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Genetically modified rodent models and celiac, non-celiac gluten sensitivity: a minireview.
- Source :
-
Central European journal of public health [Cent Eur J Public Health] 2022 Jun; Vol. 30 Suppl, pp. S27-S31. - Publication Year :
- 2022
-
Abstract
- Celiac disease (CD) is a disorder that affects both children and adults. Over the few last decades, several new atypical cases have been identified through improved diagnostic tools. On the other hand, the onset of CD at a later age, including atypical CD forms whose clinical picture overlaps with other autoimmune diseases, shows that currently there are several unknown gene mutations, which could be responsible for the disease development. Non-celiac gluten sensitivity (NCGS) is entity included by the ingestion of gluten leading to intestinal, or extraintestinal symptoms that improve once the gluten is removed from the nutrition. In this article relationships between genetically modified rodent animals with previously unknown multiple organ changes and CD, respectively NCGS are reviewed. Relationships between the small bowel histological changes and other organs pathology are discussed. Results of research document that changes have similar genetic background and can develop to serious autoimmune systematic diseases, including small bowel inflammation resembling atypical CD or NCGS. These may have extra-intestinal symptomatology but without a clear explanation of causes and differences in their manifestations. Research on animal models helps to discover links between several disorders associated with gastrointestinal damage. New methods based on individual gene mutations can help in atypical adult CD and NCGS recognitions in the future.
- Subjects :
- Animals
Glutens
Models, Animal
Celiac Disease genetics
Rodentia
Subjects
Details
- Language :
- English
- ISSN :
- 1210-7778
- Volume :
- 30 Suppl
- Database :
- MEDLINE
- Journal :
- Central European journal of public health
- Publication Type :
- Academic Journal
- Accession number :
- 35841222
- Full Text :
- https://doi.org/10.21101/cejph.a6810