The Wiser Strategy of Using Beta-Agonists in Asthma: Mechanisms and Rationales

被引:1
|
作者
Suh, Dong In [1 ]
Johnston, Sebastian L. [1 ,2 ,3 ]
机构
[1] Imperial Coll London, Natl Heart & Lung Inst, Norfolk Pl, London W2 1PG, England
[2] Seoul Natl Univ Hosp, Dept Pediat, Seoul, South Korea
[3] Seoul Natl Univ, Coll Med, Dept Pediat, Seoul 03080, South Korea
基金
欧洲研究理事会; 英国医学研究理事会;
关键词
Asthma; adrenergic beta-2 receptor agonist; corticosteroids; inflammatory mediators; airway inflammation; adverse reactions; risk factors; safety; adherence; ELEMENT-BINDING PROTEIN; CAMP-RESPONSE ELEMENT; INHALED CORTICOSTEROIDS; BUDESONIDE-FORMOTEROL; FLUTICASONE PROPIONATE; INFLAMMATORY MEDIATORS; JAPANESE GUIDELINES; EPITHELIAL-CELLS; GENE-EXPRESSION; SPUTUM CELLS;
D O I
10.4168/aair.2024.16.3.217
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Concerns regarding the safety of beta -2 agonists have led to revisions of the major asthma guidelines to better address these issues. Although these updates allow for a combination of previous and current strategies, they may confuse clinical practitioners. Beta -2 agonists are vital for alleviating asthma symptoms by relaxing smooth muscles; however, they also pose significant risks by inducing pro -inflammatory mediators both in vitro and in vivo . In addition to the risks of overuse and symptom masking, the use of beta-agonists alone at therapeutic doses can worsen airway inflammation and enhance virus -induced inflammation during asthma exacerbation. Inhaled corticosteroids (ICS) can effectively prevent these adverse effects. With new insights into the mechanisms of these adverse events, reserving shortacting beta-agonists for acute symptom relief during exacerbations and only for those who are already on ICS or oral steroids represents a careful approach to using beta-agonists with least adverse effects in patients with asthma. However, a major drawback of this approach is the potential non-compliance with ICS, leading to beta-agonist use without the necessary counteraction by ICS. An optimal strategy, both during and outside exacerbations, would integrate beta-agonists into an anti-inflammatory regimen that includes ICS, ideally combined with the same inhaler to ensure their concurrent use where finances allow. This would maintain the beneficial effects of beta-agonists, such as bronchodilation, while preventing the adverse effects from the induction of inflammatory mediators. This method is aligned with diverse clinical settings, maximizes the safe use of beta-agonists, and supports a comprehensive guideline -compliant management strategy.
引用
收藏
页码:217 / 234
页数:18
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