Role of IL13 genetic polymorphism in the development of bronchial asthma in children

S. Tereschenko, M. Smolnikova, E. Kasparov, E. Shakhtshneider, M. A. Malinchik, O. Konopleva, S. Smirnova
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Abstract

Bronchial asthma is a multifactorial disease, with both environmental factors and genetic predisposal affecting its development. A number of gene associations have been obtained between polymorphisms of cytokine genes produced by different types of immune cells and asthma development. Interleukin-13 is involved in allergic inflammation, increased bronchial hypersensitivity, regulation of eosinophil levels and IgE production by B cells, thus making it promising for studying IL13 gene polymorphisms in bronchial asthma coupled to development of the disease. The aim of this study was to investigate possible association between asthma and IL13 rs1800925 polymorphism in the children of Caucasian origin in Eastern Siberia. Four groups of patients with asthma were examined (mean age 12.8±1.2 years): with a controlled (n = 95) and uncontrolled course (n = 107), with severe (n = 71) and moderate severity (n = 131) diseases. The control group consisted of healthy individuals: children (n = 33) and adults (n = 102). DNA was isolated with sorbent method; genotyping was carried out using RT-PCR using specific oligonucleotide primers and fluorescent TaqMan probes. The allele and genotype frequencies were compared by the χ-square test using an online calculator. The odds ratio (OR) with a 95% confidence interval (CI) was performed to link genetic markers with pathological phenotypes. The CT IL13 rs1800925 genotype was shown to be associated with moderate asthma and cases of uncontrollable clinical course, whereas the TT genotype was associated with severe asthma. Thus, rs1800925 polymorphism of IL13 gene (the T* variant is known to be associated with increased IL-13 expression) may be associated with bronchial asthma in children. Our data are consistent with results of other authors. E.g., Liu Z. et al. revealed an association between rs1800925 IL13 and the risk of developing asthma in children, with CT and TT genotypes being more common in the patient group. Radhakrishnan A. et al., was studied rs1800925 IL13 in adult population of Malaysia and found that the T* allele frequency in the group of patients significantly exceeds the frequency of this allele in the control group. Thus, the results of our study showed that IL13 rs1800925 polymorphism is associated with bronchial asthma in children, especially, with level of its control and severity of the disease.
IL13基因多态性在儿童支气管哮喘发病中的作用
支气管哮喘是一种多因素疾病,环境因素和遗传易感性都影响其发展。不同类型的免疫细胞产生的细胞因子基因多态性与哮喘发展之间存在许多基因关联。白细胞介素-13参与变应性炎症、支气管超敏反应增加、嗜酸性粒细胞水平调节和B细胞产生IgE,因此研究il -13基因多态性与支气管哮喘的发展有希望。本研究的目的是调查东西伯利亚高加索裔儿童哮喘与IL13 rs1800925多态性之间的可能关联。四组哮喘患者(平均年龄12.8±1.2岁):控制病程(n = 95)和未控制病程(n = 107),严重病程(n = 71)和中度病程(n = 131)。对照组由健康个体组成:儿童(n = 33)和成人(n = 102)。用吸附法分离DNA;利用特异性寡核苷酸引物和荧光TaqMan探针进行RT-PCR分型。等位基因和基因型频率的比较采用χ 2检验,使用在线计算器。采用95%置信区间(CI)的比值比(OR)将遗传标记与病理表型联系起来。CT IL13 rs1800925基因型与中度哮喘和不可控临床病程相关,而TT基因型与重度哮喘相关。因此,IL-13基因rs1800925多态性(已知与IL-13表达升高相关的T*变异)可能与儿童支气管哮喘有关。我们的数据与其他作者的结果一致。例如,Liu Z.等人揭示了rs1800925 IL13与儿童哮喘发生风险之间的关联,CT和TT基因型在患者组中更为常见。Radhakrishnan A.等对马来西亚成年人群rs1800925 IL13进行了研究,发现患者组T*等位基因频率明显超过对照组该等位基因频率。因此,我们的研究结果表明,IL13 rs1800925多态性与儿童支气管哮喘有关,特别是与其控制水平和疾病严重程度有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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