Delayed orocecal transit in pediatric gut-brain interaction disorders: A comparative study using the lactulose breath
Niranga Manjuri Devanarayana1, Shaman Rajindrajith2, Delpechitracharige Gajabahu Harendra de Silva2
1Department of Physiology, Faculty of Medicine, University of Kelaniya, Ragama 11010, Western Province, Sri Lanka. niranga@kln.ac.lk.
Children with functional abdominal pain disorders (FAPDs) exhibit prolonged orocecal transit time (OCTT) compared to healthy peers. However, delayed small intestinal transit may not be the primary driver of FAPD symptoms.
Area of Science:
- Pediatric Gastroenterology
- Gut-Brain Interaction Disorders
- Digestive Physiology
Background:
- Functional abdominal pain disorders (FAPDs) are prevalent gut-brain interaction disorders with incompletely understood pathophysiology.
- Impaired gastrointestinal motility, particularly small intestinal dysmotility, is implicated but understudied.
- Orocecal transit time (OCTT) serves as an indirect measure of small intestinal transit, offering insights into FAPD mechanisms.
Purpose of the Study:
- To compare OCTT in children diagnosed with FAPDs against healthy controls.
- To utilize the lactulose breath hydrogen test for assessing small intestinal transit.
Main Methods:
- The study included 34 children with FAPDs (Rome IV criteria) and 19 healthy controls, aged 5-12 years.
- Orocecal transit time (OCTT) was measured using a validated lactulose breath hydrogen test after an overnight fast.
- Breath hydrogen levels were monitored for 180 minutes post-ingestion to determine OCTT.
Main Results:
- Children with FAPDs demonstrated significantly longer OCTT (median 90 minutes) than healthy controls (median 75 minutes) (P=0.0045).
- Children with functional dyspepsia showed the longest mean OCTT (110.8 ± 26.7 minutes).
- No significant correlation was found between abdominal pain severity, stress exposure, and OCTT.
Conclusions:
- Pediatric FAPDs are associated with delayed small intestinal transit as indicated by prolonged OCTT.
- The absence of a strong correlation between OCTT and symptom severity suggests that delayed transit is not the sole or primary factor in FAPD pathophysiology.
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