Sensitization to peanut, egg or pets is associated with skin barrier dysfunction in children with atopic dermatitis.


Journal

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology
ISSN: 1365-2222
Titre abrégé: Clin Exp Allergy
Pays: England
ID NLM: 8906443

Informations de publication

Date de publication:
05 2021
Historique:
revised: 21 02 2021
received: 08 10 2020
accepted: 24 02 2021
pubmed: 16 3 2021
medline: 3 2 2022
entrez: 15 3 2021
Statut: ppublish

Résumé

Children with atopic dermatitis (AD) are often sensitized to food and aeroallergens, but sensitization patterns have not been analysed with biologic measures of disease pathogenicity. We sought to define allergen sensitization grouping(s) using unbiased machine learning and determine their associations with skin filaggrin (FLG) and transepidermal water loss (TEWL) (assesses skin barrier integrity), S100A8 and S100A9 expression (assesses skin inflammation) and AD severity. We studied 400 children with AD in the Mechanisms of Progression from Atopic Dermatitis to Asthma in Children (MPAACH) cohort to identify groupings of food and aeroallergen sensitizations. MPAACH is a paediatric AD cohort, aged 1-2, recruited through hospital/community settings between 2016 and 2018. We analysed these groupings' associations with AD biomarkers: skin FLG, S100A8 and S100A9 expression, total IgE, TEWL and AD severity. An unbiased machine learning approach revealed five allergen clusters. The most common cluster (N = 131), SPT In this largely clinic-based cohort of young children with AD, allergic sensitization to peanut, egg, cat or dog was associated with more severe disease and skin barrier function but not markers of cutaneous inflammation. These data need replicating in a population-based cohort but may have important implications for understanding the interaction between AD and allergic sensitization.

Sections du résumé

BACKGROUND
Children with atopic dermatitis (AD) are often sensitized to food and aeroallergens, but sensitization patterns have not been analysed with biologic measures of disease pathogenicity.
OBJECTIVE
We sought to define allergen sensitization grouping(s) using unbiased machine learning and determine their associations with skin filaggrin (FLG) and transepidermal water loss (TEWL) (assesses skin barrier integrity), S100A8 and S100A9 expression (assesses skin inflammation) and AD severity.
METHODS
We studied 400 children with AD in the Mechanisms of Progression from Atopic Dermatitis to Asthma in Children (MPAACH) cohort to identify groupings of food and aeroallergen sensitizations. MPAACH is a paediatric AD cohort, aged 1-2, recruited through hospital/community settings between 2016 and 2018. We analysed these groupings' associations with AD biomarkers: skin FLG, S100A8 and S100A9 expression, total IgE, TEWL and AD severity.
RESULTS
An unbiased machine learning approach revealed five allergen clusters. The most common cluster (N = 131), SPT
CONCLUSIONS AND CLINICAL RELEVANCE
In this largely clinic-based cohort of young children with AD, allergic sensitization to peanut, egg, cat or dog was associated with more severe disease and skin barrier function but not markers of cutaneous inflammation. These data need replicating in a population-based cohort but may have important implications for understanding the interaction between AD and allergic sensitization.

Identifiants

pubmed: 33721370
doi: 10.1111/cea.13866
pmc: PMC9258184
mid: NIHMS1817389
doi:

Substances chimiques

Calgranulin A 0
Calgranulin B 0
FLG protein, human 0
Filaggrin Proteins 0
S100A8 protein, human 0
S100A9 protein, human 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

666-673

Subventions

Organisme : NIAID NIH HHS
ID : U19 AI070235
Pays : United States
Organisme : Eunice Kennedy Shriver National Institute of Child Health and Human Development
ID : 5K12HD28827-27

Informations de copyright

© 2021 John Wiley & Sons Ltd.

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Auteurs

Michael G Sherenian (MG)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Division of Allergy and Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Arjun Kothari (A)

Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Jocelyn M Biagini (JM)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

John W Kroner (JW)

Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Asel Baatyrbek Kyzy (A)

Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Elisabet Johannson (E)

Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Gowtham Atluri (G)

Department of Electrical Engineering and Computer Science, University of Cincinnati, Cincinnati, OH, USA.

Hua He (H)

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Lisa J Martin (LJ)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

Gurjit K Khurana Hershey (GK)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Division of Allergy and Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

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