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Celiac Disease in Adult Patients: Specific Autoantibodies in the Diagnosis, Monitoring, and Screening
The increasing prevalence of celiac disease (CD), especially in adults, its atypical clinical presentation, and the strict, lifelong adherence to gluten-free diet (GFD) as the only option for healthy state create an imperative need for noninvasive methods that can effectively diagnose CD and monitor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996301/ https://www.ncbi.nlm.nih.gov/pubmed/24804083 http://dx.doi.org/10.1155/2014/623514 |
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author | Trigoni, Evagelia Tsirogianni, Alexandra Pipi, Elena Mantzaris, Gerassimos Papasteriades, Chryssa |
author_facet | Trigoni, Evagelia Tsirogianni, Alexandra Pipi, Elena Mantzaris, Gerassimos Papasteriades, Chryssa |
author_sort | Trigoni, Evagelia |
collection | PubMed |
description | The increasing prevalence of celiac disease (CD), especially in adults, its atypical clinical presentation, and the strict, lifelong adherence to gluten-free diet (GFD) as the only option for healthy state create an imperative need for noninvasive methods that can effectively diagnose CD and monitor GFD. Aim. Evaluation of anti-endomysium (EmA) and anti-tissue transglutaminase IgA (tTG-A) antibodies in CD diagnosis, GFD monitoring, and first degree relatives screening in CD adult patients. Methods. 70 newly diagnosed Greek adult patients, 70 controls, and 47 first degree relatives were tested for the presence of EmA and tTG-A. The CD patients were monitored during a 3-year period. Results. EmA predictive ability for CD diagnosis was slightly better compared to tTG-A (P = 0.043). EmA could assess compliance with GFD already from the beginning of the diet, while both EmA and tTG-A had an equal ability to discriminate between strictly and partially compliant patients after the first semester and so on. Screening of first degree relatives resulted in the identification of 2 undiagnosed CD cases. Conclusions. Both EmA and tTG-A are suitable markers in the CD diagnosis, in the screening of CD among first degree relatives, having also an equal performance in the long term monitoring. |
format | Online Article Text |
id | pubmed-3996301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-39963012014-05-06 Celiac Disease in Adult Patients: Specific Autoantibodies in the Diagnosis, Monitoring, and Screening Trigoni, Evagelia Tsirogianni, Alexandra Pipi, Elena Mantzaris, Gerassimos Papasteriades, Chryssa Autoimmune Dis Clinical Study The increasing prevalence of celiac disease (CD), especially in adults, its atypical clinical presentation, and the strict, lifelong adherence to gluten-free diet (GFD) as the only option for healthy state create an imperative need for noninvasive methods that can effectively diagnose CD and monitor GFD. Aim. Evaluation of anti-endomysium (EmA) and anti-tissue transglutaminase IgA (tTG-A) antibodies in CD diagnosis, GFD monitoring, and first degree relatives screening in CD adult patients. Methods. 70 newly diagnosed Greek adult patients, 70 controls, and 47 first degree relatives were tested for the presence of EmA and tTG-A. The CD patients were monitored during a 3-year period. Results. EmA predictive ability for CD diagnosis was slightly better compared to tTG-A (P = 0.043). EmA could assess compliance with GFD already from the beginning of the diet, while both EmA and tTG-A had an equal ability to discriminate between strictly and partially compliant patients after the first semester and so on. Screening of first degree relatives resulted in the identification of 2 undiagnosed CD cases. Conclusions. Both EmA and tTG-A are suitable markers in the CD diagnosis, in the screening of CD among first degree relatives, having also an equal performance in the long term monitoring. Hindawi Publishing Corporation 2014 2014-04-03 /pmc/articles/PMC3996301/ /pubmed/24804083 http://dx.doi.org/10.1155/2014/623514 Text en Copyright © 2014 Evagelia Trigoni et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Trigoni, Evagelia Tsirogianni, Alexandra Pipi, Elena Mantzaris, Gerassimos Papasteriades, Chryssa Celiac Disease in Adult Patients: Specific Autoantibodies in the Diagnosis, Monitoring, and Screening |
title | Celiac Disease in Adult Patients: Specific Autoantibodies in the Diagnosis, Monitoring, and Screening |
title_full | Celiac Disease in Adult Patients: Specific Autoantibodies in the Diagnosis, Monitoring, and Screening |
title_fullStr | Celiac Disease in Adult Patients: Specific Autoantibodies in the Diagnosis, Monitoring, and Screening |
title_full_unstemmed | Celiac Disease in Adult Patients: Specific Autoantibodies in the Diagnosis, Monitoring, and Screening |
title_short | Celiac Disease in Adult Patients: Specific Autoantibodies in the Diagnosis, Monitoring, and Screening |
title_sort | celiac disease in adult patients: specific autoantibodies in the diagnosis, monitoring, and screening |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996301/ https://www.ncbi.nlm.nih.gov/pubmed/24804083 http://dx.doi.org/10.1155/2014/623514 |
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