TY - JOUR
T1 - New developments in the treatment of gastroparesis and functional dyspepsia
AU - Tack, Jan
AU - Camilleri, Michael
N1 - Funding Information:
Research on FD and gastroparesis continues to explore pathophysiological mechanisms and novel treatment approaches. In FD, the research focus has shifted to the potential of loss of mucosal integrity, low-grade inflammation and potentially changes in microbiota in the duodenum as emerging areas of interest. In gastroparesis, the role of macrophages in the loss of interstitial cells of Cajal as a mechanism of disease is an ongoing hot topic. We anticipate continued advances in novel treatment approaches including new prokinetic agents (acotiamide, relamorelin), anti-emetics, psychotropics including tricyclic agents for pain and therapies targeting the pylorus. Jan Tack is supported by a Methusalem grant from Leuven University.
Publisher Copyright:
© 2018
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2018/12
Y1 - 2018/12
N2 - Functional dyspepsia (FD) and gastroparesis are frequent causes of upper gastrointestinal symptoms such as postprandial fullness, early satiation, epigastric pain or burning, upper abdominal bloating, bothersome belching, nausea and vomiting. The underlying pathophysiological mechanisms are heterogeneous and involved mechanisms such as abnormal gastric motility (accommodation, emptying), visceral hypersensitivity, low grade mucosal inflammation and cellular changes in enteric nerves, muscle or interstitial cells of Cajal. Patient-reported outcomes for evaluating treatment efficacy in these conditions were recently developed and validated. Prokinetic agents, which enhance gastric motility, are used for treating both gastroparesis and FD. In FD, besides acid suppressive therapy and Helicobacter pylori eradication, neuromodulators and drugs that enhance gastric accommodation can be applied. In gastroparesis, anti-emetics may also provide symptom relief. Novel approaches under evaluation in these conditions are the fundus relaxing agents acotiamide and buspirone and the antidepressant mirtazapine in FD. For gastroparesis, recently studied agents include the prokinetic ghrelin agonist relamorelin, the prokinetic serotonergic agents velusetrag and prucalopride, the anti-emetic aprepitant and per-endoscopic pyloric myotomy procedures.
AB - Functional dyspepsia (FD) and gastroparesis are frequent causes of upper gastrointestinal symptoms such as postprandial fullness, early satiation, epigastric pain or burning, upper abdominal bloating, bothersome belching, nausea and vomiting. The underlying pathophysiological mechanisms are heterogeneous and involved mechanisms such as abnormal gastric motility (accommodation, emptying), visceral hypersensitivity, low grade mucosal inflammation and cellular changes in enteric nerves, muscle or interstitial cells of Cajal. Patient-reported outcomes for evaluating treatment efficacy in these conditions were recently developed and validated. Prokinetic agents, which enhance gastric motility, are used for treating both gastroparesis and FD. In FD, besides acid suppressive therapy and Helicobacter pylori eradication, neuromodulators and drugs that enhance gastric accommodation can be applied. In gastroparesis, anti-emetics may also provide symptom relief. Novel approaches under evaluation in these conditions are the fundus relaxing agents acotiamide and buspirone and the antidepressant mirtazapine in FD. For gastroparesis, recently studied agents include the prokinetic ghrelin agonist relamorelin, the prokinetic serotonergic agents velusetrag and prucalopride, the anti-emetic aprepitant and per-endoscopic pyloric myotomy procedures.
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U2 - 10.1016/j.coph.2018.08.015
DO - 10.1016/j.coph.2018.08.015
M3 - Review article
C2 - 30245474
AN - SCOPUS:85053798773
SN - 1471-4892
VL - 43
SP - 111
EP - 117
JO - Current Opinion in Pharmacology
JF - Current Opinion in Pharmacology
ER -