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The age-specific microbiome of children with milk, egg, and peanut allergy.
Ponda, Punita; Cerise, Jane E; Navetta-Modrov, Brianne; Kiehm, Jamie; Covelli, Grace M; Weiss, Jared; Lee, Annette T.
Afiliação
  • Ponda P; Northwell, New Hyde Park, New York; Division of Allergy and Immunology, Cohen Children's Medical Center, New Hyde Park, New York. Electronic address: pponda@northwell.edu.
  • Cerise JE; Biostatistics Unit, Office of Academic Affairs, Northwell Health, New Hyde Park, New York.
  • Navetta-Modrov B; Department of Medicine, Stony Brook University School of Medicine, Stony Brook, New York.
  • Kiehm J; Los Angeles County Department of Health Services, Los Angeles, California.
  • Covelli GM; Walter Reed National Military Medical Center, Bethesda, Maryland.
  • Weiss J; Department of Psychiatry, New York University School of Medicine, New York, New York.
  • Lee AT; Northwell, New Hyde Park, New York; Institute of Molecular Medicine, Feinstein Institutes for Medical Research, Northwell Health, Manhasset, New York.
Ann Allergy Asthma Immunol ; 133(2): 203-210.e6, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38697287
ABSTRACT

BACKGROUND:

Immune regulation by gut microbiota is affected by dysbiosis and may precede food allergy onset. Prior studies lacked comparisons stratified by age and clinical phenotype.

OBJECTIVE:

To assess the microbiome of children with food allergy (<3 years, 3-18 years) compared with similar aged children without food allergy.

METHODS:

A real-world prospective cross-sectional study performed from 2014 to 2019 recruited children highly likely to have milk, egg, or peanut allergy defined by history and serum IgE or confirmed by food challenge. 16S ribosomal RNA sequencing identified stool microbial DNA. Alpha and beta diversity was compared between groups with food allergy and healthy controls stratified by age. Differential abundance for non a priori taxa was accepted at absolute fold-change greater than 2 and q value less than 0.05.

RESULTS:

A total of 70 patients were included (56 with food allergy and 14 healthy controls). Groups were not significantly different in age, gender at birth, race, mode of delivery, breastfeeding duration, or antibiotic exposure. Younger children with food allergy had similar alpha diversity compared with controls. Beta diversity was significantly different by age (P = .001). There was differential abundance of several a priori (P < .05) taxa (including Clostridia) only in younger children. Both a priori (including Coprococcus and Clostridia) and non a priori (q < 0.05) Acidobacteria_Gp15, Aestuariispira, Tindallia, and Desulfitispora were significant in older children with food allergy, especially with peanut allergy.

CONCLUSION:

Dysbiosis associates with food allergy, most prominent in older children with peanut allergy. Younger children with and without food allergy have fewer differences in gut microbiota. This correlates with clinical observations of persistence of peanut allergy and improved efficacy and safety of oral immunotherapy in younger children. Age younger than 3 years should be considered when initiating therapeutic interventions.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipersensibilidade a Leite / Hipersensibilidade a Ovo / Hipersensibilidade a Amendoim / Microbioma Gastrointestinal Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipersensibilidade a Leite / Hipersensibilidade a Ovo / Hipersensibilidade a Amendoim / Microbioma Gastrointestinal Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article