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Updated: May 10, 2025

Breath Collection from Children for Disease Biomarker Discovery
Published on: February 14, 2019
Uncovering Non-Invasive Biomarkers in Paediatric Severe Acute Asthma Using Targeted Exhaled Breath Analysis
Sarah van den Berg1,2, Annabel S Zaat3, Isabel F van der Poel3
1Paediatric Intensive Care Unit, Emma Children's Hospital, Amsterdam University Medical Centre, Location AMC, 1105 AZ Amsterdam, The Netherlands.
Insights
Exhaled breath analysis can identify specific volatile organic compounds (VOCs) in children with severe acute asthma (SAA). This non-invasive method shows promise for early detection and intervention in pediatric asthma patients.
Area of Science:
- Pediatric Pulmonology
- Metabolomics
- Biomarker Discovery
Background:
- Severe acute asthma (SAA) in children presents a growing challenge, with increasing pediatric intensive care unit (PICU) admissions.
- The complex pathophysiology of asthma requires further exploration to understand its heterogeneous nature.
Purpose of the Study:
- To evaluate the utility of non-invasive targeted exhaled breath metabolomics for characterizing SAA in children.
- To identify potential biomarkers for early recognition and intervention in pediatric severe asthma.
Main Methods:
- Utilized thermal desorption gas chromatography-mass spectrometry (TD-GC-MS) to analyze breath samples.
- Compared volatile organic compound (VOC) profiles from 17 children with SAA (cases) against 27 children with controlled severe asthma (controls).
Main Results:
- Identified 25 VOCs, with 16 common to both groups.
- Found four VOCs more frequently present and nine VOCs at higher concentrations in children with SAA.
- Longitudinal analysis of 10 cases confirmed the reproducibility of identified VOC biomarkers.
Conclusions:
- Exhaled breath analysis offers valuable insights into the molecular underpinnings of SAA.
- Breath metabolomics holds potential for early detection of severe asthma exacerbations and guiding preventive therapies in children.
Background:
Severe acute asthma (SAA) in children can be life-threatening. There has been a significant rise in paediatric intensive care unit (PICU) admissions due to SAA over the past two decades. While asthma is a heterogeneous disease, its underlying pathophysiological pathways remain underexplored. This study aimed to assess the value of non-invasive targeted exhaled breath metabolomics analysis to better characterise SAA.
Methods:
Breath samples from 17 children admitted to the PICU with SAA (cases) and 27 children with controlled severe asthma (controls) were analysed using thermal desorption gas chromatography-mass spectrometry (TD-GC-MS).
Results:
A targeted volatile organic compound (VOC) analysis identified 25 compounds, of which 16 were shared between groups. Four VOCs were significantly more often present in SAA, and nine VOCs exhibited higher concentrations in SAA. Longitudinal analysis of VOCs from follow-up samples of 10 cases showed no significant temporal differences, reinforcing the reproducibility of identified biomarkers.
Conclusions:
This study exemplifies the potential of exhaled breath analysis to provide insights into the molecular background of SAA. Breath metabolomics may enable early recognition of severe asthma attacks and preventive therapeutic interventions in children with severe asthma.
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