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The Roles of Human Microbiome and Vitamin D in the Development of Childhood Allergic Diseases

The Roles of Human Microbiome and Vitamin D in the Development of Childhood Allergic Diseases

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05670262
Enrollment
6000
Registered
2023-01-04
Start date
2022-08-04
Completion date
2027-07-31
Last updated
2024-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric

Keywords

allergic diseases, birth cohort, human microbiome, vitamin D, vitamin D receptors and vitamin D binding protein

Brief summary

A birth cohort study to evaluate the role of human microbiome and vitamin D in the development of allergic diseases in young child before one year of age.

Detailed description

Allergic diseases are chronic inflammatory disorders that frequently affect young infants before one year of age, and is the beginning of allergy march in later life. The prevalence is increasing in industrial world, Taiwan included. Genetic and environmental factors, such exposure to allergens and microbes, especially early in life, have a detrimental role in the development of allergic diseases, such as atopic dermatitis (AD), allergic rhinitis and asthma. Vitamin D has an important role in different allergic disease. Lower cord blood vitamin D status was observed in infants that developed eczema. Vitamin D binding protein (DBP) bound to vitamin D and regulated its metabolites in the circulation. Moreover, vitamin D receptors have been identified on nearly all cells of the immune system. It may contribute to maintenance of intestinal barrier function by preventing increased intestinal permeability, dysbiosis, inflammation, and a lack of immune tolerance in the gut. Although aberrant interactions between gut microbes and the intestinal immune system have been implicated in this allergic disease, however, the causal effect of microbiota colonization of the gut and vitamin D that influence the development of allergic diseases, such as AD, in young infants is still unknown. The investigators plan to design a birth cohort study to evaluate the role of human microbiome and vitamin D in the development of allergic diseases in young child before one year of age. In this study, the investigators will recruit mother-infant pairs in antenatal clinics in China Medical University Hospital and China Medical University Children's Hospital. Newborns who have been enrolled at birth are collected for meconium samples before discharged from nursery and eligible for follow-up visits, and collect their nasal and anal swab microbiome samples at 2 and 12 months follow-up visit. Parental questionnaires are collected at 6, and 12 months of age. All infants were assessed at birth, 2 and 6, and 12 months of age. Assessment included physical examination for allergic diseases. In addition, infants at 12 months of age were collected their 3cc of blood sample. The investigators believe this longitudinal and prospective study, to follow-up infants from the date of birth until one years old, can answer the cause-effect relationships of microbiota and vitamin D in the development of allergic diseases, and design a microbiota-related preventive and treatment strategy.

Interventions

None listed

Sponsors

China Medical University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Years to 1 Years
Healthy volunteers
Yes

Inclusion criteria

* All term newborn babies who are born in China Medical University Hospital. The term baby defines the maternal gestational age between 37 0/7 weeks to 41 6/7 weeks.

Exclusion criteria

* The

Design outcomes

Primary

MeasureTime frameDescription
Levels of vitamin DMonth 12Vitamin D will be measured in a blood sample by ELISA.
Total immunoglobulin E (IgE)Month 12Plasma total IgE concentration will be measured by microparticle immunoassay (IMx analyzer, Abbott Laboratories, Abbott Park, IL) and ELISA.
Allergen-specific immunoglobulin E (IgE)Month 12Plasma allergen-specific IgE will be measured by BioIC ®.
Single nucleotide polymorphism of vitamin D receptor and vitamin D binding proteinMonth 12Single nucleotide polymorphism (SNP) genotyping will be performed in a blood sample by using TaqMan SNP genotyping assays.
MicrobiomeMonth 0Meconium samples will be used to detect intestinal microbiome by using 16S rRNA sequencing to determine baseline status.

Secondary

MeasureTime frameDescription
Parental questionnaire (6-12 month)Month 12For assessing child's health, feeding habit, and environmental exposure
Parental questionnaire (0-6 month)Month 6For assessing child's health, feeding habit, and environmental exposure

Countries

Taiwan

Contacts

Primary ContactJiu-Yao Wang, MD
aim.cmuh@gmail.com886422052121

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026