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Revisiting Late-Onset Asthma: Clinical Characteristics and Association with Allergy
The Global Initiative for Asthma (GINA) 2020 defines late-onset asthma (LOA) as one of the clinical phenotypes of asthma wherein patients, particularly women, present with asthma for the first time in adult life, tend to be non-allergic and often require higher doses of inhaled corticosteroids (ICS)...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781019/ https://www.ncbi.nlm.nih.gov/pubmed/33408487 http://dx.doi.org/10.2147/JAA.S282205 |
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author | Quirce, Santiago Heffler, Enrico Nenasheva, Natalia Demoly, Pascal Menzies-Gow, Andrew Moreira-Jorge, Ana Nissen, Francis Hanania, Nicola A |
author_facet | Quirce, Santiago Heffler, Enrico Nenasheva, Natalia Demoly, Pascal Menzies-Gow, Andrew Moreira-Jorge, Ana Nissen, Francis Hanania, Nicola A |
author_sort | Quirce, Santiago |
collection | PubMed |
description | The Global Initiative for Asthma (GINA) 2020 defines late-onset asthma (LOA) as one of the clinical phenotypes of asthma wherein patients, particularly women, present with asthma for the first time in adult life, tend to be non-allergic and often require higher doses of inhaled corticosteroids (ICS) or are relatively refractory to corticosteroid treatment. In this review, we examine the published literature improve the understanding of the following aspects of LOA: 1) the age cut-off for its diagnosis; 2) its distinct clinical phenotypes, characteristics and risk factors; and 3) its association with allergic comorbidities and conditions. Overall, our review reveals that clinicians and researchers have used multiple age cut-offs to define LOA, with cut-off ages ranging from >12 years to ≥65 years. LOA has also been classified into several distinct phenotypes, some of which drastically differ in their clinical characteristics, course and prognosis. Although LOA has traditionally been considered non-allergic in nature, our review indicates that it is commonly associated with allergic features and comorbidities. Our findings suggest that there is an urgent need for the development of more clear clinical practice guidelines that can provide more clarity on the definition and other aspects of LOA. In addition, the association of LOA and allergy needs to be re-examined to frame a more optimal treatment strategy for patients with LOA. |
format | Online Article Text |
id | pubmed-7781019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-77810192021-01-05 Revisiting Late-Onset Asthma: Clinical Characteristics and Association with Allergy Quirce, Santiago Heffler, Enrico Nenasheva, Natalia Demoly, Pascal Menzies-Gow, Andrew Moreira-Jorge, Ana Nissen, Francis Hanania, Nicola A J Asthma Allergy Review The Global Initiative for Asthma (GINA) 2020 defines late-onset asthma (LOA) as one of the clinical phenotypes of asthma wherein patients, particularly women, present with asthma for the first time in adult life, tend to be non-allergic and often require higher doses of inhaled corticosteroids (ICS) or are relatively refractory to corticosteroid treatment. In this review, we examine the published literature improve the understanding of the following aspects of LOA: 1) the age cut-off for its diagnosis; 2) its distinct clinical phenotypes, characteristics and risk factors; and 3) its association with allergic comorbidities and conditions. Overall, our review reveals that clinicians and researchers have used multiple age cut-offs to define LOA, with cut-off ages ranging from >12 years to ≥65 years. LOA has also been classified into several distinct phenotypes, some of which drastically differ in their clinical characteristics, course and prognosis. Although LOA has traditionally been considered non-allergic in nature, our review indicates that it is commonly associated with allergic features and comorbidities. Our findings suggest that there is an urgent need for the development of more clear clinical practice guidelines that can provide more clarity on the definition and other aspects of LOA. In addition, the association of LOA and allergy needs to be re-examined to frame a more optimal treatment strategy for patients with LOA. Dove 2020-12-31 /pmc/articles/PMC7781019/ /pubmed/33408487 http://dx.doi.org/10.2147/JAA.S282205 Text en © 2020 Quirce et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Quirce, Santiago Heffler, Enrico Nenasheva, Natalia Demoly, Pascal Menzies-Gow, Andrew Moreira-Jorge, Ana Nissen, Francis Hanania, Nicola A Revisiting Late-Onset Asthma: Clinical Characteristics and Association with Allergy |
title | Revisiting Late-Onset Asthma: Clinical Characteristics and Association with Allergy |
title_full | Revisiting Late-Onset Asthma: Clinical Characteristics and Association with Allergy |
title_fullStr | Revisiting Late-Onset Asthma: Clinical Characteristics and Association with Allergy |
title_full_unstemmed | Revisiting Late-Onset Asthma: Clinical Characteristics and Association with Allergy |
title_short | Revisiting Late-Onset Asthma: Clinical Characteristics and Association with Allergy |
title_sort | revisiting late-onset asthma: clinical characteristics and association with allergy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781019/ https://www.ncbi.nlm.nih.gov/pubmed/33408487 http://dx.doi.org/10.2147/JAA.S282205 |
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