| Literature DB >> 35841222 |
Kvetoslava Rimárová1, Gabriel Samasca2, Pavol Makovický3, Petra Žáková4, Iulia Lupan5, Erik Dorko1, Jana Diabelková1, Lívia Kaňuková1, Andrej Jenča6, Adriána Petrášová6, Dana Kluková7, Ciprian Silaghi8, Peter Makovický9,10.
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.Entities:
Keywords: animal models; celiac disease; gene mutation; gluten; mouse; non-celiac gluten sensitivity; pathology; prevention; rat; small bowel
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Year: 2022 PMID: 35841222 DOI: 10.21101/cejph.a6810
Source DB: PubMed Journal: Cent Eur J Public Health ISSN: 1210-7778 Impact factor: 1.154