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Evaluation of Celiac Disease by Minimally Invasive Biomarkers in a Spanish Pediatric Population
Background: The diagnosis of celiac disease (CD) has been substantially improved with the availability of highly sensitive CD-specific IgA-TG2, Ig-GDP, and IgA-EMA. The European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) published (2012) and updated (2020) diagnostic...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100138/ https://www.ncbi.nlm.nih.gov/pubmed/35564413 http://dx.doi.org/10.3390/ijerph19095020 |
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author | Cabo del Riego, Julia María Núñez Iglesias, María Jesús García-Plata González, Carmen Paz Carreira, José Álvarez Fernández, Tamara Dorado Díaz, Ana Villar Mallo, Noa Penedo Pita, Manuel Novío Mallón, Silvia Máiz Suárez, Lola Freire-Garabal Núñez, Manuel |
author_facet | Cabo del Riego, Julia María Núñez Iglesias, María Jesús García-Plata González, Carmen Paz Carreira, José Álvarez Fernández, Tamara Dorado Díaz, Ana Villar Mallo, Noa Penedo Pita, Manuel Novío Mallón, Silvia Máiz Suárez, Lola Freire-Garabal Núñez, Manuel |
author_sort | Cabo del Riego, Julia María |
collection | PubMed |
description | Background: The diagnosis of celiac disease (CD) has been substantially improved with the availability of highly sensitive CD-specific IgA-TG2, Ig-GDP, and IgA-EMA. The European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) published (2012) and updated (2020) diagnostic criteria for CD in order to simplify CD diagnosis and to avoid biopsies in selected patients. Methods: A prospective study including 5641 pediatric patients (0–16 years old) from January 2012 to January 2019 was performed. CD diagnosis was made according to the ESPGHAN algorithm. The objective of this study was to evaluate the utility of biomarkers and the relationship between TGA-IgA and EMA titers. Results: CD diagnoses were confirmed in 113 patients, 110 were IgA-TG2-positive and 3 (2.7%) had IgA deficiency. The diagnosis was made by serologic tests in 95 (84.1%) patients. Only 18 (15.9%) patients underwent intestinal biopsy. We obtained 100% concordance between IgA-EMA and positive results for IgA-TG2 ≥ 10 ULN with IgA-EMA antibody titer ≥ 1:80. Conclusions: This study provides evidence of a positive correlation between IgA-TG2 antibody serum levels and IgA-EMA. The diagnosis could be guaranteed with strict application of IgA-TG2 values ≥ 10 ULN (confirmed by subsequent testing) plus the serological response to the gluten-free diet (GFD). |
format | Online Article Text |
id | pubmed-9100138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91001382022-05-14 Evaluation of Celiac Disease by Minimally Invasive Biomarkers in a Spanish Pediatric Population Cabo del Riego, Julia María Núñez Iglesias, María Jesús García-Plata González, Carmen Paz Carreira, José Álvarez Fernández, Tamara Dorado Díaz, Ana Villar Mallo, Noa Penedo Pita, Manuel Novío Mallón, Silvia Máiz Suárez, Lola Freire-Garabal Núñez, Manuel Int J Environ Res Public Health Article Background: The diagnosis of celiac disease (CD) has been substantially improved with the availability of highly sensitive CD-specific IgA-TG2, Ig-GDP, and IgA-EMA. The European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) published (2012) and updated (2020) diagnostic criteria for CD in order to simplify CD diagnosis and to avoid biopsies in selected patients. Methods: A prospective study including 5641 pediatric patients (0–16 years old) from January 2012 to January 2019 was performed. CD diagnosis was made according to the ESPGHAN algorithm. The objective of this study was to evaluate the utility of biomarkers and the relationship between TGA-IgA and EMA titers. Results: CD diagnoses were confirmed in 113 patients, 110 were IgA-TG2-positive and 3 (2.7%) had IgA deficiency. The diagnosis was made by serologic tests in 95 (84.1%) patients. Only 18 (15.9%) patients underwent intestinal biopsy. We obtained 100% concordance between IgA-EMA and positive results for IgA-TG2 ≥ 10 ULN with IgA-EMA antibody titer ≥ 1:80. Conclusions: This study provides evidence of a positive correlation between IgA-TG2 antibody serum levels and IgA-EMA. The diagnosis could be guaranteed with strict application of IgA-TG2 values ≥ 10 ULN (confirmed by subsequent testing) plus the serological response to the gluten-free diet (GFD). MDPI 2022-04-20 /pmc/articles/PMC9100138/ /pubmed/35564413 http://dx.doi.org/10.3390/ijerph19095020 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cabo del Riego, Julia María Núñez Iglesias, María Jesús García-Plata González, Carmen Paz Carreira, José Álvarez Fernández, Tamara Dorado Díaz, Ana Villar Mallo, Noa Penedo Pita, Manuel Novío Mallón, Silvia Máiz Suárez, Lola Freire-Garabal Núñez, Manuel Evaluation of Celiac Disease by Minimally Invasive Biomarkers in a Spanish Pediatric Population |
title | Evaluation of Celiac Disease by Minimally Invasive Biomarkers in a Spanish Pediatric Population |
title_full | Evaluation of Celiac Disease by Minimally Invasive Biomarkers in a Spanish Pediatric Population |
title_fullStr | Evaluation of Celiac Disease by Minimally Invasive Biomarkers in a Spanish Pediatric Population |
title_full_unstemmed | Evaluation of Celiac Disease by Minimally Invasive Biomarkers in a Spanish Pediatric Population |
title_short | Evaluation of Celiac Disease by Minimally Invasive Biomarkers in a Spanish Pediatric Population |
title_sort | evaluation of celiac disease by minimally invasive biomarkers in a spanish pediatric population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100138/ https://www.ncbi.nlm.nih.gov/pubmed/35564413 http://dx.doi.org/10.3390/ijerph19095020 |
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