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Published on: August 7, 2017
Elevated cord blood IgE is associated with recurrent wheeze and atopy at 7 yrs in a high risk cohort
Alexander Ferguson1, Helen Dimich-Ward, Allan Becker
1Division of Allergy, Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.
Insights
Detecting immunoglobulin E (IgE) in cord blood may help identify infants at high risk for developing allergic diseases. This cord blood IgE measure shows potential for primary prevention strategies in atopic children.
Area of Science:
- Immunology
- Pediatrics
- Allergy Research
Background:
- Primary prevention of atopic diseases requires identifying high-risk children early.
- Family history is a key indicator for children at increased risk of allergic diseases.
Purpose of the Study:
- To evaluate risk factors associated with detectable cord blood IgE (CB-IgE).
- To assess the predictive value of CB-IgE for asthma and other IgE-mediated allergic diseases in high-risk children.
Main Methods:
- Cord blood samples were collected from infants enrolled in a primary prevention randomized controlled trial.
- CB-IgE levels were measured and analyzed for associations with perinatal risk factors.
- The cohort was followed up to age 7 to assess atopic disorder development and the predictive utility of CB-IgE.
Main Results:
- Detectable CB-IgE (≥0.5 kU/l) was found in 19.3% of infants.
- Maternal atopy and winter birth were identified as risk factors for detectable CB-IgE.
- CB-IgE was significantly associated with allergic sensitization (OR 2.22) and recurrent wheeze at age 7 (OR 2.51).
Conclusions:
- CB-IgE may serve as a valuable biomarker for identifying infants predisposed to atopic diseases.
- This finding supports the use of CB-IgE in primary prevention programs for allergic conditions.
Abstract:
There is considerable interest in identifying children at high risk for developing atopic diseases for primary prevention. This study evaluates risk factors for detectable cord blood IgE and assesses CB-IgE in predicting asthma and other IgE-mediated allergic diseases in children at high risk because of family history. Cord blood was obtained as part of a randomized controlled trial assessing the efficacy of an intervention program in the primary prevention of IgE-mediated allergic diseases. CB-IgE was measured and the degree to which this was associated with perinatal risk factors was assessed. The cohort was then evaluated for atopic disorders at 7 yrs of age to assess the predictive value of CB-IgE. Fifty-five (19.3%) of infants had detectable CB-IgE (>/=0.5 kU/l). Maternal atopy and birth in winter months were risk factors associated with detectable CB-IgE. CB-IgE was found to be significantly associated with allergic sensitization (OR 2.22; 95% CI 1.11, 4.41) and recurrent wheeze at 7 yrs (OR 2.51, 95% CI 1.09, 5.76) but not with other outcomes. CB-IgE may be a useful measure for identifying children at high risk of atopic diseases for the purpose of primary prevention.
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