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Published on: August 7, 2017
Biomarkers of airway and systemic inflammation in obese asthmatic paediatric patients
H T Nacaroglu1, O B Gayret2, M Erol2
1Bagcilar Training and Research Hospital, Pediatric Allergy and Immunology, Istanbul, Turkey.
Insights
Obesity may not significantly alter key inflammation biomarkers in children with asthma. However, further research is needed to explore potential links between lung function and specific inflammatory markers in this population.
Area of Science:
- Pediatric Allergy and Immunology
- Respiratory Medicine
- Obesity Research
Background:
- Airway inflammation is often more challenging to manage in obese individuals with asthma.
- Obesity may exacerbate asthma severity due to altered inflammatory responses and reduced treatment efficacy.
Purpose of the Study:
- To examine the impact of obesity on airway and systemic inflammation in pediatric asthma patients.
- To identify potential biomarkers associated with inflammation in obese children with asthma.
Main Methods:
- Compared complete blood count parameters and inflammatory markers (hs-CRP, NGAL, OPN, MMP-9, 25(OH)-vitamin D) in three groups: obese asthmatic, obese non-asthmatic, and non-obese non-asthmatic children (ages 6-16).
Main Results:
- No significant differences in 25(OH)-vitamin D, NGAL, OPN, hs-CRP, or MMP-9 levels were found between the groups.
- A significant negative correlation was observed between FEV1/FVC ratio and NGAL and MMP-9 levels.
Conclusions:
- This study is the first to assess hs-CRP, NGAL, OPN, MMP-9, and 25(OH)-vitamin D in obese pediatric asthma patients.
- Larger studies incorporating sputum and bronchoalveolar lavage (BAL) are recommended to fully elucidate the role of these biomarkers in obese asthmatic children.
Background:
It is thought that airway inflammation is more common in obese asthmatic patients because inflammation is harder to control and does not respond well to glucocorticoid treatment.
Objective:
This study's aim was to investigate the effect of obesity on airway and systemic inflammation in children with asthma and to identify the biomarkers that play a role in this inflammation.
Methods:
The study included patients aged 6-16 years who were diagnosed with asthma in the paediatric allergy outpatient clinic of Bagcilar Training and Research Hospital in Turkey. Complete blood count parameters were compared between three groups: obese asthmatic (n=43), obese non-asthmatic (n=45), and non-obese non-asthmatic (control group, n=30). Levels of high-sensitive CRP (hs-CRP), neutrophil gelatinase-associated lipocalin (NGAL), osteopontin (OPN), and matrix metalloproteinase-9 (MMP-9), and 25(OH)-vitamin D were compared between the groups.
Results:
No statistically significant differences were observed in 25(OH)-vitamin D, NGAL, OPN, hs-CRP, and MMP-9 levels between groups. There was a statistically significant negative correlation between FEV1/FVC and NGAL and MMP-9.
Conclusion:
This is the first study to investigate levels of hs-CRP, NGAL, OPN, MMP-9, and 25(OH)-vitamin D in obese asthmatic children. Larger studies with sputum and BAL examinations are required to determine the potential of biomarkers for identifying inflammation in obese asthmatic children.
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