Correlation between antibodies and histology in celiac disease: incidence of celiac disease is higher than expected in the pediatric population
Language English Country Greece Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
23942815
DOI
10.3892/mmr.2013.1627
Knihovny.cz E-resources
- MeSH
- Celiac Disease blood epidemiology immunology MeSH
- Child MeSH
- Duodenum immunology pathology MeSH
- Immunoglobulin A blood MeSH
- Immunoglobulin G blood MeSH
- Incidence MeSH
- Muscle Fibers, Skeletal immunology MeSH
- Humans MeSH
- Protein Glutamine gamma Glutamyltransferase 2 MeSH
- GTP-Binding Proteins immunology MeSH
- Transglutaminases immunology MeSH
- Check Tag
- Child MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Immunoglobulin A MeSH
- Immunoglobulin G MeSH
- Protein Glutamine gamma Glutamyltransferase 2 MeSH
- GTP-Binding Proteins MeSH
- Transglutaminases MeSH
The present study aims to report on the correlation between the degree of negativity of anti-endomysial antibodies and anti-tissue transglutaminase antibodies in the IgA and IgG classes with regard to histological grade, in 44 newly diagnosed children with celiac disease (CD). Samples with negative antibodies, but a positive histology from a 5-year program searching for CD in the pediatric population were collected. A total of 4247 biopsy samples were used in this study. We documented that certain pediatric patients are seronegative, while the disease is active and the incidence of CD is higher than expected in the pediatric population. This is an important finding, which demonstrates the lack of association between autoantibodies and lesions, and justifies the use of biopsies for an accurate CD diagnosis and the importance of revising the diagnostic criteria in a clinical, endoscopic and serological context. We recommend a more active search for incidences of the disease in the pediatric population. Serological markers are not the main method for the diagnosis of CD as they are considered to only have a supporting role clinically. Biopsies of the small intestine are always necessary for the diagnosis of CD in these patients.
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