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Applications of peptide hormone ligands for the treatment of dumping and short bowel syndrome.

Curr Opin Pharmacol · 2018

Last updated 2026-05-28

A 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.

JournalCurr Opin Pharmacol, 2018
Citations11
Relative citation ratio0.70
NIH percentile38
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 ↗