Exhaled breath condensate pH measurement in children with asthma, allergic rhinitis and atopic dermatitis
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Updated: Jul 20, 2026

Breath Collection from Children for Disease Biomarker Discovery
Published on: February 14, 2019
Luigia Brunetti1, Ruggiero Francavilla, Riccardina Tesse
1Department of Biomedicina dell'Età Evolutiva, University of Bari, Bari, Italy. l.brunetti@pediatria3.uniba.it
Insights
Exhaled breath condensate pH is a promising marker for asthma monitoring in children. Lower pH indicates airway inflammation in acute asthma, allergic rhinitis, and atopic dermatitis, normalizing with treatment.
Area of Science:
- Pediatric Pulmonology
- Allergy and Immunology
- Biomarker Discovery
Background:
- Asthma exacerbations are linked to exhaled breath condensate (EBC) pH.
- Allergic rhinitis and atopic dermatitis are known risk factors for asthma development (atopic march).
Purpose of the Study:
- To investigate EBC pH as a monitoring tool for asthma in atopic children.
- To assess EBC pH in children with allergic rhinitis and atopic dermatitis.
Main Methods:
- Collected EBC from children with acute asthma, stable asthma, allergic rhinitis, atopic dermatitis, and healthy controls.
- Measured EBC pH using a pH meter and correlated with lung function tests.
Main Results:
- Children with acute asthma, stable asthma, allergic rhinitis, and atopic dermatitis exhibited lower EBC pH than controls.
- EBC pH in acute asthma patients normalized after anti-inflammatory treatment.
- A positive correlation was observed between EBC pH and lung function (FEV1) in acute asthma.
Conclusions:
- EBC pH is a potential biomarker for assessing airway inflammation and treatment response in pediatric asthma.
- Airway acidification is evident in children with allergic rhinitis and atopic dermatitis.
- EBC pH monitoring may aid in evaluating atopic march progression and predicting future asthma development.
Abstract:
Recent studies have shown that the pH of exhaled breath condensate (EBC) could be predictive of asthma exacerbation. Moreover, it has been documented that both allergic rhinitis and atopic dermatitis constitute risk factors for the occurrence of asthma in a progression of disease known as atopic march. The aim of our study was to establish if condensate pH could be used as a valuable mean of monitoring of asthma in atopic children. We studied 34 atopic children with acute asthma, 70 with stable asthma, 35 children with allergic rhinitis, and 17 with atopic dermatitis. Thirty healthy children were used as controls. All children underwent skin prick tests and lung function tests. Exhaled breath condensate samples were collected with a condensing device and de-aerated with argon. The pH of EBC was measured using a pH meter. Children with acute asthma were treated with inhaled steroids and bronchodilators. We found that the pH of condensate in patients with acute asthma was lower than that of patients with stable asthma, rhinitis, and controls (7.25 vs. 7.32, p < 0.05; 7.25 vs. 7.48, p < 0.02; 7.25 vs. 7.78, p < 0.0001, respectively). Patients with stable asthma, rhinitis, and eczema had also lower pH than that of controls (7.32, 7.48, and 7.44 vs. 7.78; p < 0.0001, p < 0.006, p < 0.04, respectively). Patients with acute asthma normalized their pH after treatment (7.82 vs. 7.25; p < 0.0001). Finally, patients with acute asthma showed a positive correlation between pH and lung functional parameters (forced expiratory volume in 1 s; r = 0.39, p = 0.04). Our study shows that EBC pH measurement may be a promising marker for assessing airway inflammation and monitoring response to anti-inflammatory treatment in asthmatic children. Furthermore, we report the first evidence of airways acidification in children with allergic rhinitis and atopic dermatitis. Therefore, EBC pH assessment may be useful in the evaluation of progression of the atopic march toward the development of asthma later in life. Further studies are recommended in order to confirm this indication.
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