Comparing Gastrointestinal Endoscopy Findings in Children with Autism, Developmental Delay, or Typical Development.


Journal

The Journal of pediatrics
ISSN: 1097-6833
Titre abrégé: J Pediatr
Pays: United States
ID NLM: 0375410

Informations de publication

Date de publication:
Jan 2024
Historique:
received: 26 05 2023
revised: 11 08 2023
accepted: 13 09 2023
pubmed: 19 9 2023
medline: 19 9 2023
entrez: 18 9 2023
Statut: ppublish

Résumé

To compare endoscopic and histologic upper endoscopy (esophagogastroduodenoscopy [EGD]) findings in children with autism spectrum disorders (ASD) to age- and gender-matched controls with developmental delay (DD) or with typical development (TD). Retrospective, cross-sectional study of children undergoing EGD, identifying those diagnosed with ASD, and matching on age and gender to children with DD or TD in ratio of 1:1:2. Rates of EGD findings were compared between the 3 groups using χ² or Fisher exact test. Multivariable linear regression was performed to identify predictors of abnormal histology. A total of 2104 patients were included (526 ASD; 526 DD; 1052 TD). Children with ASD had higher rates of abnormal esophageal histology (ASD 38.4%; DD 33.4%; TD 30.4%, P = .008), particularly esophagitis. In multivariable modeling, ASD diagnosis was an independent predictor of abnormal esophageal histology (OR [95% CI] 1.38 [1.09, 1.76]) compared with TD. Stomach findings did not differ among the groups. In the duodenum, histologic abnormalities were observed with lower frequency in ASD (ASD 17.0%; DD 20.1%; TD 24.2%, P = .005). In multivariable analysis, ASD diagnosis was not a significant predictor (OR 0.78 [0.56, 1.09]) of abnormal duodenal histology. Children with ASD have higher rates of histologic esophagitis compared with age- and gender-matched DD and TD controls. ASD was a significant independent predictor of abnormal esophageal, but not, duodenal, histology. These results underscore the importance of EGD in children with ASD.

Identifiants

pubmed: 37722553
pii: S0022-3476(23)00600-5
doi: 10.1016/j.jpeds.2023.113737
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113737

Subventions

Organisme : NIDDK NIH HHS
ID : K23 DK119584
Pays : United States

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors have no conflicts of interest relevant to this article to disclose. Dr Hron is supported by National Institutes of Health (K23 DK133679) and NASPGHANAstra-Zeneca Research Award. Dr Silvester is supported by National Institutes of HealthK23 KD119584. The other authors received no external funding.

Auteurs

Sonia A Ballal (SA)

Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA. Electronic address: sonia.ballal@childrens.harvard.edu.

Saige Greenwell (S)

Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA.

Enju Liu (E)

Institutional Centers for Clinical and Translational Research, Boston Children's Hospital, Boston, MA.

Timothy Buie (T)

Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA.

Jocelyn Silvester (J)

Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA.

McKenzie Leier (M)

Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA.

Maura Filippelli (M)

Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA.

Athos Bousvaros (A)

Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA.

Bridget Hron (B)

Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA.

Classifications MeSH