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Published on: April 13, 2010
Airway hyper-responsiveness to adenosine 5'-monophosphate in preschool-age children with asthma
1Gazi University, Faculty of Medicine, Department of Pediatric Allergy and Asthma, Ankara, Turkey. arzub@gazi.edu.tr
Insights
Peripheral blood eosinophilia predicts airway hyper-responsiveness to adenosine 5'-monophosphate (AMP) in young asthmatic children. This contrasts with atopy markers, offering a key insight for predicting AMP responsiveness in pediatric asthma.
Area of Science:
- Pediatric Pulmonology
- Allergy and Immunology
- Respiratory Medicine
Background:
- Airway hyper-responsiveness (AHR) to adenosine 5 extapostrophe-monophosphate (AMP) is linked to airway inflammation in asthma.
- Not all asthmatic patients exhibit AMP responsiveness, necessitating identification of predictive factors.
Purpose of the Study:
- To investigate predictive factors for AHR to AMP in preschool-aged children with asthma.
- To assess the relationship between AMP responsiveness and atopy, immunoglobulin E (IgE) levels, and eosinophilia.
Main Methods:
- Retrospective analysis of 63 asthmatic children (3-6 years old) challenged with AMP.
- Evaluated skin-prick tests, serum IgE, peripheral blood eosinophil percentage, and bronchial challenges with methacholine (MCH) and AMP.
Main Results:
- 46% of children showed AHR to AMP; 93.7% showed AHR to MCH.
- Peripheral blood eosinophilia was the sole significant predictor of AMP responsiveness (OR: 5.14, p=0.025).
- AMP-responsive children had higher median serum IgE levels and more frequent peripheral blood eosinophilia compared to non-responsive children.
Conclusions:
- Peripheral blood eosinophilia can predict AMP responsiveness in preschool-aged asthmatic children.
- Atopy markers are not reliable predictors of AMP responsiveness in this age group.
- Findings suggest eosinophil count is a valuable clinical indicator for predicting AMP AHR in young asthmatics.
Abstract:
Airway hyper-responsiveness (AHR) to adenosine 5'-monophosphate (AMP) is closely associated with airway inflammation; however, not all asthmatic patients are responsive to it. This study was planned to investigate the predictive factors of AHR to AMP in asthmatic children aged between 3 and 6 yr. We performed a retrospective analysis of data from 63 asthmatic preschool-age children who were challenged by AMP in our department. All children were characterized by skin-prick tests, serum immunoglobulin E (IgE) levels, peripheral blood eosinophil percentage and bronchial challenge with methacholine (MCH) and AMP. Potential determinants for AHR to AMP were assessed within the group. AHR to AMP was found in 46% of preschool-age children with asthma, while that of MCH was 93.7%. All children responsive to AMP were also responsive to MCH. The geometric mean provocative concentration of MCH and AMP causing a 15% fall in transcutaneous oxygen tension (PC(15)PtcO(2)MCH and AMP) were 0.55 mg/ml (0.004-9.19) and 10.53 mg/ml (0.59-342.89), respectively. AMP-responsive children did not differ from non-responsive ones with respect to demographic factors, geometric mean PC(15)PtcO(2)MCH and atopic status. The median serum IgE level was significantly higher in AMP-responsive group than the non-responsive ones (p = 0.011). The peripheral blood eosinophilia was more frequent among responsive children (p = 0.019), and it was found as the only predictive factor for AMP responsiveness in preschool-age children with asthma in logistic regression model (odds ratio: 5.14; 95% CI: 1.23-21.47; p = 0.025). AMP responsiveness may be predicted by peripheral blood eosinophilia but not with atopy markers in young children with asthma.
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