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.

PubMed

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.
Abstract

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