Increase in eosinophil-derived neurotoxin level in school children with allergic disease.

Allergic rhinitis Atopic dermatitis Biomarkers Bronchial asthma Eosinophil-derived neurotoxin Food allergy

Journal

Asia Pacific allergy
ISSN: 2233-8276
Titre abrégé: Asia Pac Allergy
Pays: Netherlands
ID NLM: 101561954

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 02 06 2022
accepted: 12 07 2022
entrez: 15 8 2022
pubmed: 16 8 2022
medline: 16 8 2022
Statut: epublish

Résumé

Eosinophils are major effector cells of allergic disease and excellent markers of eosinophilic inflammation. Accurate and reliable biomarkers are helpful in the diagnosis, treatment, and control of allergic disease. This study aimed to investigate an alternate marker of eosinophilic inflammation, eosinophil-derived neurotoxin (EDN), in a number of allergic diseases. Three hundred ninety-six elementary school-age children with various allergic conditions were recruited for this study. Subgroups included food allergies (FAs), atopic dermatitis (AD), bronchial asthma (BA), and allergic rhinitis (AR). EDN levels in these groups were compared to those in 93 healthy controls (HC). All subjects with allergic disease had elevated levels of serum EDN (median [interquartile range]: FA, 124.2 ng/mL [59.13-160.5 ng/mL]; AD, 110.8 ng/mL [57.52-167.9 ng/mL]; BA, 131.5 ng/mL [60.60-171.0 ng/mL]; AR, 91.32 ng/mL [46.16-145.0 ng/mL]) compared to HC (38.38 ng/mL [32.40-55.62 ng/mL]) ( Direct measures of eosinophilic inflammation are needed for accurate diagnosis, treatment, and monitoring of allergic diseases. EDN may be a worthy biomarker of eosinophil activity and a useful screening tool for allergic diseases including FA, AD, BA, and AR.

Sections du résumé

Background UNASSIGNED
Eosinophils are major effector cells of allergic disease and excellent markers of eosinophilic inflammation. Accurate and reliable biomarkers are helpful in the diagnosis, treatment, and control of allergic disease.
Objective UNASSIGNED
This study aimed to investigate an alternate marker of eosinophilic inflammation, eosinophil-derived neurotoxin (EDN), in a number of allergic diseases.
Methods UNASSIGNED
Three hundred ninety-six elementary school-age children with various allergic conditions were recruited for this study. Subgroups included food allergies (FAs), atopic dermatitis (AD), bronchial asthma (BA), and allergic rhinitis (AR). EDN levels in these groups were compared to those in 93 healthy controls (HC).
Results UNASSIGNED
All subjects with allergic disease had elevated levels of serum EDN (median [interquartile range]: FA, 124.2 ng/mL [59.13-160.5 ng/mL]; AD, 110.8 ng/mL [57.52-167.9 ng/mL]; BA, 131.5 ng/mL [60.60-171.0 ng/mL]; AR, 91.32 ng/mL [46.16-145.0 ng/mL]) compared to HC (38.38 ng/mL [32.40-55.62 ng/mL]) (
Conclusions UNASSIGNED
Direct measures of eosinophilic inflammation are needed for accurate diagnosis, treatment, and monitoring of allergic diseases. EDN may be a worthy biomarker of eosinophil activity and a useful screening tool for allergic diseases including FA, AD, BA, and AR.

Identifiants

pubmed: 35966157
doi: 10.5415/apallergy.2022.12.e25
pmc: PMC9353201
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e25

Informations de copyright

Copyright © 2022. Asia Pacific Association of Allergy, Asthma and Clinical Immunology.

Déclaration de conflit d'intérêts

Conflict of Interest: The authors have no financial conflicts of interest.

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Auteurs

Chang-Keun Kim (CK)

Asthma & Allergy Center, Department of Pediatrics, Inje University Sanggye Paik Hospital, Seoul, Korea.

Dong Yoon Kang (DY)

Department of Preventive Medicine, Seoul National University College of Medicine, Seoul, Korea.

Zak Callaway (Z)

Asthma & Allergy Center, Department of Pediatrics, Inje University Sanggye Paik Hospital, Seoul, Korea.
Department of Biomedical Science, School of Biological Sciences, University of Ulsan, Ulsan, Korea.

Kyoung Soo Kim (KS)

Department of Clinical Pharmacology and Therapeutics, Kyung Hee University School of Medicine, Seoul, Korea.

Eun Mi Kwon (EM)

Asthma & Allergy Center, Department of Pediatrics, Inje University Sanggye Paik Hospital, Seoul, Korea.

Fumiya Yamaide (F)

Department of Pediatrics, Graduate School of Medicine, Chiba University, Chiba, Japan.

Taiji Nakano (T)

Department of Pediatrics, Graduate School of Medicine, Chiba University, Chiba, Japan.

Yoichi Suzuki (Y)

Department of Public Health, Graduate School of Medicine, Chiba University, Chiba, Japan.

Yoichi Mashimo (Y)

Department of Public Health, Graduate School of Medicine, Chiba University, Chiba, Japan.

Akira Hata (A)

Department of Public Health, Graduate School of Medicine, Chiba University, Chiba, Japan.

Yoshitaka Okamoto (Y)

Department of Otorhinolaryngology and Head and Neck Surgery, Graduate School of Medicine, Chiba, Japan.
Chiba Rosia Hospital, Chiba, Japan.

Naoki Shimojo (N)

Center for Preventive Medical Sciences, Chiba University, Chiba, Japan.

Classifications MeSH