Association of atopic dermatitis with obesity via a multi-omics approach: A protocol for a case-control study.
Biomarkers
/ blood
Body Mass Index
Case-Control Studies
Child
Child, Preschool
Dermatitis, Atopic
/ complications
Eosinophil Cationic Protein
/ blood
Feces
/ chemistry
Female
Gastrointestinal Microbiome
Humans
Immunoglobulin E
/ blood
Male
Metabolome
Obesity
/ complications
Quality of Life
Republic of Korea
Journal
Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R
Informations de publication
Date de publication:
Jul 2019
Jul 2019
Historique:
entrez:
24
7
2019
pubmed:
25
7
2019
medline:
2
8
2019
Statut:
ppublish
Résumé
Several studies have found that obesity is associated with atopic dermatitis (AD); however, the mechanisms underlying the association are largely unknown. This study aims to assess the association of AD with obesity in the Korean population and verify its mechanism via a multi-omics analysis. A case-control study will be conducted in the Republic of Korea. A total of 80 subjects, aged 4 to 12 years, matched for age and sex, with body mass index at or above the 85th percentile or at or below the 25th percentile, will be included. Subjects will be assigned to the following 4 groups: obese/overweight with AD, normal/underweight with AD, obese/overweight control, and normal/underweight control. Serum metabolome and immune biomarkers, as well as fecal metabolome and microbiome biomarkers, will be analyzed. Serum eosinophil cationic protein, total serum Immunoglobulin E (IgE), and specific IgE will be analyzed to assess allergic tendency. The SCORing of AD index, the children's dermatology life quality index, body composition analysis, and the Korean gastrointestinal symptom rating scale will be obtained to assess the disease status and severity of the subjects. The findings of this study are expected to provide evidence of an association between AD and obesity via a gut microbiome-metabolome-immune mechanism. Therefore, it may improve future management strategies for AD. This study has been registered at the Korean National Clinical Trial Registry, Clinical Research Information Service (KCT0003630).
Identifiants
pubmed: 31335732
doi: 10.1097/MD.0000000000016527
pii: 00005792-201907190-00067
pmc: PMC6708792
doi:
Substances chimiques
Biomarkers
0
Immunoglobulin E
37341-29-0
Eosinophil Cationic Protein
EC 3.1.27.-
RNASE3 protein, human
EC 3.1.27.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e16527Références
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