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Published on: February 9, 2022
Subclinical small airway dysfunction in well-controlled asthmatic children with normal FEV1 z-score
Gökçen Kartal Öztürk1, Hazal Gacemer1, Ece Halis1
1Department of Pediatric Pulmonology, Ege University Faculty of Medicine, Izmir, Turkey.
Insights
Subclinical small airway dysfunction (SAD) may affect children with well-controlled asthma. Impulse oscillometry system (IOS) effectively detects SAD, with younger, atopic children being at higher risk.
Area of Science:
- Pediatric Pulmonology
- Respiratory Medicine
- Asthma Research
Background:
- Subclinical small airway dysfunction (SAD) is linked to asthma persistence, poor control, and exacerbations.
- Evaluating SAD in well-controlled pediatric asthma with normal spirometry is crucial.
Purpose of the Study:
- To assess subclinical SAD in children with well-controlled asthma using impulse oscillometry system (IOS).
- To identify pulmonary function test (PFT) parameters predicting SAD.
- To determine risk factors associated with SAD.
Main Methods:
- Retrospective cohort study comparing 194 asthmatic children (6-18 years) with normal FEV1 z-scores to 151 healthy controls.
- Assessed spirometry and IOS parameters.
- Utilized logistic regression and ROC curve analyses for predictive PFT parameters.
Main Results:
- Asthmatic children showed lower FEV1/FVC and FEF25-75, and altered IOS parameters (higher R5, R10, Fres, Ax, ΔR5-20; more negative X5-X20) despite normal spirometry.
- ΔR5-20 moderately predicted SAD (OR 1.086, p<0.01) with a cutoff of ≥22.15% (AUC 0.660).
- Younger age and atopy were independent risk factors for higher ΔR5-20.
Conclusions:
- Subclinical SAD is likely present in children with well-controlled asthma and normal FEV1.
- IOS, especially ΔR5-20, is a sensitive, effort-independent tool for SAD detection.
- Routine IOS evaluation is recommended for pediatric asthma, particularly in younger, atopic individuals.
Background:
This study aimed to evaluate the presence of subclinical small airway dysfunction (SAD), which is associated with risk for persistence, loss of control, and exacerbations, using the impulse oscillometry system (IOS) in children with well-controlled asthma and normal forced expiratory volume in one second (FEV1) z-scores and to identify predictive pulmonary function test (PFT) parameters and associated risk factors for SAD.
Methods:
A retrospective cohort study was conducted in children aged 6-18 years with well-controlled asthma and normal FEV1, compared to healthy controls matched for age and sex. Spirometry and IOS parameters were assessed. Logistic regression and receiver operating characteristic (ROC) curve analyses were used to determine predictive PFT parameters.
Results:
A total of 194 asthmatic children and 151 healthy controls were included. Although spirometry parameters were within normal limits, FEV1/FVC and FEF25-75 (% predicted and z-scores) were significantly lower in the asthma group (p < .01). IOS parameters, including R5, R10, Fres, Ax, and ΔR5-20, were significantly higher in asthmatic children (p < .05), and reactance values (X5-X20) were more negative. ΔR5-20 was the moderately predictive parameter for SAD [OR (95% CI): 1.086 (1.017-1.159), p < .01] with a cutoff value of ≥22.15% (AUC 0.660, sensitivity 60%, specificity 68%). Younger age and atopy were independent risk factors for higher ΔR5-20.
Conclusion:
Subclinical SAD may be present in children with well-controlled asthma and normal FEV1. IOS, particularly ΔR5-20, provides a sensitive, effort-independent tool for detecting SAD and should be considered for routine evaluation, especially in younger and atopic children.
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