Background: Asthma is the most frequent chronic disease in children. One of the most replicated genetic findings in childhood asthma is the gene confirmed in several GWA studies in several pediatric populations.
Objectives: The purpose of this study was to analyze variants and expression in childhood asthma in the Polish population.
Methods: In the study we included 416 subject, 223 asthmatic children and 193 healthy control subjects. The analysis of two SNPs (rs3744246 and rs8076131) was performed using genotyping with TaqMan probes. The methylation of the promoter was examined with Methylation Sensitive HRM (MS-HRM), covering 9 CpG sites. The expression of was analyzed in PBMCs from pediatric patients diagnosed with allergic asthma and primary human bronchial epithelial cells derived from healthy subjects treated with IL-13, IL-4, or co-treatment with both cytokines to model allergic airway inflammation.
Results: We found that expression was increased in allergic asthma both in PBMCs from asthmatic patients as well as in human bronchial epithelial cells stimulated with the current cytokines. We did not observe significant differences between cases and controls either in the genotype distribution of analyzed SNPs (rs3744246 and rs8076131) nor in the level of promoter methylation.
Conclusions: Increased expression is associated with pediatric allergic asthma and upregulated in the airways upon Th2-cytokines stimulation, but further functional studies are required to fully understand its role in this disease.
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| http://dx.doi.org/10.1080/02770903.2022.2056896 | DOI Listing |
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