9 (1.4)) with high exacerbation rate (4 (IQR: 2, 7)) were common despite high-dose treatment (51.7% on maintenance oral corticosteroids (mOCS)). 68.9% were prescribed biologic therapies including mepolizumab (50.3%), benralizumab (26.1%) and omalizumab (22.6%). T2-low patients had higher body mass index (32.1 vs 30.2, p<0.001), depression/anxiety prevalence (12.3% vs 7.6%, p=0.04) and mOCS use (57.9% vs 42.1%, p<0.001). Many T2-low asthmatics had evidence of a historically elevated blood eosinophil count (0.35 (0.13, 0.60)). CONCLUSIONS: The UKSAR describes the characteristics of a large cohort of asthmatics referred to UK specialist severe asthma services. It offers the prospect of providing novel insights across a range of research areas and highlights substantial unmet need with poor asthma control, impaired lung function and high exacerbation rates. T2-high phenotypes predominate with significant differences apparent from T2-low patients. However, T2-low patients frequently have prior blood eosinophilia consistent with possible excessive corticosteroid exposure. |
format | Online Article Text |
id | pubmed-7892381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-78923812021-03-03 Characterisation of patients with severe asthma in the UK Severe Asthma Registry in the biologic era Jackson, David J Busby, John Pfeffer, Paul E Menzies-Gow, Andrew Brown, Thomas Gore, Robin Doherty, Martin Mansur, Adel H Message, Simon Niven, Robert Patel, Mitesh Heaney, Liam G Thorax Asthma BACKGROUND: The UK Severe Asthma Registry (UKSAR) is the world’s largest national severe asthma registry collecting standardised data on referrals to UK specialist services. Novel biologic therapies have transformed the management of type 2(T2)-high severe asthma but have highlighted unmet need in patients with persisting symptoms despite suppression of T2-cytokine pathways with corticosteroids. METHODS: Demographic, clinical and treatments characteristics for patients meeting European Respiratory Society / American Thoracic Society severe asthma criteria were examined for 2225 patients attending 15 specialist severe asthma centres. We assessed differences in biomarker low patients (fractional exhaled nitric oxide (FeNO) <25 ppb, blood eosinophils <150/μL) compared with a biomarker high population (FeNO ≥25 ppb, blood eosinophils ≥150/µL). RESULTS: Age (mean 49.6 (14.3) y), age of asthma onset (24.2 (19.1) y) and female predominance (62.4%) were consistent with prior severe asthma cohorts. Poor symptom control (Asthma Control Questionnaire-6: 2.9 (1.4)) with high exacerbation rate (4 (IQR: 2, 7)) were common despite high-dose treatment (51.7% on maintenance oral corticosteroids (mOCS)). 68.9% were prescribed biologic therapies including mepolizumab (50.3%), benralizumab (26.1%) and omalizumab (22.6%). T2-low patients had higher body mass index (32.1 vs 30.2, p<0.001), depression/anxiety prevalence (12.3% vs 7.6%, p=0.04) and mOCS use (57.9% vs 42.1%, p<0.001). Many T2-low asthmatics had evidence of a historically elevated blood eosinophil count (0.35 (0.13, 0.60)). CONCLUSIONS: The UKSAR describes the characteristics of a large cohort of asthmatics referred to UK specialist severe asthma services. It offers the prospect of providing novel insights across a range of research areas and highlights substantial unmet need with poor asthma control, impaired lung function and high exacerbation rates. T2-high phenotypes predominate with significant differences apparent from T2-low patients. However, T2-low patients frequently have prior blood eosinophilia consistent with possible excessive corticosteroid exposure. BMJ Publishing Group 2021-03 2020-12-09 /pmc/articles/PMC7892381/ /pubmed/33298582 http://dx.doi.org/10.1136/thoraxjnl-2020-215168 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Asthma Jackson, David J Busby, John Pfeffer, Paul E Menzies-Gow, Andrew Brown, Thomas Gore, Robin Doherty, Martin Mansur, Adel H Message, Simon Niven, Robert Patel, Mitesh Heaney, Liam G Characterisation of patients with severe asthma in the UK Severe Asthma Registry in the biologic era |
title | Characterisation of patients with severe asthma in the UK Severe Asthma Registry in the biologic era |
title_full | Characterisation of patients with severe asthma in the UK Severe Asthma Registry in the biologic era |
title_fullStr | Characterisation of patients with severe asthma in the UK Severe Asthma Registry in the biologic era |
title_full_unstemmed | Characterisation of patients with severe asthma in the UK Severe Asthma Registry in the biologic era |
title_short | Characterisation of patients with severe asthma in the UK Severe Asthma Registry in the biologic era |
title_sort | characterisation of patients with severe asthma in the uk severe asthma registry in the biologic era |
topic | Asthma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7892381/ https://www.ncbi.nlm.nih.gov/pubmed/33298582 http://dx.doi.org/10.1136/thoraxjnl-2020-215168 |
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