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.
Copyright © 2018 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Animals
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Dumping Syndrome / drug therapy*
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Dumping Syndrome / metabolism
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Dumping Syndrome / physiopathology
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Gastrointestinal Agents / adverse effects
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Gastrointestinal Agents / therapeutic use*
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Gastrointestinal Motility / drug effects*
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Gastrointestinal Tract / drug effects*
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Gastrointestinal Tract / metabolism
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Gastrointestinal Tract / physiopathology
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Humans
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Intestinal Absorption / drug effects*
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Ligands
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Liraglutide / therapeutic use
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Peptides / therapeutic use
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Receptors, Gastrointestinal Hormone / drug effects*
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Receptors, Gastrointestinal Hormone / metabolism
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Short Bowel Syndrome / drug therapy*
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Short Bowel Syndrome / metabolism
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Short Bowel Syndrome / physiopathology
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Signal Transduction / drug effects
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Somatostatin / analogs & derivatives
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Somatostatin / therapeutic use
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Treatment Outcome
Substances
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Gastrointestinal Agents
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Ligands
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Peptides
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Receptors, Gastrointestinal Hormone
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Somatostatin
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teduglutide
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Liraglutide
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pasireotide