Role of age in dynamics of autoantibodies in pediatric Celiac disease

Abstract Background Celiac disease (CD) is characterized by elevated serum titers of autoantibodies IgA anti-tissue transglutaminase 2 (TGA-IgA) and IgA anti-endomysial (EMA), with small bowel mucosa atrophy. We evaluated age differences between CD children exhibiting variable antibody titers at dia...

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Main Authors: Chiara Maria Trovato, Monica Montuori, Beatrice Leter, Ilaria Laudadio, Giusy Russo, Salvatore Oliva
Format: Article
Language:English
Published: BMC 2023-03-01
Series:Italian Journal of Pediatrics
Subjects:
Online Access:https://doi.org/10.1186/s13052-023-01435-6
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author Chiara Maria Trovato
Monica Montuori
Beatrice Leter
Ilaria Laudadio
Giusy Russo
Salvatore Oliva
author_facet Chiara Maria Trovato
Monica Montuori
Beatrice Leter
Ilaria Laudadio
Giusy Russo
Salvatore Oliva
author_sort Chiara Maria Trovato
collection DOAJ
description Abstract Background Celiac disease (CD) is characterized by elevated serum titers of autoantibodies IgA anti-tissue transglutaminase 2 (TGA-IgA) and IgA anti-endomysial (EMA), with small bowel mucosa atrophy. We evaluated age differences between CD children exhibiting variable antibody titers at diagnosis. Methods CD children diagnosed between January 2014 and June 2019, according to 2012 ESPGHAN guidelines were studied. All had EMA and TGA-IgA measurements, while a proportion of them underwent esophagogastroduodenoscopy (EGD). Patients were grouped based on serum TGA-IgA titers normalized to the upper limit of normal (ULN) and differences in median age (years) assessed by analysis of variance (ANOVA) and creation of orthogonal contrasts. Results CD was diagnosed in 295 subjects (median age: 4.4 [IQR: 2.60–8.52]) with a biopsy sparing protocol (high titer: ≥ 10xULN) and in 204 by EGD biopsy. Of the latter, 142 (median age: 8.5 [IQR: 5.81–11.06]) and 62 (median age: 9.5 [IQR: 6.26–12.76]) had a low (< 5xULN) and a moderate (≥ 5 < 10xULN) TGA-IgA titer, respectively. Potential CD was diagnosed in 20 patients (median age: 3.6 [IQR: 2.47–6.91]). The median age was significantly lower in the no-biopsy group (ANOVA: F(3, 516) = 25.98, p < .001) than in low- and moderate titer groups (p < 0.0001), while there was no statistical difference between biopsy-sparing and potential CD groups. Conclusion CD patients with greatly elevated antibody titers (≥ 10xULN) were diagnosed at an earlier age than those with lower titers. This may indicate that an increase in TGA-IgA is independent of age and suggests a polarization of autoimmunity in younger individuals with higher serum antibody levels.
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spelling doaj.art-982c5d7bcc664c99823b2d6d787ee0bd2023-03-26T11:15:04ZengBMCItalian Journal of Pediatrics1824-72882023-03-014911610.1186/s13052-023-01435-6Role of age in dynamics of autoantibodies in pediatric Celiac diseaseChiara Maria Trovato0Monica Montuori1Beatrice Leter2Ilaria Laudadio3Giusy Russo4Salvatore Oliva5Gastroenterology and Nutritional Rehabilitation Unit, I.R.C.C.S. Bambino Gesù Children’s HospitalPediatric Gastroenterology and Liver Unit, Maternal and Child Health Department, Sapienza University of RomeDepartment of Molecular Medicine, Sapienza University of RomeDepartment of Molecular Medicine, Sapienza University of RomePediatric Gastroenterology and Liver Unit, Maternal and Child Health Department, Sapienza University of RomePediatric Gastroenterology and Liver Unit, Maternal and Child Health Department, Sapienza University of RomeAbstract Background Celiac disease (CD) is characterized by elevated serum titers of autoantibodies IgA anti-tissue transglutaminase 2 (TGA-IgA) and IgA anti-endomysial (EMA), with small bowel mucosa atrophy. We evaluated age differences between CD children exhibiting variable antibody titers at diagnosis. Methods CD children diagnosed between January 2014 and June 2019, according to 2012 ESPGHAN guidelines were studied. All had EMA and TGA-IgA measurements, while a proportion of them underwent esophagogastroduodenoscopy (EGD). Patients were grouped based on serum TGA-IgA titers normalized to the upper limit of normal (ULN) and differences in median age (years) assessed by analysis of variance (ANOVA) and creation of orthogonal contrasts. Results CD was diagnosed in 295 subjects (median age: 4.4 [IQR: 2.60–8.52]) with a biopsy sparing protocol (high titer: ≥ 10xULN) and in 204 by EGD biopsy. Of the latter, 142 (median age: 8.5 [IQR: 5.81–11.06]) and 62 (median age: 9.5 [IQR: 6.26–12.76]) had a low (< 5xULN) and a moderate (≥ 5 < 10xULN) TGA-IgA titer, respectively. Potential CD was diagnosed in 20 patients (median age: 3.6 [IQR: 2.47–6.91]). The median age was significantly lower in the no-biopsy group (ANOVA: F(3, 516) = 25.98, p < .001) than in low- and moderate titer groups (p < 0.0001), while there was no statistical difference between biopsy-sparing and potential CD groups. Conclusion CD patients with greatly elevated antibody titers (≥ 10xULN) were diagnosed at an earlier age than those with lower titers. This may indicate that an increase in TGA-IgA is independent of age and suggests a polarization of autoimmunity in younger individuals with higher serum antibody levels.https://doi.org/10.1186/s13052-023-01435-6Anti-tissue transglutaminaseAnti-endomysialCeliac diseaseChildren
spellingShingle Chiara Maria Trovato
Monica Montuori
Beatrice Leter
Ilaria Laudadio
Giusy Russo
Salvatore Oliva
Role of age in dynamics of autoantibodies in pediatric Celiac disease
Italian Journal of Pediatrics
Anti-tissue transglutaminase
Anti-endomysial
Celiac disease
Children
title Role of age in dynamics of autoantibodies in pediatric Celiac disease
title_full Role of age in dynamics of autoantibodies in pediatric Celiac disease
title_fullStr Role of age in dynamics of autoantibodies in pediatric Celiac disease
title_full_unstemmed Role of age in dynamics of autoantibodies in pediatric Celiac disease
title_short Role of age in dynamics of autoantibodies in pediatric Celiac disease
title_sort role of age in dynamics of autoantibodies in pediatric celiac disease
topic Anti-tissue transglutaminase
Anti-endomysial
Celiac disease
Children
url https://doi.org/10.1186/s13052-023-01435-6
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