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Progression of pediatric celiac disease from potential celiac disease to celiac disease: a retrospective cohort study

BACKGROUND: A subset of patients with serology suggesting celiac disease have an initially negative biopsy but subsequently develop histopathologic celiac disease. Here we characterize patients with potential celiac disease who progress to celiac disease. METHODS: We performed a retrospective analys...

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Autores principales: Sakhuja, Shruti, Holtz, Lori R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006356/
https://www.ncbi.nlm.nih.gov/pubmed/33781221
http://dx.doi.org/10.1186/s12887-021-02625-z
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author Sakhuja, Shruti
Holtz, Lori R.
author_facet Sakhuja, Shruti
Holtz, Lori R.
author_sort Sakhuja, Shruti
collection PubMed
description BACKGROUND: A subset of patients with serology suggesting celiac disease have an initially negative biopsy but subsequently develop histopathologic celiac disease. Here we characterize patients with potential celiac disease who progress to celiac disease. METHODS: We performed a retrospective analysis of children (0–18 years of age) with biopsy-confirmed celiac disease seen at St. Louis Children’s Hospital between 2013 and 2018. RESULTS: Three hundred sixteen of 327 (96%) children with biopsy-confirmed celiac disease were diagnosed on initial biopsy. The 11 children with potential celiac disease who progressed to celiac disease had lower anti-tissue transglutaminase (anti-TTG IgA) concentrations (2.4 (1.6–5) X upper limit of normal (ULN) vs. 6.41 (3.4–10.5) X ULN) at time of first biopsy. Their median anti-TTG IgA concentrations rose from 2.4 (1.6–5) X ULN to 3.6 (3.1–9.2) X ULN between biopsies. CONCLUSIONS: Four percent of biopsy confirmed celiac patients initially had a negative biopsy, but later developed histopathologic celiac disease. This is likely an underestimate as no surveillance algorithm was in place. We recommend repeat assessment in children whose serology suggests celiac disease despite normal small bowel biopsy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-021-02625-z.
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spelling pubmed-80063562021-03-30 Progression of pediatric celiac disease from potential celiac disease to celiac disease: a retrospective cohort study Sakhuja, Shruti Holtz, Lori R. BMC Pediatr Research Article BACKGROUND: A subset of patients with serology suggesting celiac disease have an initially negative biopsy but subsequently develop histopathologic celiac disease. Here we characterize patients with potential celiac disease who progress to celiac disease. METHODS: We performed a retrospective analysis of children (0–18 years of age) with biopsy-confirmed celiac disease seen at St. Louis Children’s Hospital between 2013 and 2018. RESULTS: Three hundred sixteen of 327 (96%) children with biopsy-confirmed celiac disease were diagnosed on initial biopsy. The 11 children with potential celiac disease who progressed to celiac disease had lower anti-tissue transglutaminase (anti-TTG IgA) concentrations (2.4 (1.6–5) X upper limit of normal (ULN) vs. 6.41 (3.4–10.5) X ULN) at time of first biopsy. Their median anti-TTG IgA concentrations rose from 2.4 (1.6–5) X ULN to 3.6 (3.1–9.2) X ULN between biopsies. CONCLUSIONS: Four percent of biopsy confirmed celiac patients initially had a negative biopsy, but later developed histopathologic celiac disease. This is likely an underestimate as no surveillance algorithm was in place. We recommend repeat assessment in children whose serology suggests celiac disease despite normal small bowel biopsy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-021-02625-z. BioMed Central 2021-03-29 /pmc/articles/PMC8006356/ /pubmed/33781221 http://dx.doi.org/10.1186/s12887-021-02625-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Sakhuja, Shruti
Holtz, Lori R.
Progression of pediatric celiac disease from potential celiac disease to celiac disease: a retrospective cohort study
title Progression of pediatric celiac disease from potential celiac disease to celiac disease: a retrospective cohort study
title_full Progression of pediatric celiac disease from potential celiac disease to celiac disease: a retrospective cohort study
title_fullStr Progression of pediatric celiac disease from potential celiac disease to celiac disease: a retrospective cohort study
title_full_unstemmed Progression of pediatric celiac disease from potential celiac disease to celiac disease: a retrospective cohort study
title_short Progression of pediatric celiac disease from potential celiac disease to celiac disease: a retrospective cohort study
title_sort progression of pediatric celiac disease from potential celiac disease to celiac disease: a retrospective cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006356/
https://www.ncbi.nlm.nih.gov/pubmed/33781221
http://dx.doi.org/10.1186/s12887-021-02625-z
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