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Beta-blockers: friend or foe in asthma?

BACKGROUND AND AIM: Recently, β-blockers have been suggested as a potential maintenance treatment option for asthma. The aim of this review is to provide an overview of the current knowledge of the potential benefits and risks of β-blocker therapy for asthma. METHOD: Systematic literature review. RE...

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Autores principales: Arboe, Bente, Ulrik, Charlotte Suppli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709648/
https://www.ncbi.nlm.nih.gov/pubmed/23882156
http://dx.doi.org/10.2147/IJGM.S46592
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author Arboe, Bente
Ulrik, Charlotte Suppli
author_facet Arboe, Bente
Ulrik, Charlotte Suppli
author_sort Arboe, Bente
collection PubMed
description BACKGROUND AND AIM: Recently, β-blockers have been suggested as a potential maintenance treatment option for asthma. The aim of this review is to provide an overview of the current knowledge of the potential benefits and risks of β-blocker therapy for asthma. METHOD: Systematic literature review. RESULTS: No significant increase in the number of patients requiring rescue oral corticosteroid for an exacerbation of asthma has been observed after initiation of β-blocker treatment. Patients with mild to moderate reactive airway disease, probably both asthma and chronic obstructive pulmonary disease, may have a limited fall in forced expiratory volume in 1 second (FEV(1)) following single-dose administration of β-blocker, whereas no change in FEV(1) has been reported following long-term administration. In a murine model of asthma, long-term administration of β-blockers resulted in a decrease in airway hyperresponsiveness, suggesting an anti-inflammatory effect. In keeping with this, long-term administration of a nonselective β-blocker to steroid-naïve asthma patients has shown a dose-dependent improvement in airway hyperresponsiveness, and either an asymptomatic fall in FEV(1) or no significant change in FEV(1). Furthermore, available studies show that bronchoconstriction induced by inhaled methacholine is reversed by salbutamol in patients on regular therapy with a β-blocker. On the other hand, a recent placebo-controlled trial of propranolol and tiotropium bromide added to inhaled corticosteroids revealed no effect on airway hyperresponsiveness and a small, not statistically significant, fall in FEV(1) in patients classified as having mild to moderate asthma. CONCLUSION: The available, although limited, evidence suggests that a dose-escalating model of β-blocker therapy to patients with asthma is well tolerated, does not induce acute bronchoconstriction, and, not least, may have beneficial effects on airway inflammation and airway hyperresponsiveness in some patients with asthma. Further studies addressing the potential role of β-blocker therapy for asthma are clearly needed, but careful selection of the target population is warranted.
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spelling pubmed-37096482013-07-23 Beta-blockers: friend or foe in asthma? Arboe, Bente Ulrik, Charlotte Suppli Int J Gen Med Review BACKGROUND AND AIM: Recently, β-blockers have been suggested as a potential maintenance treatment option for asthma. The aim of this review is to provide an overview of the current knowledge of the potential benefits and risks of β-blocker therapy for asthma. METHOD: Systematic literature review. RESULTS: No significant increase in the number of patients requiring rescue oral corticosteroid for an exacerbation of asthma has been observed after initiation of β-blocker treatment. Patients with mild to moderate reactive airway disease, probably both asthma and chronic obstructive pulmonary disease, may have a limited fall in forced expiratory volume in 1 second (FEV(1)) following single-dose administration of β-blocker, whereas no change in FEV(1) has been reported following long-term administration. In a murine model of asthma, long-term administration of β-blockers resulted in a decrease in airway hyperresponsiveness, suggesting an anti-inflammatory effect. In keeping with this, long-term administration of a nonselective β-blocker to steroid-naïve asthma patients has shown a dose-dependent improvement in airway hyperresponsiveness, and either an asymptomatic fall in FEV(1) or no significant change in FEV(1). Furthermore, available studies show that bronchoconstriction induced by inhaled methacholine is reversed by salbutamol in patients on regular therapy with a β-blocker. On the other hand, a recent placebo-controlled trial of propranolol and tiotropium bromide added to inhaled corticosteroids revealed no effect on airway hyperresponsiveness and a small, not statistically significant, fall in FEV(1) in patients classified as having mild to moderate asthma. CONCLUSION: The available, although limited, evidence suggests that a dose-escalating model of β-blocker therapy to patients with asthma is well tolerated, does not induce acute bronchoconstriction, and, not least, may have beneficial effects on airway inflammation and airway hyperresponsiveness in some patients with asthma. Further studies addressing the potential role of β-blocker therapy for asthma are clearly needed, but careful selection of the target population is warranted. Dove Medical Press 2013-07-08 /pmc/articles/PMC3709648/ /pubmed/23882156 http://dx.doi.org/10.2147/IJGM.S46592 Text en © 2013 Arboe and Ulrik, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Arboe, Bente
Ulrik, Charlotte Suppli
Beta-blockers: friend or foe in asthma?
title Beta-blockers: friend or foe in asthma?
title_full Beta-blockers: friend or foe in asthma?
title_fullStr Beta-blockers: friend or foe in asthma?
title_full_unstemmed Beta-blockers: friend or foe in asthma?
title_short Beta-blockers: friend or foe in asthma?
title_sort beta-blockers: friend or foe in asthma?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709648/
https://www.ncbi.nlm.nih.gov/pubmed/23882156
http://dx.doi.org/10.2147/IJGM.S46592
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