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Published on: August 7, 2017
Risk factors for infantile atopic dermatitis and recurrent wheezing
N Kawamoto1, T Fukao, H Kaneko
1Department of Pediatrics, Graduate School of Medicine, Gifu University, Gifu, Japan. noriok-gif@umin.ac.jp
Insights
Cord blood immunoglobulin E (IgE) is a risk factor for infant atopic dermatitis (AD). Later, total IgE and egg white sensitization predict AD, while interleukin 4 (IL-4) predicts recurrent wheezing (RW).
Area of Science:
- Immunology
- Pediatrics
- Allergy
Background:
- The precise pathogenic mechanisms underlying atopic dermatitis (AD) and recurrent wheezing (RW) in infants remain incompletely understood.
- Identifying early immunological risk factors is crucial for understanding disease development.
Purpose of the Study:
- To investigate immunological markers associated with the development of AD and RW in infancy.
- To identify potential early predictors for these common childhood conditions.
Main Methods:
- A prospective cohort study followed 314 infants from birth to 14 months.
- Immunological markers were assessed via blood tests at 6 and 14 months.
- Logistic regression and receiver operating characteristic analyses identified risk factors.
Main Results:
- Cord blood immunoglobulin E (IgE) was linked to AD at 6 months (aOR, 1.607).
- At 6 months, total IgE (aOR, 1.018) and egg white sensitization (aOR, 23.246) predicted AD at 14 months.
- Phytohemagglutinin (PHA)-induced interleukin 4 (IL-4) production by peripheral blood mononuclear cells (PBMCs) at 6 months predicted RW at 14 months (aOR, 1.043).
Conclusions:
- Elevated cord blood IgE is an early risk factor for infant AD.
- At 6 months, total IgE levels and specific IgE sensitization to egg white are significant predictors of AD by 14 months.
- PHA-induced IL-4 production in PBMCs at 6 months serves as a risk factor for developing RW later in infancy.
Background:
The pathogenic mechanisms of atopic dermatitis (AD) and recurrent wheezing (RW) during infancy are not fully understood.
Objective:
We evaluated immunological markers associated with AD and RW during infancy.
Methods:
We followed a cohort (n = 314) from birth to 14 months of age. Some of the participants underwent a physical examination and blood test at 6 and 14 months of age. Univariate and multivariate logistic regression analysis and receiver operating characteristic curve analysis were performed to find which immunological markers could be risk factors for AD and RW.
Results:
Of 16 immunological markers found in cord blood, only immunoglobulin (Ig) E was associated with AD at 6 months of age (adjusted OR [aOR], 1.607). None of the markers was associated with AD or RW at 14 months of age. Of 23 immunological markers at 6 months of age, total IgE (aOR, 1.018) and sensitization to egg white (aOR, 23.246) were associated with AD at 14 months of age. Phytohemagglutinin (PHA)-induced production of interleukin (IL) 4 from peripheral blood mononuclear cells (PBMCs) (aOR, 1.043) was associated with RW at 14 months of age.
Conclusion:
Cord blood IgE was a risk factor for AD at 6 months of age. Total IgE and sensitization to egg white at 6 months of age were risk factors for AD at 14 months of age. PHA-induced IL-4 production in PBMCs at 6 months of age was a risk factor for RW at 14 months of age.
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