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Published in: Orphanet Journal of Rare Diseases 1/2006

Open Access 01-12-2006 | Review

Celiac disease

Authors: Wolfgang Holtmeier, Wolfgang F Caspary

Published in: Orphanet Journal of Rare Diseases | Issue 1/2006

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Abstract

Celiac disease is a chronic intestinal disease caused by intolerance to gluten. It is characterized by immune-mediated enteropathy, associated with maldigestion and malabsorption of most nutrients and vitamins. In predisposed individuals, the ingestion of gluten-containing food such as wheat and rye induces a flat jejunal mucosa with infiltration of lymphocytes. The main symptoms are: stomach pain, gas, and bloating, diarrhea, weight loss, anemia, edema, bone or joint pain. Prevalence for clinically overt celiac disease varies from 1:270 in Finland to 1:5000 in North America. Since celiac disease can be asymptomatic, most subjects are not diagnosed or they can present with atypical symptoms. Furthermore, severe inflammation of the small bowel can be present without any gastrointestinal symptoms. The diagnosis should be made early since celiac disease causes growth retardation in untreated children and atypical symptoms like infertility or neurological symptoms. Diagnosis requires endoscopy with jejunal biopsy. In addition, tissue-transglutaminase antibodies are important to confirm the diagnosis since there are other diseases which can mimic celiac disease. The exact cause of celiac disease is unknown but is thought to be primarily immune mediated (tissue-transglutaminase autoantigen); often the disease is inherited. Management consists in life long withdrawal of dietary gluten, which leads to significant clinical and histological improvement. However, complete normalization of histology can take years.
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Metadata
Title
Celiac disease
Authors
Wolfgang Holtmeier
Wolfgang F Caspary
Publication date
01-12-2006
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2006
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/1750-1172-1-3

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