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Expired nitric oxide and airway reactivity in infants at risk for asthma
Robert S Tepper1, Conrado J Llapur2, Marcus H Jones3
1Department of Pediatrics, Indiana University Medical Center, James Whitcomb Riley Hospital for Children, Wells Center for Pediatric Research, Indianapolis, Ind.
Insights
Atopic infants, even without wheezing, show altered airway function. Specific food sensitization is linked to lower airflow and increased airway reactivity, suggesting early airway involvement in atopy.
Area of Science:
- Pediatric Allergy and Immunology
- Respiratory Medicine
- Neonatal Asthma Research
Background:
- Family history of atopy, atopic dermatitis, and food allergies are known infant asthma risk factors.
- Atopic sensitization is implicated in asthma development, but early airway involvement remains unclear.
Purpose of the Study:
- To investigate if atopic infants without prior wheezing exhibit elevated expired nitric oxide (eNO) and heightened airway reactivity.
- To explore the relationship between infant atopy and early airway physiological changes.
Main Methods:
- Recruited infants with eczema; defined atopic status via specific IgE and total IgE levels.
- Measured eNO, forced expiratory flow at 75% exhaled volume (FEF75), and methacholine airway reactivity in sedated infants.
- Quantified airway reactivity using the provocative concentration to decrease FEF75 by 30% (PC30).
Main Results:
- Infants sensitized to egg/milk showed lower FEF75 and PC30 compared to non-sensitized infants.
- Higher total serum IgE levels (>20 IU/mL) correlated with increased eNO levels.
- No significant differences in eNO were found between food-sensitized and non-sensitized infants.
Conclusions:
- Atopic characteristics in infants may significantly influence airway physiology, including forced expiratory flows and reactivity.
- Findings suggest early airway involvement in the atopic process, even before wheezing occurs.
- eNO levels appear linked to overall atopic burden (total IgE) rather than specific food sensitization.
Background:
Family histories of atopy, as well as histories of atopic dermatitis and food allergy, are important risk factors for an infant to have asthma. Although atopic sensitization appears to contribute to the development of asthma, it is unclear when the airways become involved with the atopic process and whether airway function relates to the atopic characteristics of the infant.
Objective:
We sought to evaluate whether atopic infants without prior episodes of wheezing have increased expired nitric oxide (eNO) levels and heightened airway reactivity.
Methods:
Infants with eczema were recruited, and atopic status was defined by specific IgE levels to foods or aeroallergens and total IgE levels. eNO, forced expiratory flow at 75% exhaled volume (FEF(75)), and airway reactivity to inhaled methacholine were measured in sedated infants. Airway reactivity was quantified by using the provocative concentration to decrease FEF(75) by 30%.
Results:
Median age for the 114 infants evaluated was 10.7 months (range, 2.6-19.1 months). Infants sensitized to egg or milk compared with infants sensitized to neither egg nor milk had lower flows (FEF(75): 336 vs 285 mL/s, P < .003) and lower lnPC(30) (mg/mL) provocative concentrations to decrease FEF(75) by 30% (-0.6 vs -1.2, P < .02) but no difference in eNO levels. Infants with total serum IgE levels of greater than 20 IU/mL had higher eNO levels compared with infants with IgE levels of 20 IU/mL or less (14.6 vs 11.2 ppb, P < .023) but no difference in forced flows or airway reactivity.
Conclusions:
Our findings suggest that atopic characteristics of the infant might be important determinants of the airway physiology of forced expiratory flows, airway reactivity, and eNO.
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