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Celiac Disease in Adult Patients: Specific Autoantibodies in the Diagnosis, Monitoring, and Screening
Author(s) -
Evagelia Trigoni,
Alexandra Tsirogianni,
Elena Pipi,
Gerassimos J. Mantzaris,
Chryssa Papasteriades
Publication year - 2014
Publication title -
autoimmune diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.681
H-Index - 32
eISSN - 2090-0422
pISSN - 2090-0430
DOI - 10.1155/2014/623514
Subject(s) - medicine , first degree relatives , tissue transglutaminase , gluten free , autoantibody , disease , gastroenterology , antibody , pediatrics , immunology , family history , biochemistry , biology , enzyme
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.

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