The Association of Lung Function, Bronchial Hyperresponsiveness, and Exhaled Nitric Oxide Differs Between Atopic and Non-atopic Asthma in Children.
10.4168/aair.2015.7.4.339
- Author:
Eunhee SHIM
1
;
Eun LEE
;
Song I YANG
;
Young Ho JUNG
;
Geun Mi PARK
;
Hyung Young KIM
;
Ju Hee SEO
;
Jinho YU
Author Information
1. Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. jyu3922@gmail.com
- Publication Type:Original Article
- Keywords:
Asthma;
atopy;
child;
lung function, bronchial hyperresponsiveness;
exhaled nitric oxide
- MeSH:
Asthma*;
Child*;
Eosinophils;
Humans;
Immunoglobulin E;
Inflammation;
Lung*;
Methacholine Chloride;
Nitric Oxide*;
Skin
- From:Allergy, Asthma & Immunology Research
2015;7(4):339-345
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Although many previous studies have attempted to identify differences between atopic asthma (AA) and non-atopic asthma (NAA), they have mainly focused on the difference of each variable of lung function and airway inflammation. The aim of this study was to evaluate relationships between lung function, bronchial hyperresponsiveness (BHR), and the exhaled nitric oxide (eNO) levels in children with AA and NAA. METHODS: One hundred and thirty six asthmatic children aged 5-15 years and 40 normal controls were recruited. Asthma cases were classified as AA (n=100) or NAA (n=36) from skin prick test results. Lung function, BHR to methacholine and adenosine-5'-monophosphate (AMP), eNO, blood eosinophils, and serum total IgE were measured. RESULTS: The AA and NAA cases shared common features including a reduced small airway function and increased BHR to methacholine. However, children with AA showed higher BHR to AMP and eNO levels than those with NAA. When the relationships among these variables in the AA and NAA cases were evaluated, the AA group showed significant relationships between lung function, BHR to AMP or methacholine and eNO levels. However, the children in the NAA group showed an association between small airway function and BHR to methacholine only. CONCLUSIONS: These findings suggest that the pathogenesis of NAA may differ from that of AA during childhood in terms of the relationship between lung function, airway inflammation and BHR.
