IL-1β and iNOS can drive the asthmatic comorbidities and decrease of lung function in perennial allergic rhinitis

Myung Woul Han1, Song Hee Kim2, Inbo Oh3

  • 1Department of Otolaryngology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Republic of Korea. brightmoon@uuh.ulsan.kr.

Insights

Interleukin-1β (IL-1β) and inducible nitric oxide synthase (iNOS) indicate asthma comorbidity in children with perennial allergic rhinitis (PAR). Higher levels correlate with reduced lung function, suggesting early intervention targets.

Area of Science:

  • Immunology
  • Pediatric Allergy
  • Respiratory Medicine

Background:

  • Allergic rhinitis (AR) and asthma frequently coexist, necessitating early detection of this comorbidity.
  • Identifying early indicators can facilitate timely treatment and prevent asthma progression in AR patients.
  • Perennial allergic rhinitis (PAR) affects children, with a subset developing asthma.

Purpose of the Study:

  • To investigate the role of interleukin-1β (IL-1β) and inducible nitric oxide synthase (iNOS) in PAR-asthma comorbidity.
  • To assess the association of IL-1β and iNOS with lung function in children with PAR.
  • To explore biomarkers including IL-1β, iNOS, and epithelial-mesenchymal transition (EMT) markers in Korean children.

Main Methods:

  • Analyzed a cohort of 240 Korean children (6-10 years) with PAR (PAR alone vs. PAR and asthma).
  • Measured serum levels of IL-1β, CCL-24, E-cadherin, and vimentin using ELISA.
  • Quantified epithelial iNOS using a NOS kit and examined blood eosinophils and IgE.

Main Results:

  • Elevated serum IL-1β, iNOS, and vimentin levels were significant indicators of PAR-asthma comorbidity.
  • Higher concentrations of IL-1β, iNOS, and vimentin correlated with reduced lung function in PAR children.
  • IL-1β expression related to E-cadherin, vimentin, and CCL-24; no correlation found between IL-1β and iNOS.

Conclusions:

  • IL-1β and iNOS serve as potential biomarkers for PAR-asthma progression and decreased lung function.
  • These biomarkers suggest possible targets for early intervention strategies in pediatric respiratory conditions.
  • Prompt identification of these markers may aid in preventing asthma development in children with PAR.
Abstract

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