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Published on: September 22, 2019
Overlap between irritable bowel syndrome and inflammatory bowel disease
1Nottingham Digestive Diseases Centre, Biomedical Research Unit, University Hospital, Nottingham, UK. robin.spiller@nottingham.ac.uk
Irritable bowel syndrome (IBS) involves low-grade gut inflammation, particularly mast cell activation in women. Post-infectious IBS links gut permeability changes and psychological factors to this inflammation.
Area of Science:
- Gastroenterology
- Immunology
- Microbiology
Background:
- Irritable bowel syndrome (IBS) is associated with increased colonic inflammatory cells, distinct from inflammatory bowel disease (IBD).
- This low-grade inflammation predominantly involves mast cells, especially in female IBS patients.
- Inflammation pathways include infection, stress, food allergy, and gut microbiota alterations.
Purpose of the Study:
- To investigate the characteristics and contributing factors of low-grade mucosal inflammation in IBS.
- To explore the relationship between gut permeability, visceral hypersensitivity, and post-infective IBS.
- To identify risk factors for post-infective IBS, including psychological and microbiological elements.
Main Methods:
- Analysis of colonic mucosal inflammatory cell profiles in IBS patients.
- Assessment of gut permeability in small and large bowels.
- Review of risk factors for post-infective IBS, encompassing local, microbiological, and psychological aspects.
Main Results:
- IBS mucosa exhibits inflammation quantitatively less than IBD, with a predominance of mast cells.
- Post-infectious IBS is characterized by low-grade inflammation and prolonged increases in gut permeability.
- Psychological factors like stress, anxiety, and depression are identified as risk factors for post-infective IBS.
Conclusions:
- Low-grade mucosal inflammation, particularly mast cell-driven, is a feature of IBS.
- Increased gut permeability and visceral hypersensitivity are linked to IBS, especially post-infective forms.
- Further large-scale trials are needed to validate therapeutic strategies targeting these inflammatory changes in IBS.
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