Endomysial antibodies predict celiac disease irrespective of the titers or clinical presentation |
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Authors: | Kurppa Kalle Räsänen Tiia Collin Pekka Iltanen Sari Huhtala Heini Ashorn Merja Saavalainen Päivi Haimila Katri Partanen Jukka Mäki Markku Kaukinen Katri |
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Affiliation: | Pediatric Research Centre, University of Tampere and Tampere University Hospital, Fin-33014, Tampere, Finland. |
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Abstract: | AIM: To investigate the association between serum antibody levels and a subsequent celiac disease diagnosis in a large series of children and adults.METHODS: Besides subjects with classical gastrointestinal presentation of celiac disease, the study cohort included a substantial number of individuals with extraintestinal symptoms and those found by screening in at-risk groups. Altogether 405 patients underwent clinical, serological and histological evaluations. After collection of data, the antibody values were further graded as low [endomysial (EmA) 1:5-200, transglutaminase 2 antibodies (TG2-ab) 5.0-30.0 U/L] and high (EmA 1: ≥ 500, TG2-ab ≥ 30.0 U/L), and the serological results were compared with the small intestinal mucosal histology and clinical presentation.RESULTS: In total, 79% of the subjects with low and 94% of those with high serum EmA titers showed small-bowel mucosal villous atrophy. Furthermore, 96% of the 47 EmA positive subjects who had normal mucosal villi and remained on follow-up either subsequently developed mucosal atrophy while on a gluten-containing diet, or responded positively to a gluten-free diet.CONCLUSION: Irrespective of the initial serum titers or clinical presentation, EmA positivity as such is a very strong predictor of a subsequent celiac disease diagnosis. |
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Keywords: | Celiac disease Diagnosis Endomysial antibodies Transglutaminase 2 antibodies Clinical presentations |
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