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Published on: June 29, 2019
Duodenal inflammation: an emerging target for functional dyspepsia?
Lucas Wauters1,2, Grace Burns3, Matthias Ceulemans1
1Translational Research in Gastrointestinal Diseases (TARGID), KU Leuven, Leuven, Belgium.
Functional dyspepsia (FD) involves duodenal inflammation, particularly the eosinophil-mast cell axis. Future treatments may target inflammation and gut microbiome imbalances for better symptom relief.
Area of Science:
- Gastroenterology
- Immunology
- Pharmacology
Background:
- Functional dyspepsia (FD) is a common gastrointestinal disorder with limited effective therapies.
- Duodenal inflammation and the eosinophil-mast cell axis are implicated in FD pathogenesis.
- Current treatments like prokinetics and neuromodulators have limited efficacy and side effects.
Purpose of the Study:
- To review recent advances in FD pathophysiology and treatment.
- To identify potential therapeutic targets and research gaps in FD management.
- To explore the role of inflammation and the gut microbiome in FD.
Main Methods:
- A narrative review of the literature.
- Electronic literature search conducted in PubMed up to December 31, 2019.
Main Results:
- Compelling evidence supports duodenal inflammation and the eosinophil-mast cell axis in FD.
- Proton pump inhibitors may exert therapeutic effects via anti-inflammatory actions, independent of acid suppression.
- Existing and novel anti-inflammatory drugs warrant investigation for FD.
Conclusions:
- Targeting duodenal inflammation and the eosinophil-mast cell axis is crucial for FD treatment.
- Further research into probiotics, antibiotics, and treatments for impaired permeability and dysbiosis is needed.
- Future FD therapies may focus on modulating the gut microbiome and immune activation.
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