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Untargeted, High-Resolution Metabolomics in Pediatric Eosinophilic Esophagitis.
Sinclair, Elizabeth M; Cohen, Catherine C; Tran, ViLinh; Jones, Dean P; Alvarez, Jessica A; Kamaleswaran, Rishikesan; Rad, Milad Ghiasi; Kruszewski, Patrice G; Vos, Miriam B.
Affiliation
  • Sinclair EM; From the Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA.
  • Cohen CC; the Pediatric Gastroenterology, Hepatology & Nutrition, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, PA.
  • Tran V; the Department of Pediatrics, University of Colorado Denver Anschutz Medical Campus, Aurora, CO.
  • Jones DP; the Department of Medicine, Emory University School of Medicine, Atlanta, GA.
  • Alvarez JA; the Department of Medicine, Emory University School of Medicine, Atlanta, GA.
  • Kamaleswaran R; the Department of Medicine, Emory University School of Medicine, Atlanta, GA.
  • Rad MG; the Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Kruszewski PG; the Department of Biomedical Informatics, Emory University School of Medicine, Atlanta, GA.
  • Vos MB; the Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA.
J Pediatr Gastroenterol Nutr ; 76(3): 355-363, 2023 03 01.
Article de En | MEDLINE | ID: mdl-36728821
BACKGROUND/OBJECTIVES: Eosinophilic esophagitis (EoE) is an inflammatory disease of unclear etiology. The aim of this study was to use untargeted plasma metabolomics to identify metabolic pathway alterations associated with EoE to better understand the pathophysiology. METHODS: This prospective, case-control study included 72 children, aged 1-17 years, undergoing clinically indicated upper endoscopy (14 diagnosed with EoE and 58 controls). Fasting plasma samples were analyzed for metabolomics by high-resolution dual-chromatography mass spectrometry. Analysis was performed on sex-matched groups at a 2:1 ratio. Significant differences among the plasma metabolite features between children with and without EoE were determined using multivariate regression analysis and were annotated with a network-based algorithm. Subsequent pathway enrichment analysis was performed. RESULTS: Patients with EoE had a higher proportion of atopic disease (85.7% vs 50%, P = 0.019) and any allergies (100% vs 57.1%, P = 0.0005). Analysis of the dual chromatography features resulted in a total of 918 metabolites that differentiated EoE and controls. Glycerophospholipid metabolism was significantly enriched with the greatest number of differentiating metabolites and overall pathway enrichment ( P < 0.01). Multiple amino and fatty acid pathways including linoleic acid were also enriched, as well as pyridoxine metabolism ( P < 0.01). CONCLUSIONS: In this pilot study, we found differences in metabolites involved in glycerophospholipid and inflammation pathways in pediatric patients with EoE using untargeted metabolomics, as well as overlap with amino acid metabolome alterations found in atopic disease.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Oesophagite à éosinophiles Type d'étude: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Child / Humans Langue: En Journal: J Pediatr Gastroenterol Nutr Année: 2023 Type de document: Article Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Oesophagite à éosinophiles Type d'étude: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Child / Humans Langue: En Journal: J Pediatr Gastroenterol Nutr Année: 2023 Type de document: Article Pays de publication: États-Unis d'Amérique