Applications of peptide hormone ligands for the treatment of dumping and short bowel syndrome.
Curr Opin Pharmacol · 2018
Last updated 2026-05-28A study found that pasireotide, a somatostatin analogue, improved dumping syndrome in a phase-2 trial, while the GLP-1 drug liraglutide also showed preliminary benefits. In short bowel syndrome, the GLP-2 drug teduglutide reduced the need for parenteral (IV) nutrition in patients, and other GLP-2 and GLP-1 drugs like liraglutide are being studied as potential treatments.
AI summary of the abstract below.
| Journal | Curr Opin Pharmacol, 2018 |
|---|---|
| Citations | 11 |
| Relative citation ratio | 0.70 |
| NIH percentile | 38 |
| Molecules | — |
Abstract
Dumping syndrome is a common and debilitating complication of upper gastrointestinal surgery. Accelerated gastric emptying and dysregulated secretion of gastrointestinal (GI) hormones are involved in its pathophysiology. Pasireotide, a novel somatostatin analogue, improved dumping in a phase-2 study. Preliminary data suggest that the glucagon-like peptide-1 (GLP-1) analogue liraglutide can also improve dumping. Short bowel syndrome is the most common cause of intestinal failure and involves not only a loss of mucosal absorptive area but also hypersecretion and accelerated transit. GLP-2 is the best studied hormone involved in intestinal adaptation. An increasing body of evidence demonstrates that the GLP-2 analogue teduglutide reduces parenteral support needs. New GLP-2 analogues and analogues of other GI hormones such as liraglutide are being investigated as promising treatments in short bowel syndrome.
Verbatim abstract via PubMed 30273889 ↗