Mild asthma: Lessons learned and remaining questions

被引:1
作者
Mohan, Arjun [1 ,2 ]
Lugogo, Njira L. [1 ]
机构
[1] Univ Michigan, Dept Internal Med, Div Pulm & Crit Care Med, Ann Arbor, MI USA
[2] Univ Michigan, Pulm & Crit Care Med, 300 North Ingalls St,Suite 2D21, Ann Arbor, MI 48109 USA
关键词
Mild asthma; Risks; Inflammation; Management; Future research; LEUKOTRIENE-RECEPTOR ANTAGONISTS; INHALED CORTICOSTEROID TREATMENT; BLOOD EOSINOPHIL COUNT; EXHALED NITRIC-OXIDE; BUDESONIDE-FORMOTEROL; AIRWAY INFLAMMATION; CLUSTER-ANALYSIS; DOUBLE-BLIND; SEVERE EXACERBATIONS; PRECISION MEDICINE;
D O I
10.1016/j.rmed.2023.107326
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients living with mild disease represent the largest proportion of asthma patients. There are significant challenges in proposing a definition that would best describe these patients, while also accurately identifying atrisk individuals. Current literature suggests considerable inflammatory and clinical heterogeneity within this group. Research has shown that these patients are at risk of poor control, exacerbations, lung function decline, and death. Despite conflicting data on its prevalence, eosinophilic inflammation appears to be a predictor of poorer outcomes in mild asthma. There is an immediate need to better understand phenotypic clusters in mild asthma. It is also important to understand factors that influence disease progression and remission, as it is evident that both vary in mild asthma. Guided by robust literature that supports inhaled corticosteroid-based strategies over short-acting beta-agonist (SABA) reliant regimens, the management of these patients has evolved considerably. Unfortunately, SABA use remains high in clinical practice despite strong advocacy from the Global Initiative for Asthma. Future mild asthma research should explore the role of biomarkers, develop prediction tools based on composite risk scores, and explore targeted therapies at least for at-risk individuals.
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页数:10
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