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Published on: August 7, 2017
Airway and systemic inflammation in obese children with asthma
Megan E Jensen1, Peter G Gibson, Clare E Collins
1Hunter Medical Research Institute, Newcastle.
Insights
Obesity in childhood asthma did not significantly alter airway or systemic inflammation. However, obese girls with asthma showed a higher prevalence of non-eosinophilic asthma, requiring further study.
Area of Science:
- Pediatric Pulmonology
- Asthma Research
- Obesity and Health
Background:
- Obese asthma involves altered airway and systemic inflammation in adults.
- Comprehensive data on pediatric obese asthma inflammation is lacking.
- This study investigates inflammation differences in obese versus nonobese asthmatic children.
Purpose of the Study:
- To compare airway and systemic inflammation in obese and nonobese asthmatic children and controls.
- To assess the impact of obesity on inflammatory biomarkers in pediatric asthma.
- To explore differences in asthma phenotypes related to obesity in children.
Main Methods:
- Cross-sectional study design.
- Inclusion of four groups: obese asthma (OA), nonobese asthma (NOA), obese control (OC), and nonobese control (NOC).
- Measurement of lung function, sputum, and systemic inflammatory biomarkers in children aged 8-17 years.
Main Results:
- Obesity was linked to significant lung restriction in children, with or without asthma.
- No significant differences in airway or systemic inflammation were found between obese and nonobese asthmatic children.
- Higher prevalence of non-eosinophilic asthma observed in obese asthmatic females compared to males.
- Leptin levels were higher in obese controls, while adiponectin was reduced in obese asthmatics.
Conclusions:
- Obesity is associated with lung restriction in children, irrespective of asthma status.
- Obesity does not appear to significantly alter airway or systemic inflammation in pediatric asthma.
- The increased prevalence of non-eosinophilic asthma in obese females warrants further investigation.
Abstract:
Obese asthma presents via altered airway and systemic inflammation in adults. This has not been comprehensively described in children. The aim of the present study was to compare airway and systemic inflammation in obese and nonobese asthmatic children and controls. In a cross-sectional study, children aged 8-17 years were assigned to one of four groups: obese asthma (OA, n=74); nonobese asthma (NOA, n=249); obese control (OC, n=9); nonobese control (NOC, n=29). Lung function, and both sputum and systemic inflammatory biomarkers were measured. Non-eosinophilic asthma was more prevalent among OA females (60.0%) versus OA males (30.8%). However, there were no differences in the percentage of eosinophils or neutrophils between OA and NOA. Leptin was higher in OC, but not OA, versus NOA and NOC, while adiponectin was reduced in OA versus NOC only. Expiratory reserve volume was reduced in OA, versus NOC. Residual volume (RV) and RV/total lung capacity were reduced in OC versus OA, and OC versus OA and NOA, respectively. Obesity was associated with significant lung restriction in children with and without asthma. Obesity was not associated with significantly altered airway or systemic inflammation in asthmatic children. However, the higher prevalence of non-eosinophilic asthma in female obese asthmatics, compared to males, warrants further investigation.
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