医学
哮喘
肺活量测定
内科学
过敏性
辣椒素
糖尿病
沙美特罗
受体
内分泌学
作者
Yoshihiro Kanemitsu,Kensuke Fukumitsu,Ryota Kurokawa,Norihisa Takeda,Motohiko Suzuki,Jennifer Maries Yap,Hirono Nishiyama,Tomoko Tajiri,Satoshi Fukuda,Takehiro Uemura,Hirotsugu Ohkubo,Ken Maeno,Yutaka Ito,Tetsuya Oguri,Masaya Takemura,Akio Niimi
标识
DOI:10.1164/rccm.201911-2263oc
摘要
Abstract Rationale Capsaicin cough reflex sensitivity (C-CS) is associated with poorly controlled asthma, although its association with severe asthma remains unknown. Objectives To determine the clinical impact of C-CS on severe asthma. Methods We prospectively enrolled 157 patients with asthma (including 122 patients with severe asthma who were in step 4 or 5 according to the Global Initiative for Asthma 2015 guidelines) between November 2016 and October 2019. A capsaicin cough challenge was performed along with spirometry and assessment of biomarkers. The concentration required to induce at least five coughs by capsaicin was adopted as an index of C-CS. An Asthma Control Test and comorbidities were also evaluated. Associations of biomarkers with four clinical features of severe asthma made by the European Respiratory Society/American Thoracic Society guidelines (poor control [Asthma Control Test < 20; n = 58], frequent exacerbations [≥2/yr; n = 28], admissions [≥1/yr; n = 17], and airflow limitation [FEV1% predicted < 80%; n = 30]) were assessed. Measurements and Main Results Heightened C-CS was associated with poor asthma control, frequent exacerbations, and admissions, particularly in patients without atopy (n = 54). Meanwhile, C-CS was not related to airflow limitation. Multivariate regression analysis has revealed that heightened C-CS (at least five coughs by capsaicin ≤ 2.44 μM) was a significant risk for poor asthma control and frequent exacerbations. Regarding general factors and comorbidities, ex-smoking status, diabetes mellitus, and chronic rhinosinusitis were associated with clinical features of severe asthma (all P < 0.05). Conclusions Heightened C-CS is a risk factor for severe asthma. The present study suggests the association of airway neuronal dysfunction with the pathophysiology of non–type 2 severe asthma.
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