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Three-year experience with GLP-2 analog in intestinal rehabilitation for pediatric-onset short bowel syndrome
Yuko Tazuke1, Takeshi Kimura2, Takehisa Ueno3
1Department of Pediatric Surgery, Hyogo Medical University, Mukogawa-Cho, Nishinomiya, Hyogo, 663-8501, Japan. ytazuke@hyo-med.ac.jp.
Insights
Glucagon-like peptide 2 (GLP-2) analog therapy reduced parenteral nutrition (PN) dependency and improved intestinal rehabilitation in short bowel syndrome (SBS) patients over three years. This therapy enhanced clinical outcomes and quality of life, especially in adults.
Area of Science:
- Gastroenterology
- Pediatric Gastroenterology
- Clinical Pharmacology
Background:
- Short bowel syndrome (SBS) is a complex condition often requiring long-term parenteral nutrition (PN).
- Intestinal rehabilitation is crucial for managing SBS and reducing PN dependency.
- Glucagon-like peptide 2 (GLP-2) analogs represent a therapeutic option to enhance intestinal adaptation.
Purpose of the Study:
- To assess the three-year impact of Glucagon-like peptide 2 (GLP-2) analog therapy on parenteral nutrition (PN) dependency.
- To evaluate the effects of GLP-2 analog therapy on intestinal rehabilitation and quality of life in pediatric-onset short bowel syndrome (SBS).
Main Methods:
- Retrospective analysis of clinical data from 18 pediatric-onset SBS patients undergoing GLP-2-based intestinal rehabilitation over three years.
- Evaluation of changes in PN requirements, serum citrulline levels, stool parameters, and quality of life indicators.
- Monitoring for adverse events and intestinal polyps.
Main Results:
- Significant reductions in PN requirements were observed, with up to 54.6% decrease in adults and 31.9% in pediatric patients.
- Improvements in serum citrulline levels indicated enhanced intestinal adaptation; stool consistency and frequency also improved.
- One adult and one pediatric patient achieved PN independence, and overall quality of life was maintained, though some pediatric patients required educational support due to ongoing PN use.
Conclusions:
- GLP-2 analog therapy, integrated with intestinal rehabilitation, leads to sustained reductions in PN dependency and improved clinical outcomes in SBS patients over three years.
- Continuous GLP-2 analog therapy shows promise for enhancing the quality of life in pediatric-onset SBS.
- The therapy was well-tolerated, with mild and self-limiting adverse events and no detected intestinal polyps.
Purpose:
To evaluate the impact of three-year Glucagon-like peptide 2 (GLP-2) analog therapy on parenteral nutrition (PN) dependency, intestinal rehabilitation, and quality of life in pediatric-onset short bowel syndrome (SBS).
Methods:
Between August 2021 and December 2024, 18 pediatric-onset SBS patients underwent GLP-2-based intestinal rehabilitation. The remaining length of the small intestine ranged from 20 to 50 cm in adults and averaged 20 cm in children. Clinical data were retrospectively analyzed over a three-year period.
Results:
PN requirements in adults decreased by up to 54.6%, with one patient achieving PN independence. Paediatric patients showed gradual reductions of up to 31.9%. Serum citrulline levels improved, suggesting enhanced intestinal adaptation. Stool consistency improved in all patients, and stool frequency decreased in six patients. PN duration per week decreased in eight patients, with one paediatric patient successfully being weaned off PN. All patients maintained social participation, though six children required special educational support due to ongoing PN use. No intestinal polyps were detected, and any adverse events were mild and self-limiting.
Conclusions:
GLP-2 analog therapy, which is based on intestinal rehabilitation, contributed to a sustained reduction in PN and enhanced clinical outcomes over three years, particularly in adult SBS patients. Continuous GLP-2 analog therapy might improve quality of life in paediatric-onset SBS.
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