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Published on: February 3, 2016
Impaired gastric emptying and small bowel transit in children with mitochondrial disorders
Jatinder Bhardwaj1, David Q Wan, Mary Kay Koenig
1Department of Pediatrics, University of Texas Health Science Center at Houston Medical School, Houston, TX 77030, USA. jeetu_bhardwaj@yahoo.com
Insights
Children with mitochondrial disorders often experience delayed gastric emptying and prolonged intestinal transit. Prokinetic therapy showed limited effectiveness in improving these gastrointestinal issues.
Area of Science:
- Pediatric Gastroenterology
- Mitochondrial Disorders
- Gastrointestinal Motility
Background:
- Gastrointestinal (GI) symptoms are common in children with mitochondrial disorders (MD).
- Gastric emptying (GE) and intestinal transit time (ITT) are key indicators of GI motility.
- Understanding these parameters is crucial for managing MD patients.
Purpose of the Study:
- To evaluate GE and ITT in pediatric patients with MD.
- To assess the efficacy of prokinetic agents in children with delayed GE.
Main Methods:
- 26 children (3-18 years) with MD and GI symptoms underwent scintigraphy to assess GE and ITT.
- Delayed GE defined as half emptying time >90 min (solid) or >60 min (semisolid).
- ITT defined as >4 hours for tracer mouth-to-cecum transit. Prokinetics were administered to those with delayed GE.
Main Results:
- 18/26 (69%) children had delayed GE; 12/26 (46%) had prolonged ITT.
- In 9 subjects treated with prokinetics, GE normalized in only 3.
- Abdominal pain scores did not significantly improve with prokinetic therapy.
Conclusions:
- Children with MD and GI symptoms exhibit a high prevalence of delayed GE and prolonged ITT.
- Prokinetic therapy demonstrated limited efficacy in normalizing GE or improving GI symptoms in this cohort.
- Further research into alternative therapeutic strategies for GI dysmotility in MD is warranted.
Objectives:
The primary aim of our study was to evaluate gastric emptying (GE) and intestinal transit time (ITT) in children with mitochondrial disorders (MD), and secondarily to evaluate the effect of prokinetics in those with prolonged GE.
Methods:
We enrolled subjects 3 to 18 years with MD and having any of the following gastrointestinal (GI) symptoms: abdominal pain, vomiting, constipation, diarrhea, or gastroesophageal reflux. Abdominal pain was scored by visual analog pain scale (1-10). Age-appropriate diet was labeled with radioactive technetium-99 sulfur colloid and its movement tracked along the GI tract. Delayed GE based on our institutional standards was defined as half emptying time >90 minutes for a solid and >60 minutes for a semisolid meal. Prolonged ITT was defined as >4 hours for the tracer to pass from mouth to cecum. A prokinetic was instituted to those with delayed GE, and the study was repeated if possible in 4 to 8 weeks.
Results:
Of the 26 subjects, 18 (69%) had delayed GE (median GE 99 minutes) and 12 (46%) had prolonged ITT. The study was repeated in 9 subjects after administering a prokinetic for >1 month. GE normalized in only 3 subjects (median GE on treatment 128 minutes). Mean abdominal pain score, which was 4.8 (max 10) in the 9 subjects, did not improve (5.6 after prokinetic therapy).
Conclusions:
A high prevalence of delayed GE and prolonged ITT was seen in children with MD having GI symptoms, and these abnormalities were poorly responsive to prokinetic therapy.
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