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A case-control study for comorbidity and laboratory factors associated with food-induced anaphylaxis
Eli Magen1, Eugene Merzon1, Ilan Green1
1From the Leumit Health Services, Tel Aviv-Yafo, Israel.
Insights
Food-induced anaphylaxis (FIA) in children is linked to higher eosinophil and IgE levels, and more allergic diseases like asthma and eczema. Interestingly, parasitic infections like enterobiasis showed a protective effect against FIA.
Area of Science:
- Pediatric Allergy and Immunology
- Epidemiology
- Clinical Research
Background:
- Food-induced anaphylaxis (FIA) is a severe allergic reaction to food allergens.
- Understanding associated factors is crucial for managing pediatric FIA.
- This study focuses on comorbidities and laboratory findings in Israeli children.
Purpose of the Study:
- To investigate comorbidities and laboratory factors associated with pediatric FIA.
- To compare these factors between children with FIA and those with food allergy but no anaphylaxis.
- To provide epidemiological insights into FIA in a specific pediatric population.
Main Methods:
- A case-control study design was employed.
- Retrospective data from 711 pediatric FIA cases and 2560 controls were analyzed.
- Comorbidities were identified via diagnosis codes; laboratory data were compared.
Main Results:
- FIA patients exhibited higher eosinophil counts, elevated immunoglobulin E (IgE) and IgA levels.
- Increased prevalence of allergic diseases including allergic rhinitis, asthma, atopic dermatitis, and angioedema was observed in the FIA group.
- A negative association was found between helminthiases (e.g., enterobiasis) and FIA.
Conclusions:
- Pediatric FIA is associated with specific laboratory markers and a higher burden of allergic comorbidities.
- The findings highlight the complex interplay of immune factors and environmental exposures in FIA.
- This research contributes valuable epidemiological data on FIA in children.
Abstract:
Background: Food-induced anaphylaxis (FIA) is a serious and potentially life-threatening allergic reaction triggered by food allergens. Objective: This case-control study aimed to investigate comorbidities and laboratory factors associated with FIA in the pediatric population of Israel. Methods: Retrospective data from the electronic health records of Leumit Health Care Services were used to identify 711 pediatric patients with FIA and 2560 subjects with food allergy and without anaphylaxis matched for age, gender, and ethnicity. Comorbidities were identified based on medical billing diagnosis codes, and laboratory characteristics were compared between the two groups. Results: The mean ± standard deviation age of patients with FIA was 4.1 ± 4.1 years, and 37.3% were girls. Laboratory analysis revealed increased eosinophil counts (p < 0.001), elevated immunoglobulin E (IgE) (p < 0.001), and IgA levels (p = 0.001) in the FIA group compared with the controls. With regard to comorbidities, the FIA group had higher prevalence rates of allergic diseases, including allergic rhinitis (odds ratio [OR] 1.72; p < 0.001), allergic conjunctivitis (OR 1.84; p = 0.001), asthma (OR 1.36; p < 0.001), angioedema (OR 6.37; p < 0.001), atopic dermatitis (OR 1.77; p < 0.001), and contact dermatitis (OR 1.42; p = 0.001). There was a trend toward significance for chronic spontaneous urticaria (p = 0.051). There was a significant negative association between helminthiases, particularly enterobiasis, and FIA (OR 0.76 [95% confidence interval, 0.59-0.98]; p = 0.029). Conclusion: This study provides valuable epidemiologic evidence on the associations among FIA, comorbidities, and laboratory factors in the pediatric population.
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