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Influence of Age and Type 1 Diabetes Mellitus on Serological Test for Celiac Disease in Children

PURPOSE: Serological tests of tissue transglutaminase (TTG) and deamidated gliadin (DGP) antibodies for celiac disease diagnosis show conflicting correlation with histology in young children and in type 1 diabetes mellitus (T1DM). Tests' ability to predict histology and cutoff values based on a...

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Autores principales: Maheshwari, Anshu, He, Zhaoping, Weidner, Melissa Nicole, Lin, Patrick, Bober, Ryan, Del Rosario, Fernando J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007846/
https://www.ncbi.nlm.nih.gov/pubmed/33833977
http://dx.doi.org/10.5223/pghn.2021.24.2.218
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author Maheshwari, Anshu
He, Zhaoping
Weidner, Melissa Nicole
Lin, Patrick
Bober, Ryan
Del Rosario, Fernando J.
author_facet Maheshwari, Anshu
He, Zhaoping
Weidner, Melissa Nicole
Lin, Patrick
Bober, Ryan
Del Rosario, Fernando J.
author_sort Maheshwari, Anshu
collection PubMed
description PURPOSE: Serological tests of tissue transglutaminase (TTG) and deamidated gliadin (DGP) antibodies for celiac disease diagnosis show conflicting correlation with histology in young children and in type 1 diabetes mellitus (T1DM). Tests' ability to predict histology and cutoff values based on age and T1DM was evaluated. METHODS: A retrospective study of children who had celiac serological tests between 6/1/2002 and 12/31/2014 at a pediatric hospital. RESULTS: TTG IgA displayed similar results in predicting histology between <4.0 and ≥4.0 years age groups with sensitivity 98% and 93%, and specificity 88% and 86%, respectively. In children <4.0 years old, sensitivity for DGP antibodies was 100% and specificity 94%; in ≥4.0 years age groups, sensitivity was 60%, 88% for DGP IgA and IgG and specificity 95%, 96%, respectively. TTG IgA had low specificity in patients with T1DM compared with non-T1DM, 42% vs. 91%. Positive TTG IgA with normal histology was associated with higher T1DM prevalence at 36% compared with negative tests at 4%. Finally, the TTG IgA cutoff value was higher in T1DM at 36 vs. 16.3 units in non-T1DM. DGP IgG cutoff showed similar values between age groups; TTG IgA and DGP IgA cutoffs were lower in <4.0 years at 8.3 and 11.9 units than ≥4.0 years at 23.4 and 19.9, respectively. CONCLUSION: TTG IgA is sufficient for the <4.0 years age group and DGP antibodies had no advantage over TTG IgA in older children. The cutoff value to determine a positive TTG IgA should be higher for children with T1DM.
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spelling pubmed-80078462021-04-07 Influence of Age and Type 1 Diabetes Mellitus on Serological Test for Celiac Disease in Children Maheshwari, Anshu He, Zhaoping Weidner, Melissa Nicole Lin, Patrick Bober, Ryan Del Rosario, Fernando J. Pediatr Gastroenterol Hepatol Nutr Original Article PURPOSE: Serological tests of tissue transglutaminase (TTG) and deamidated gliadin (DGP) antibodies for celiac disease diagnosis show conflicting correlation with histology in young children and in type 1 diabetes mellitus (T1DM). Tests' ability to predict histology and cutoff values based on age and T1DM was evaluated. METHODS: A retrospective study of children who had celiac serological tests between 6/1/2002 and 12/31/2014 at a pediatric hospital. RESULTS: TTG IgA displayed similar results in predicting histology between <4.0 and ≥4.0 years age groups with sensitivity 98% and 93%, and specificity 88% and 86%, respectively. In children <4.0 years old, sensitivity for DGP antibodies was 100% and specificity 94%; in ≥4.0 years age groups, sensitivity was 60%, 88% for DGP IgA and IgG and specificity 95%, 96%, respectively. TTG IgA had low specificity in patients with T1DM compared with non-T1DM, 42% vs. 91%. Positive TTG IgA with normal histology was associated with higher T1DM prevalence at 36% compared with negative tests at 4%. Finally, the TTG IgA cutoff value was higher in T1DM at 36 vs. 16.3 units in non-T1DM. DGP IgG cutoff showed similar values between age groups; TTG IgA and DGP IgA cutoffs were lower in <4.0 years at 8.3 and 11.9 units than ≥4.0 years at 23.4 and 19.9, respectively. CONCLUSION: TTG IgA is sufficient for the <4.0 years age group and DGP antibodies had no advantage over TTG IgA in older children. The cutoff value to determine a positive TTG IgA should be higher for children with T1DM. The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2021-03 2021-03-04 /pmc/articles/PMC8007846/ /pubmed/33833977 http://dx.doi.org/10.5223/pghn.2021.24.2.218 Text en Copyright © 2021 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition https://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Maheshwari, Anshu
He, Zhaoping
Weidner, Melissa Nicole
Lin, Patrick
Bober, Ryan
Del Rosario, Fernando J.
Influence of Age and Type 1 Diabetes Mellitus on Serological Test for Celiac Disease in Children
title Influence of Age and Type 1 Diabetes Mellitus on Serological Test for Celiac Disease in Children
title_full Influence of Age and Type 1 Diabetes Mellitus on Serological Test for Celiac Disease in Children
title_fullStr Influence of Age and Type 1 Diabetes Mellitus on Serological Test for Celiac Disease in Children
title_full_unstemmed Influence of Age and Type 1 Diabetes Mellitus on Serological Test for Celiac Disease in Children
title_short Influence of Age and Type 1 Diabetes Mellitus on Serological Test for Celiac Disease in Children
title_sort influence of age and type 1 diabetes mellitus on serological test for celiac disease in children
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007846/
https://www.ncbi.nlm.nih.gov/pubmed/33833977
http://dx.doi.org/10.5223/pghn.2021.24.2.218
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