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Published on: June 4, 2017
Clinical and molecular analysis of longitudinal rhinitis phenotypes in an urban birth cohort
Sima K Ramratnam1, Molly Johnson2, Cynthia M Visness2
1Department of Pediatrics, University of Wisconsin-Madison, Madison, Wis.
Insights
Childhood chronic rhinitis has distinct symptom patterns linked to specific risk factors and immune responses. Identifying these phenotypes early may help prevent rhinitis and related allergic conditions.
Area of Science:
- Pediatric Allergy and Immunology
- Respiratory Medicine
- Genetics and Genomics
Background:
- Chronic rhinitis in children presents heterogeneously, posing a significant health burden.
- Understanding distinct phenotypes and their underlying biology is crucial for targeted interventions.
Purpose of the Study:
- Identify longitudinal rhinitis symptom patterns in childhood.
- Examine associations with early life factors, allergic conditions, and gene expression.
Main Methods:
- Evaluated rhinitis symptoms in 485 urban children (ages 1-11) from the URECA birth cohort.
- Identified longitudinal rhinitis phenotypes.
- Assessed relationships with early exposures, atopic comorbidities, and nasal gene expression at age 11.
Main Results:
- Four rhinitis phenotypes were identified: low/minimal, persistent, persistent decreasing, and late increasing.
- Persistent rhinitis correlated with allergic sensitization and asthma.
- Risk factors for persistent rhinitis included frequent colds, antibiotic use, and reduced indoor allergen exposure.
- Rhinitis phenotypes showed distinct patterns in type 2 and immune response gene expression.
Conclusions:
- Rhinitis symptoms in urban children often precede aeroallergen sensitization.
- Symptom-based rhinitis phenotypes exhibit unique risk factors and nasal transcriptomes.
- Targeting early life factors and immune mechanisms could prevent childhood chronic rhinitis.
Background:
Chronic rhinitis symptoms cause significant health burden among children and can have a heterogeneous presentation. Defining phenotypes of childhood chronic rhinitis and associated pathobiology may lead to prevention or improved treatments.
Objectives:
We sought to identify longitudinal patterns of rhinitis symptoms in childhood and determine their associations with early life risk factors, allergic comorbidities, and nasal epithelial cell gene expression.
Methods:
Chronic rhinitis symptoms were evaluated from ages 1 through 11 years in 485 urban children at high risk for allergic disease in the URECA (Urban Environment and Childhood Asthma) birth cohort. We identified longitudinal rhinitis phenotypes and their relationships to early life exposures, atopic comorbidities, and patterns of nasal epithelial gene expression at age 11 years.
Results:
Chronic rhinitis symptoms started early in many children and were a risk factor for developing aeroallergen sensitization. We identified 4 longitudinal rhinitis phenotypes: low/minimal, persistent, persistent decreasing, and late increasing. Persistent rhinitis was most closely linked to allergic sensitization and asthma. Risk factors for persistent rhinitis included frequent colds (P < .001), antibiotic use (P < .001), and reduced exposure to common indoor aeroallergens (P = .003). Compared to low/minimal rhinitis phenotype, the other rhinitis phenotypes were associated with increased expression of canonical type 2 genes and decreased expression of immune response genes.
Conclusions:
In urban children, rhinitis symptoms often precede aeroallergen sensitization. Rhinitis phenotypes based on symptoms had distinct risk factors and nasal transcriptome. These results suggest that focusing on early life risk factors and distinct immune mechanisms may be a target to preventing chronic rhinitis in childhood.
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