SUMY STATE UNIVERSITY, SUMY, UKRAINE.
Pol Merkur Lekarski. 2023;51(4):398-402. doi: 10.36740/Merkur202304115.
Aim: The objective of the study was to evaluate the frequency of the ER22/23EK and Tth111I polymorphic variants in the glucocorticoid receptor (GR) gene in patients with BA and to assess the risk of BA development with regard to these polymorphisms.
Materials and Methods: We examined 553 BA patients and 95 apparently healthy individuals. BA was diagnosed according to the 2016 GINA recommendations and its later versions. The study was approved by the Bioethics Committee of the Medical Institute of Sumy State University. The ER22/23EK (rs 6189/6190) and Tth111I (rs10052957) polymorphisms in the GR gene were determined using polymerase chain reaction-restriction fragment length polymorphism analysis. Statistical analysis of obtained results was performed using SPSS-17 program.
Results: The obtained distribution of genotypes for the ER22/23EK and Tth111I polymorphisms in the GR gene corresponded to the Hardy-Weinberg expectations (p > 0.05). We revealed no significant difference in the distribution of alleles and genotypes for the ER22/23EK polymorphism in the GR gene in patients with asthma and apparently healthy individuals (χ2 = 4.14; p = 0.126); apart from that, we found no statistically significant association with BA risk in any model of inheritance. A statistically significant difference was observed in the distribution of genotypes for the Tth111I polymorphism in the GR gene in patients with asthma and apparently healthy individuals (χ2 = 6.278; p = 0.043). BA risk was 2.69 times higher in the carriers of TT genotype for the Tth111I polymorphism in the GR gene vs. major allele carriers. No gender-specific difference was observed in the distribution of genotypes and alleles for the ER22/23EK and Tth111I polymorphisms in the GR gene.
Conclusions: We found no gender-specific difference in the distribution of alleles and genotypes for the ER22/23EK and Tth111I polymorphisms in the GR gene; no difference in the distribution of alleles and genotypes for the ER22/23EK polymorphism in the GR gene in patients with asthma and apparently healthy individuals; and no statistically significant association with BA risk. A statistically significant difference was observed in the distribution of genotypes for the Tth111I polymorphism in the GR gene in patients with asthma and apparently healthy individuals; also, BA risk was 2.69 times higher in the minor allele homozygous patients vs. major allele carriers.
本研究旨在评估糖皮质激素受体(GR)基因中 ER22/23EK 和 Tth111I 多态性在 BA 患者中的频率,并评估这些多态性与 BA 发展风险的关系。
我们检查了 553 名 BA 患者和 95 名貌似健康的个体。BA 根据 2016 年 GINA 建议及其后续版本进行诊断。该研究得到了苏梅州立大学医学研究所生物伦理委员会的批准。使用聚合酶链反应-限制性片段长度多态性分析确定 GR 基因中的 ER22/23EK(rs6189/6190)和 Tth111I(rs10052957)多态性。使用 SPSS-17 程序对获得的结果进行统计分析。
GR 基因中 ER22/23EK 和 Tth111I 多态性的基因型分布与 Hardy-Weinberg 期望相符(p>0.05)。我们发现哮喘患者和貌似健康个体中 GR 基因 ER22/23EK 多态性的等位基因和基因型分布无显著差异(χ2=4.14;p=0.126);此外,我们在任何遗传模型中均未发现与 BA 风险有统计学意义的关联。GR 基因 Tth111I 多态性的基因型分布在哮喘患者和貌似健康个体之间存在统计学显著差异(χ2=6.278;p=0.043)。与主要等位基因携带者相比,GR 基因 Tth111I 多态性 TT 基因型携带者的 BA 风险高 2.69 倍。GR 基因 ER22/23EK 和 Tth111I 多态性的基因型和等位基因在性别之间无差异。
我们发现 GR 基因中 ER22/23EK 和 Tth111I 多态性的等位基因和基因型在性别之间无差异;GR 基因 ER22/23EK 多态性在哮喘患者和貌似健康个体中的等位基因和基因型分布无差异;与 BA 风险无统计学意义的关联。GR 基因 Tth111I 多态性的基因型分布在哮喘患者和貌似健康个体之间存在统计学显著差异;与主要等位基因携带者相比,GR 基因 Tth111I 多态性 TT 基因型携带者的 BA 风险高 2.69 倍。