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Published on: September 27, 2017
Phenotypes of atopic dermatitis identified by cluster analysis in early childhood
Euri Seo1, Jisun Yoon2, Sungsu Jung3
1Department of Pediatrics, Dongguk University Ilsan Hospital, Dongguk University College of Medicine, Goyang, Korea.
Insights
Atopic dermatitis in young children presents diverse clinical phenotypes. Identifying these subtypes, like those with high eosinophils or specific allergen sensitivities, is crucial for understanding disease heterogeneity.
Area of Science:
- Dermatology
- Pediatrics
- Immunology
Background:
- Atopic dermatitis is a chronic inflammatory skin condition with variable clinical presentations.
- Disease course and treatment efficacy in atopic dermatitis can be influenced by distinct phenotypes and endotypes.
- Understanding early childhood atopic dermatitis phenotypes is essential for personalized management.
Purpose of the Study:
- To identify and characterize distinct clinical phenotypes of atopic dermatitis in children under three years of age.
- To explore the relationship between clinical presentation, biomarkers, and allergen sensitization in early childhood atopic dermatitis.
- To investigate the heterogeneity of atopic dermatitis even in the early stages of the disease.
Main Methods:
- Cluster analysis was performed on data from 572 children under three years old diagnosed with atopic dermatitis.
- Eleven clinical and laboratory variables were analyzed to identify distinct patient clusters.
- Predictive modeling was used to assess the strength of specific variables in classifying these phenotypes.
Main Results:
- Four distinct clinical phenotypes of early childhood atopic dermatitis were identified.
- Phenotypes were characterized by varying levels of blood eosinophils, immunoglobulin E, C-reactive protein, and allergen sensitization (food and inhalant).
- Age at onset, age at diagnosis, white blood cell count, eosinophil count, C-reactive protein, and serum total immunoglobulin E were key predictors, achieving 95.5% classification accuracy.
Conclusions:
- Atopic dermatitis exhibits significant heterogeneity even in early childhood, with identifiable clinical phenotypes.
- These findings underscore the importance of recognizing distinct subtypes for potentially tailored treatment strategies.
- The identified predictors offer a robust method for classifying atopic dermatitis phenotypes in young children.
Abstract:
Atopic dermatitis is a chronic, relapsing, inflammatory skin disease that usually appears in early childhood and develops into a heterogeneous disease during childhood. The clinical course and treatment for atopic dermatitis can differ according to its phenotype and/or endotype. This study aimed to identify clinical phenotypes of atopic dermatitis in early childhood. Data were obtained from 572 children under 3 years of age with atopic dermatitis. Cluster analysis applied to 11 variables, and we identified four clusters of atopic dermatitis. Children in cluster A (n = 141) had early-onset atopic dermatitis with high blood eosinophil counts, serum total immunoglobulin E and rates of sensitization to food allergens. Children in cluster B (n = 218) had early-onset atopic dermatitis with low blood eosinophil counts, serum total immunoglobulin E and rates of sensitization to both food and inhalant allergens. Children in cluster C (n = 53) had early-onset atopic dermatitis with high C-reactive protein levels and white blood cell counts. Children in cluster D (n = 160) had middle-onset atopic dermatitis with high serum total immunoglobulin E and rates of sensitization to inhalant allergens. Cluster A had the highest Scoring for Atopic Dermatitis and transepidermal water loss values. Age at onset, age at diagnosis, white blood cell count, eosinophil count, C-reactive protein and serum total immunoglobulin E level were the strongest predictors of cluster assignment. Analysis of these six variables alone resulted in correct classification of 95.5% of the subjects. These results support the heterogeneity of atopic dermatitis, even in early childhood.
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