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Atopic Features and Inflammatory Markers Across Cassano-Graded Adenoid Hypertrophy
Fatih Kaplan1, Bilge Kurnaz Kaplan2, Abdulgani Gülyüz3
1Department of Pediatric Allergy and Immunology, Malatya Training and Research Hospital, 44000 Malatya, Türkiye.
Insights
Adenoid hypertrophy (AH) severity in children is linked to eosinophilia, not IgE sensitization. Eosinophil assessment can help evaluate AH severity.
Area of Science:
- Pediatric Otolaryngology
- Allergy and Immunology
- Respiratory Medicine
Background:
- Conflicting evidence exists regarding the association between adenoid hypertrophy (AH) and atopy.
- This study investigates whether Cassano-graded AH severity correlates more with inflammatory markers than IgE-mediated sensitization.
Purpose of the Study:
- To determine the association between adenoid hypertrophy severity and atopic features in children.
- To differentiate the roles of inflammatory markers versus IgE-mediated sensitization in AH severity.
Main Methods:
- Retrospective study of 426 children (aged 3-12) diagnosed with AH.
- Adenoid hypertrophy was graded using the Cassano classification (dichotomized as advanced AH: Stage III-IV).
- Atopic features assessed included clinical atopy, IgE sensitization, elevated total IgE, and eosinophilia; multivariable logistic regression was used.
Main Results:
- Advanced AH was independently associated with eosinophilia (aOR 2.07).
- Clinical atopy was linked to family history, elevated total IgE, and passive smoking.
- IgE-mediated sensitization was solely associated with family history of atopy.
Conclusions:
- Adenoid hypertrophy severity in children is associated with eosinophilia, not IgE-mediated sensitization.
- Eosinophil assessment may improve routine evaluation of AH severity.
Background:
Evidence linking adenoid hypertrophy (AH) and atopy is conflicting. We examined whether Cassano-graded AH severity is more closely associated with inflammatory markers than with IgE-mediated sensitization.
Methods:
We retrospectively included children aged 3-12 years diagnosed with AH between December 2022 and December 2025. AH was graded according to the Cassano classification and dichotomized as advanced AH (Stage III-IV). Atopic features were evaluated separately as clinical atopy, IgE-mediated sensitization, elevated total IgE, and eosinophilia. Multivariable logistic regression analyses were performed to assess factors associated with clinical atopy, sensitization, and advanced AH.
Results:
Among 426 children, clinical atopy was present in 28.2%, sensitization in 23.0%, elevated total IgE in 16.4%, and eosinophilia in 27.7%; 39.2% had advanced AH. In multivariable analysis, clinical atopy was independently associated with family history of atopy (aOR 13.9; 95% CI 7.9-24.4), elevated total IgE (aOR 3.86; 95% CI 2.10-7.08), and passive smoking exposure (aOR 1.73; 95% CI 1.07-2.79). Sensitization was independently associated only with family history of atopy (aOR 4.99; 95% CI 1.99-12.53). Advanced AH was independently associated only with eosinophilia (aOR 2.07; 95% CI 1.30-3.29).
Conclusions:
AH severity was associated with eosinophilia rather than classical IgE-mediated sensitization. Assessment of eosinophilia may aid routine severity evaluation in children with AH.
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