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Atopic dermatitis is associated with a fivefold increased risk of polysensitisation in children
Suzanne A Broeks1, Paul L P Brand2,3
1Department of Internal Medicine, ZGT Hospital, Almelo, The Netherlands.
Insights
Children with atopic dermatitis have a significantly higher risk of polysensitisation, meaning they are sensitised to five or more allergens. This finding supports the theory of a compromised skin barrier facilitating allergen exposure.
Area of Science:
- Allergy and Immunology
- Dermatology
- Pediatrics
Background:
- A dysfunctional skin barrier in atopic dermatitis may lead to increased allergen exposure.
- Polysensitisation, defined as allergic sensitisation to five or more allergens, is a growing concern.
Purpose of the Study:
- To investigate the association between atopic dermatitis and the likelihood of polysensitisation in children.
- To determine if atopic dermatitis increases the risk of developing allergies to multiple common allergens.
Main Methods:
- Retrospective analysis of electronic hospital records for 1743 children (aged 0-17) with allergic symptoms.
- Measurement of specific immunoglobulin E (IgE) levels against 10 common inhaled and food allergens.
- Comparison of polysensitisation rates between children with and without atopic dermatitis, adjusting for age and gender.
Main Results:
- Polysensitisation was significantly more prevalent in children with atopic dermatitis (22.4%) compared to those without (5.5%, p < 0.001).
- Atopic dermatitis was independently associated with an increased odds of polysensitisation (OR: 5.63, 95% CI: 3.77-8.40).
- Other skin disorders did not demonstrate a similar increased risk for polysensitisation.
Conclusions:
- Polysensitisation is considerably more common in children diagnosed with atopic dermatitis.
- These findings support the hypothesis that a defective skin barrier in atopic dermatitis facilitates allergen sensitisation.
- The increased risk of polysensitisation appears specific to atopic dermatitis.
Aim:
It has been hypothesised that in atopic dermatitis, the dysfunctional skin barrier facilitates the transcutaneous presentation of allergens to the immune system. This study examined whether atopic dermatitis increased the likelihood of polysensitisation, namely sensitisation to five or more allergens.
Methods:
We examined the electronic hospital charts of 1743 children aged 0-17 years who had visited primary or secondary care physicians with allergic symptoms, whose blood was examined for the presence of specific immunoglobulin E (IgE) to the 10 most common inhaled and food allergens and whose files contained documentation of the presence of atopic dermatitis and other skin disorders. Sensitisation was defined as a specific IgE level of ≥0.35 kU/L.
Results:
Polysensitisation was more common in children with atopic dermatitis (268/1197, 22.4%) than those without (30/546, 5.5%, p < 0.001). This remained significant after adjustment for gender and age in a multiple logistic regression model (odds ratio: 5.63, 95% confidence interval 3.77-8.40). Other skin disorders did not show an increased risk of polysensitisation (5/97, 5.2%).
Conclusion:
Polysensitisation was considerably more common in children with atopic dermatitis than those without. This supports the hypothesis that sensitisation occurs through a defective skin barrier and appears to be specific for atopic dermatitis.
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