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IL17F rs763780 single nucleotide polymorphism is associated with asthma after bronchiolitis in infancy
Annukka Holster1, Johanna Teräsjärvi2, Alex-Mikael Barkoff2
1Center for Child Health Research, Faculty of Medicine and Life Sciences, University of Tampere and University Hospital, Tampere, Finland.
Insights
This study investigated Interleukin-17F (IL-17F) gene variations and childhood asthma risk following infant bronchiolitis. The IL17F rs763780 polymorphism was linked to increased asthma medication use and atopic dermatitis in children.
Area of Science:
- Immunogenetics
- Pediatric Respiratory Medicine
- Allergy and Immunology
Background:
- Interleukin-17F (IL-17F) is implicated in asthma pathogenesis.
- Infant bronchiolitis is a significant risk factor for developing childhood asthma.
- Genetic predispositions, including IL-17F polymorphisms, may influence asthma development post-bronchiolitis.
Purpose of the Study:
- To evaluate the association between specific IL17F gene polymorphisms (rs763780, rs11465553, rs7741835) and the risk of childhood asthma.
- To assess these genetic associations in children with a history of bronchiolitis in infancy.
- To determine if IL17F variations correlate with asthma and allergy outcomes at school age.
Main Methods:
- A prospective long-term follow-up study included 166 children hospitalized for bronchiolitis before six months of age.
- Children attended follow-up visits at 5-7 and 11-13 years of age for asthma and allergy assessments.
- Genotyping for IL17F polymorphisms rs763780, rs11465553, and rs7741835 was performed on blood samples from 165 participants.
Main Results:
- No significant association was found between IL17F rs11465553 or rs7741835 and asthma or allergy outcomes.
- Children with the variant IL17F rs763780 genotype showed significantly higher use of inhaled corticosteroids (ICSs) between ages 5-7 and 11-13 years (adjusted OR 3.58).
- The variant IL17F rs763780 genotype was also associated with a higher reported incidence of doctor-diagnosed atopic dermatitis at 11-13 years (adjusted OR 2.71).
Conclusions:
- The IL17F rs763780 polymorphism may be associated with asthma development and related allergic conditions in children with a history of infant bronchiolitis.
- This finding provides preliminary evidence linking specific IL-17F genetic variations to long-term respiratory health outcomes.
- Further research is warranted to elucidate the precise role of IL17F rs763780 in the trajectory from infant bronchiolitis to childhood asthma.
Aim:
Interleukin-17F (IL-17F) is involved with asthma. The aim of this study was to evaluate the association of IL17F polymorphisms with childhood asthma after bronchiolitis in infancy.
Methods:
We invited 166 children who were hospitalised for bronchiolitis at younger than 6 months of age to follow-up visits at 5-7 years and 11-13 years of ages. Asthma and allergy diagnoses, asthma-presumptive symptoms and use of inhaled corticosteroids (ICSs) were registered. Blood samples were available for IL17F rs763780 (T/C), rs11465553 (C/T) and rs7741835 (C/T) determinations in 165 cases.
Results:
The presence of IL17F rs11465553 and rs7741835 variations showed no significant associations with any asthma or allergy outcome at either 5-7 years or 11-13 years of ages. Instead, children with the variant IL17F rs763780 genotype had used more often ICSs between the follow-up visits from 5-7 to 11-13 years (adjusted OR 3.58) than those with the wild genotype. Children with the variant IL17F rs763780 genotype reported more often doctor-diagnosed atopic dermatitis (adjusted OR 2.71) at 11-13 years of age than those with the wild genotype.
Conclusion:
This prospective long-term follow-up study provided preliminary evidence on the association of the IL17F rs763780 polymorphism with asthma at school age after bronchiolitis in infancy.
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