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Updated: Mar 22, 2026

Breath Collection from Children for Disease Biomarker Discovery
Published on: February 14, 2019
Exhaled breath analysis in childhood rheumatic disorders--a longitudinal study
N Hendel1, M K Akmatov, J Hamel
1Department of Pediatrics, University Children's Hospital, Technical University Dresden, Dresden, Germany. Division of Pulmonary Medicine, University Children's Hospital, Technical University Dresden, Dresden, Germany. These authors contributed equally to this work.
Fraction of exhaled nitric oxide (FENO50) and exhaled breath condensate pH (dEBCpH) did not consistently indicate airway inflammation in pediatric rheumatologic patients. Some patients showed abnormal values of unknown significance, suggesting further research is needed.
Area of Science:
- Pediatric Rheumatology
- Pulmonary Medicine
- Biomarker Research
Background:
- Subclinical airway inflammation can occur in pediatric rheumatologic disorders.
- Non-invasive markers like FENO50 and dEBCpH are sought to assess this inflammation.
- Existing research on these markers in pediatric rheumatology is limited.
Purpose of the Study:
- To evaluate fraction of exhaled nitric oxide (FENO50) and deaerated exhaled breath condensate pH (dEBCpH) as non-invasive markers of subclinical airway inflammation.
- To assess the correlation of FENO50 and dEBCpH with disease activity and atopic sensitization in pediatric rheumatologic patients.
- To monitor changes in FENO50 and dEBCpH over a 12-month period.
Main Methods:
- Prospective study of 85 pediatric patients with rheumatologic disorders (JIA, CRMO, SLE, JDM, etc.).
- FENO50 and dEBCpH measurements were taken over at least 12 months.
- dEBCpH was also measured in 90 healthy controls; pulmonary function tests and atopic sensitization were assessed.
Main Results:
- Neither FENO50 nor dEBCpH correlated with disease activity.
- Elevated FENO50 levels were observed in 31% of patients, predominantly those with atopic sensitization.
- Median dEBCpH did not differ between patients and controls, but showed a slight decrease over time; FENO50 remained stable.
Conclusions:
- FENO50 and dEBCpH did not show consistent abnormalities in this cohort of pediatric rheumatologic patients with stable disease.
- Some patients exhibited abnormal values of unknown significance, warranting further investigation.
- These markers may not be reliable indicators of subclinical airway inflammation in this population.
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