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Published on: May 15, 2013
Effect of age on relationship between exhaled nitric oxide and airway hyperresponsiveness in asthmatic children
Chikako Motomura1, Hiroshi Odajima1, Junichiro Tezuka1
1Department of Pediatrics, Fukuoka National Hospital, Minami-ku, Fukuoka, Japan.
Insights
In children with asthma, airway hyperresponsiveness (AHR) correlates with airway inflammation, indicated by fractional exhaled nitric oxide (Feno). In adolescents, AHR is linked to structural changes, with a weaker association with inflammation.
Area of Science:
- Pediatric Pulmonology
- Respiratory Medicine
- Allergy and Immunology
Background:
- Fractional exhaled nitric oxide (Feno) and airway hyperresponsiveness (AHR) are key asthma indicators.
- Age-related differences in the Feno-AHR relationship in pediatric asthma are not fully understood.
Purpose of the Study:
- To investigate how age influences the association between Feno and AHR in children with asthma.
- To differentiate the underlying mechanisms of AHR in younger children versus adolescents with asthma.
Main Methods:
- Studied 267 asthmatic patients aged 5-20 years.
- Assessed AHR using acetylcholine challenge tests to determine provocative concentration (PC(20)).
- Measured Feno using the online method prior to the challenge test.
Main Results:
- In children under 12, lower PC(20) (indicating AHR) strongly correlated with higher Feno levels.
- In adolescents (12-20 years), lower PC(20) was associated with peripheral airway obstruction, with a weak correlation to Feno.
- AHR in adolescents showed associations with FEV(1) and FVC parameters, suggesting structural changes.
Conclusions:
- In pediatric asthma, AHR is primarily linked to airway inflammation, reflected by Feno.
- In adolescent asthma, AHR appears to involve airway remodeling and structural changes, with inflammation playing a lesser role.
- Age is a critical factor in understanding the pathophysiology of AHR in asthma.
Background:
Numerous studies have examined the relationship between the fractional concentration of exhaled nitric oxide (Feno) and airway hyperresponsiveness (AHR). Our objective was to determine the effects of age on the relationship between Feno and AHR in asthmatic children.
Methods:
AHR was examined in 267 asthmatic patients (age range, 5 to 20 years). A challenge test was performed using acetylcholine chloride (Ach). We determined the provocative concentration of Ach producing a 20% decrease in FEV(1) from baseline (PC(20)). Feno was examined using the recommended online method before the Ach challenge test.
Results:
In children < 12 years of age (range, 5 to 11 years), decreasing AHR (PC(20)) was significantly related to higher Feno (r = -0.43; beta = -0.28; p < 0.001). In adolescents >or= 12 years of age (range, 12 to 20 years), decreasing PC(20) was associated with peripheral airway obstruction (FEV(1): r = 0.32; beta = 5.5; p = 0.002; forced expiratory flow at 50% of the FVC: r = 0.24; beta=8.4; p = 0.006; and forced expiratory flow at 25% of FVC: r = 0.28; beta=11.4; p = 0.002). AHR and Feno were weakly related (r = -0.18; beta = -0.14; p = 0.02).
Conclusions:
In children with asthma, AHR is associated with airway inflammation. AHR in children with asthma may consist of variable components mainly reflecting airway inflammation. In contrast, in adolescents with asthma, AHR is associated with airway structural changes and weakly with airway inflammation. AHR in adolescents with asthma may consist of chronic components mainly reflecting airway remodeling.
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