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Published on: June 1, 2022
Faecal Volatile Organic Compound Analysis in De Novo Paediatric Inflammatory Bowel Disease by Gas Chromatography-Ion
Eva Vermeer1,2,3, Jasmijn Z Jagt1,2,3, Trenton K Stewart4
1Department of Paediatric Gastroenterology, Emma Children's Hospital, Amsterdam University Medical Centre, 1105 AZ Amsterdam, The Netherlands.
Insights
Faecal volatile organic compound (VOC) profiles distinguish paediatric inflammatory bowel disease (IBD) patients from controls. However, baseline VOC patterns did not predict treatment response in these young IBD patients.
Area of Science:
- Microbiology
- Gastroenterology
- Metabolomics
Background:
- Gut microbiota and metabolites differ in inflammatory bowel disease (IBD).
- Volatile organic compounds (VOCs) are microbial metabolites with diagnostic potential.
- Paediatric IBD patient data on VOC profiles and treatment response is limited.
Purpose of the Study:
- To compare faecal VOC profiles between paediatric IBD patients and controls with gastrointestinal symptoms (CGIs).
- To determine if baseline VOC profiles can predict treatment response in paediatric IBD patients.
Main Methods:
- Faecal samples were collected from de novo, therapy-naïve paediatric IBD patients and CGIs (aged 4-17).
- Gas chromatography-ion mobility spectrometry (GC-IMS) was used for VOC analysis.
- Treatment response was defined by clinical scores without treatment escalation.
Main Results:
- Paediatric IBD patients showed distinct faecal VOC profiles compared to CGIs (AUC 0.71, p<0.001).
- Distinct VOC profiles were observed in both Crohn's disease (AUC 0.75) and ulcerative colitis (AUC 0.67) patients.
- No significant difference in baseline VOC profiles was found between responders and non-responders (AUC 0.70, p=0.1).
Conclusions:
- Faecal VOC profiles significantly differentiate paediatric IBD patients from CGIs.
- Current VOC analysis does not predict treatment response in paediatric IBD patients.
Abstract:
The gut microbiota and its related metabolites differ between inflammatory bowel disease (IBD) patients and healthy controls. In this study, we compared faecal volatile organic compound (VOC) patterns of paediatric IBD patients and controls with gastrointestinal symptoms (CGIs). Additionally, we aimed to assess if baseline VOC profiles could predict treatment response in paediatric IBD patients. We collected faecal samples from a cohort of de novo therapy-naïve paediatric IBD patients and CGIs. VOCs were analysed using gas chromatography-ion mobility spectrometry (GC-IMS). Response was defined as a combination of clinical response based on disease activity scores, without requiring treatment escalation. We included 109 paediatric IBD patients and 75 CGIs, aged 4 to 17 years. Faecal VOC profiles of paediatric IBD patients were distinguishable from those of CGIs (AUC ± 95% CI, p-values: 0.71 (0.64-0.79), <0.001). This discrimination was observed in both Crohn's disease (CD) (0.75 (0.67-0.84), <0.001) and ulcerative colitis (UC) (0.67 (0.56-0.78), 0.01) patients. VOC profiles between CD and UC patients were not distinguishable (0.57 (0.45-0.69), 0.87). Baseline VOC profiles of responders did not differ from non-responders (0.70 (0.58-0.83), 0.1). In conclusion, faecal VOC profiles of paediatric IBD patients differ significantly from those of CGIs.
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