Low-dose budesonide/formoterol counteracts airway inflammation and improves lung function in COPD
File(s)Hakim et al AJRCCM 2018.pdf (104.5 KB)
Accepted version
Author(s)
Type
Journal Article
Abstract
The latest Global Initiative for Chronic Obstructive Lung Disease (GOLD) document recommends new treatment algorithms, with inhaled corticosteroids (ICS) use only in moderate-to-severely symptomatic COPD patients with repeated exacerbations, where
the emphasis is to review ICS use and to reduce ICS dosing (1). Indeed, safety concerns of pneumonia (2) with high-dose ICS has further concerted focus upon using appropriate doses of ICS. It is well-established that ICS in combination with long-acting β2-adrenoceptor agonist (LABA) can decrease exacerbations, improve symptoms
and increase quality of life in patients with COPD (3-4), but nonetheless, the rationale to consider step-down of ICS is supported by several clinical studies (5). The Withdrawal of Inhaled Steroids during Optimized Bronchodilator Management (WISDOM) trial studied
severe COPD patients on therapy with ICS, LAMA and LABA, where stepwise withdrawal of ICS did not lead to an increase in exacerbations compared to continued ICS use (6). Determining the optimal dose of ICS and LABA combination therapy is of great biological and clinical importance in order to address safety concerns associated with high-dose ICS use. There is in vitro
evidence to support the clinical practice of using low-dose ICS. Low-dose ICS in combination with LABA enhances corticosteroid function by enhancing glucocorticoid receptor (GR) activity (7) and suppresses the release of inflammatory mediators (8). However, it is unknown whether this observation of enhanced corticosteroid function with low-dose ICS/LABA has a direct effect on airways inflammation and lung function. Our study investigated the cellular function that may be
relevant and underpin the clinical approach to lowering the dose of ICS therapy in COPD patients. We compared the single administration of low-dose ICS/LABA combination to high-dose ICS alone and high-dose ICS/LABA on GR activation, molecular markers of AJRCCM as
airway inflammation and lung function in COPD patients 2 hours post-treatment. Some of the results of these studies have been previously reported in the form of an abstract (9).
the emphasis is to review ICS use and to reduce ICS dosing (1). Indeed, safety concerns of pneumonia (2) with high-dose ICS has further concerted focus upon using appropriate doses of ICS. It is well-established that ICS in combination with long-acting β2-adrenoceptor agonist (LABA) can decrease exacerbations, improve symptoms
and increase quality of life in patients with COPD (3-4), but nonetheless, the rationale to consider step-down of ICS is supported by several clinical studies (5). The Withdrawal of Inhaled Steroids during Optimized Bronchodilator Management (WISDOM) trial studied
severe COPD patients on therapy with ICS, LAMA and LABA, where stepwise withdrawal of ICS did not lead to an increase in exacerbations compared to continued ICS use (6). Determining the optimal dose of ICS and LABA combination therapy is of great biological and clinical importance in order to address safety concerns associated with high-dose ICS use. There is in vitro
evidence to support the clinical practice of using low-dose ICS. Low-dose ICS in combination with LABA enhances corticosteroid function by enhancing glucocorticoid receptor (GR) activity (7) and suppresses the release of inflammatory mediators (8). However, it is unknown whether this observation of enhanced corticosteroid function with low-dose ICS/LABA has a direct effect on airways inflammation and lung function. Our study investigated the cellular function that may be
relevant and underpin the clinical approach to lowering the dose of ICS therapy in COPD patients. We compared the single administration of low-dose ICS/LABA combination to high-dose ICS alone and high-dose ICS/LABA on GR activation, molecular markers of AJRCCM as
airway inflammation and lung function in COPD patients 2 hours post-treatment. Some of the results of these studies have been previously reported in the form of an abstract (9).
Date Issued
2019-03-01
Date Acceptance
2018-12-06
Citation
American Journal of Respiratory and Critical Care Medicine, 2019, 199 (5), pp.662-664
ISSN
1073-449X
Publisher
American Thoracic Society
Start Page
662
End Page
664
Journal / Book Title
American Journal of Respiratory and Critical Care Medicine
Volume
199
Issue
5
Copyright Statement
© 2018 American Thoracic Society.
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/30540486
Subjects
Science & Technology
Life Sciences & Biomedicine
Critical Care Medicine
Respiratory System
General & Internal Medicine
EXACERBATIONS
11 Medical and Health Sciences
Respiratory System
Publication Status
Published
Coverage Spatial
United States
Date Publish Online
2018-12-12