Early infancy dysbiosis in food protein-induced enterocolitis syndrome: A prospective cohort study

Kuan Wen Su, Murat Cetinbas, Victoria M. Martin, Yamini V. Virkud, Hannah Seay, Renata Ndahayo, Rachael Rosow, Michael Elkort, Brinda Gupta, Eileen Kramer, Tetiana Pronchick, Susan Reuter, Ruslan I. Sadreyev, Jing Long Huang, Wayne G. Shreffler, Qian Yuan*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

7 Scopus citations

Abstract

Background: The microbiome associations of food protein-induced enterocolitis syndrome (FPIES) are understudied. We sought to prospectively define the clinical features of FPIES in a birth cohort, and investigate for the evidence of gut dysbiosis. Methods: We identified children diagnosed with FPIES in the Gastrointestinal Microbiome and Allergic Proctocolitis Study, a healthy infant cohort. Children were assessed and stools were collected at each well child visit. The clinical features of the children with FPIES were summarized. Stool microbiome was analyzed using 16S rRNA sequencing comparing children with and without FPIES. Results: Of the 874 children followed up for 3 years, 8 FPIES cases (4 male) were identified, yielding a cumulative incidence of 0.92%. The most common triggers were oat and rice (n = 3, each) followed by milk (n = 2). The children with FPIES were more likely to have family history of food allergy (50% vs. 15.9% among unaffected, p =.03). The average age of disease presentation was 6 months old. During the first 6 months of life, stool from children with FPIES contained significantly less Bifidobacterium adolescentis, but more pathobionts, including Bacteroides spp. (especially Bacteroides fragilis), Holdemania spp., Lachnobacterium spp., and Acinetobacter lwoffii. The short-chain fatty acid (SCFA)-producing Bifidobacterium shunt was expressed significantly less in the stool from FPIES children. Conclusions: In this cohort, the cumulative incidence over the 3-year study period was 0.92%. During the first 6 months of life, children with FPIES had evidence of dysbiosis and SCFA production pathway was expressed less in their stool, which may play an important role in the pathogenesis of FPIES.

Original languageEnglish
Pages (from-to)1595-1604
Number of pages10
JournalAllergy: European Journal of Allergy and Clinical Immunology
Volume78
Issue number6
DOIs
StatePublished - 06 2023

Bibliographical note

© 2023 European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.

Keywords

  • FPIES
  • Stool microbiome
  • birth cohort study
  • food allergy
  • food protein-induced enterocolitis syndrome
  • Allergens
  • Prospective Studies
  • Humans
  • RNA, Ribosomal, 16S/genetics
  • Infant
  • Male
  • Dysbiosis
  • Syndrome
  • Dietary Proteins/adverse effects
  • Child
  • Enterocolitis/epidemiology
  • Food Hypersensitivity/diagnosis

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