Early Antibody Dynamics in a Prospective Cohort of Children At Risk of Celiac Disease.


Journal

The American journal of gastroenterology
ISSN: 1572-0241
Titre abrégé: Am J Gastroenterol
Pays: United States
ID NLM: 0421030

Informations de publication

Date de publication:
01 03 2023
Historique:
received: 25 09 2022
accepted: 10 01 2023
pmc-release: 01 03 2024
pubmed: 3 2 2023
medline: 7 3 2023
entrez: 2 2 2023
Statut: ppublish

Résumé

The purpose of this study was to identify possible serum biomarkers predicting celiac disease (CD) onset in children at risk. A subgroup from an ongoing, international prospective study of children at risk of CD was classified according to an early trajectory of deamidated gliadin peptides (DGPs) immunoglobulin (Ig) G and clinical outcomes (CD, potential CD, and CD autoimmunity). Thirty-eight of 325 children developed anti-tissue transglutaminase IgA antibody (anti-tTG IgA) seroconversion. Twenty-eight of 38 children (73.6%) showed an increase in anti-DGPs IgG before their first anti-tTG IgA seroconversion. Anti-DGPs IgG can represent an early preclinical biomarker predicting CD onset in children at risk.

Identifiants

pubmed: 36727859
doi: 10.14309/ajg.0000000000002192
pii: 00000434-202303000-00039
pmc: PMC9992331
mid: NIHMS1866458
doi:

Substances chimiques

Gliadin 9007-90-3
Immunoglobulin A 0
Autoantibodies 0
Immunoglobulin G 0
Biomarkers 0
Transglutaminases EC 2.3.2.13

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

574-577

Subventions

Organisme : NIDDK NIH HHS
ID : K23 DK122127
Pays : United States
Organisme : NIDDK NIH HHS
ID : L40 DK115176
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK104344
Pays : United States
Organisme : NIAID NIH HHS
ID : R56 AI156711
Pays : United States

Informations de copyright

Copyright © 2023 by The American College of Gastroenterology.

Références

Husby S, Koletzko S, Korponay-Szabó I, et al. European Society Paediatric Gastroenterology, Hepatology and Nutrition guidelines for diagnosing coeliac disease 2020. J Pediatr Gastroenterol Nutr 2020;70(1):141–56.
Hill ID, Fasano A, Guandalini S, et al. NASPGHAN clinical report on the diagnosis and treatment of gluten-related disorders. J Pediatr Gastroenterol Nutr 2016;63(1):156–65.
Liu E, Li M, Emery L, et al. Natural history of antibodies to deamidated gliadin peptides and transglutaminase in early childhood celiac disease. J Pediatr Gastroenterol Nutr 2007;45(3):293–300.
Barbato M, Maiella G, Di Camillo C, et al. The anti-deamidated gliadin peptide antibodies unmask celiac disease in small children with chronic diarrhoea. Dig Liver Dis 2011;43(6):465–9.
Gould MJ, Brill H, Marcon MA, et al. In screening for celiac disease, deamidated gliadin rarely predicts disease when tissue transglutaminase is normal. J Pediatr Gastroenterol Nutr 2019;68(1):20–5.
Khan MR, Silvester JA, Sparks B, et al. The utility of IgA-based serologic markers in diagnosing celiac disease in children 24 months of age or younger. J Pediatr 2020;224:158–61.e2.
Leonard MM, Valitutti F, Karathia H, et al. Microbiome signatures of progression toward celiac disease onset in at-risk children in a longitudinal prospective cohort study. Proc Natl Acad Sci USA 2021;118(29):118.
van de Wal Y, Kooy Y, van Veelen P, et al. Cutting edge: Selective deamidation by tissue transglutaminase strongly enhances gliadin-specific T cell reactivity. J Immunol 1998;161(4):1585–8.
Catassi GN, Pulvirenti A, Monachesi C, et al. Diagnostic accuracy of IgA anti-transglutaminase and IgG anti-deamidated gliadin for diagnosis of celiac disease in children under two years of age: A systematic review and meta-analysis. Nutrients 2021;14(1):7.
Segerstad EMHA, Liu X, Uusitalo U, et al. Sources of dietary gluten in the first two years of life and associations with celiac disease autoimmunity and celiac disease in Swedish genetically predisposed children: TEDDY study. Am J Clin Nutr 2022;116(2):394–403.
Auricchio R, Mandile R, Del Vecchio MR, et al. Progression of celiac disease in children with antibodies against tissue transglutaminase and normal duodenal architecture. Gastroenterology 2019;157(2):413–20.e3.
Catassi GN, Vallorani M, Cerioni F, et al. A negative fallout of COVID-19 lockdown in Italy: Life-threatening delay in the diagnosis of celiac disease. Dig Liver Dis 2020;52(10):1092–3.

Auteurs

Francesco Valitutti (F)

Pediatric Unit, "San Giovanni di Dio e Ruggi d'Aragona" University Hospital, Salerno, Italy.
European Biomedical Research Institute of Salerno, Salerno, Italy.

Maureen M Leonard (MM)

Division of Pediatric Gastroenterology and Nutrition, MassGeneral Hospital for Children, Harvard Medical School, Boston, Massachusetts, USA.
Celiac Research Program, Harvard Medical School, Boston, Massachusetts, USA.

Victoria Kenyon (V)

Division of Pediatric Gastroenterology and Nutrition, MassGeneral Hospital for Children, Harvard Medical School, Boston, Massachusetts, USA.
Celiac Research Program, Harvard Medical School, Boston, Massachusetts, USA.

Monica Montuori (M)

Pediatric Gastroenterology Unit, Policlinico Umberto I, Sapienza University of Rome, Rome, Italy.

Pasqua Piemontese (P)

NICU, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.

Ruggiero Francavilla (R)

Pediatric Unit "Bruno Trambusti," Osp Pediatrico Giovanni XXIII, University of Bari, Bari, Italy.

Basilio Malamisura (B)

Celiac Disease Referral Center, "San Giovanni di Dio e Ruggi d'Aragona" University Hospital, Pole of Cava de' Tirreni, Salerno, Italy.

Lorenzo Norsa (L)

Pediatric Hepatology Gastroenterology and Transplant Unit, Ospedale Papa Giovanni XXIII Bergamo, Bergamo, Italy.

Angela Calvi (A)

Pediatrics, IRCCS Ospedale Giannina Gaslini, Genova, Italy.

Maria Elena Lionetti (ME)

Pediatrics, Univ. Politec. delle Marche, Ancona, Italy.

Mariella Baldassarre (M)

NICU, University of Bari, Bari, Italy.

Chiara Maria Trovato (CM)

Celiac Disease Referral Center, Bambino Gesù Hospital, Rome, Italy.

Michela Perrone (M)

NICU, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.

Tiziana Passaro (T)

Celiac Disease Referral Center, "San Giovanni di Dio e Ruggi d'Aragona" University Hospital, Pole of Cava de' Tirreni, Salerno, Italy.

Naire Sansotta (N)

Pediatric Hepatology Gastroenterology and Transplant Unit, Ospedale Papa Giovanni XXIII Bergamo, Bergamo, Italy.

Marco Crocco (M)

Pediatrics, IRCCS Ospedale Giannina Gaslini, Genova, Italy.

Annalisa Morelli (A)

Pediatric Training Program, University of Salerno School of Medicine, Salerno, Italy.

Lidia Celeste Raguseo (LC)

Pediatric Unit "Bruno Trambusti," Osp Pediatrico Giovanni XXIII, University of Bari, Bari, Italy.

Federica Malerba (F)

Pediatrics, IRCCS Ospedale Giannina Gaslini, Genova, Italy.

Luca Elli (L)

Celiac Disease Referral Center, Ospedale Maggiore Policlinico, Milan, Italy.

Fernanda Cristofori (F)

Pediatric Unit "Bruno Trambusti," Osp Pediatrico Giovanni XXIII, University of Bari, Bari, Italy.

Carlo Catassi (C)

Pediatrics, Univ. Politec. delle Marche, Ancona, Italy.

Alessio Fasano (A)

European Biomedical Research Institute of Salerno, Salerno, Italy.
Division of Pediatric Gastroenterology and Nutrition, MassGeneral Hospital for Children, Harvard Medical School, Boston, Massachusetts, USA.
Celiac Research Program, Harvard Medical School, Boston, Massachusetts, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH