考虑发病年龄,β2-腺苷酸受体基因 GLN27GLU 多态性变异体决定的肥胖相关性抽搐症临床过程

V. Kachkovska, L. N. Prystupa
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The control group consisted of 95 practically healthy people. Patients were divided into two clinical groups depending on the age of onset of BA: the first group included 100 patients with an early onset, the second group - 95 patients with a late onset.  The diagnosis and treatment of asthma followed the guidelines of the Global Initiative for Asthma (2016) and its updated versions. The study was approved by the Bioethics Commission of the Educational and Scientific Medical Institute of Sumy State University. Determination of the Gln27Glu polymorphism of the β2-AR gene (rs1042714) was performed using the polymerase chain reaction with the subsequent analysis of restriction fragments. Statistical analysis of the obtained results was carried out using the SPSS-17 program. Pearson's chi-squared test was used to compare genotype distributions between experimental groups. 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引用次数: 0

摘要

导言。研究表明,与肥胖相关的支气管哮喘(BA)病程更长,控制率更低,基本治疗效果不佳的病例更多,病情加重的情况也更频繁。根据发病年龄,支气管哮喘与肥胖合并症可分为两种表型:早期特应性和晚期非特应性。众所周知,与 β2-肾上腺素受体(AR)基因相关的遗传因素对哮喘和肥胖的发病都很重要。本研究旨在分析 β2-肾上腺素受体基因 Gln27Glu 多态性与支气管哮喘合并肥胖病程严重程度的关系,同时考虑到发病年龄。研究材料和方法。研究人员对 195 名同意参与研究的肥胖症哮喘患者进行了调查。对照组由 95 名身体健康的人组成。根据哮喘病的发病年龄,患者被分为两个临床组:第一组包括 100 名发病较早的患者,第二组--95 名发病较晚的患者。 哮喘的诊断和治疗遵循《全球哮喘倡议》(2016 年)及其更新版本的指南。该研究获得了苏美州立大学教育与科学医学院生物伦理委员会的批准。β2-AR基因的Gln27Glu多态性(rs1042714)是通过聚合酶链反应和随后的限制性片段分析确定的。使用 SPSS-17 程序对所得结果进行了统计分析。皮尔逊卡方检验用于比较实验组之间的基因型分布。为了确定 BA 和肥胖的风险,计算了显性、隐性、超显性和加性遗传模式的几率比和 95% 的置信区间。其相关性使用 Akaike 信息标准进行评估。所有检验均为双侧检验,P < 0.05 的值被认为具有统计学意义。研究结果在早发肥胖相关性哮喘患者中,根据β2-AR基因的Gln27Glu多态性,Gln/Gln、Gln/Glu和Glu/Glu基因型的频率分别为70.0;25.0;5.0%的患者病程较轻,55.0%的患者病程较重,36.2%的患者病程较轻,8.8%的患者病程较重(χ2 = 1.49;P = 0.473);而晚期发病的患者病程较轻,50.0%的患者病程较轻,43.8%的患者病程较重,6.2%的患者病程较轻,54.0%的患者病程较轻,31.7%的患者病程较重,14.3%的患者病程较重(χ2 = 2.10;P = 0.350)。尽管病程严重程度不同,基因型的分布可能没有差异,但研究发现,与轻度 BA 病程的患者相比,早期 BA 病程严重的患者小等位基因的同卵双生率是后者的 1.8 倍,晚期 BA 的同卵双生率是后者的 2.3 倍。在所有遗传模型中,肥胖和严重病程的早发型 BA 风险均无关联,而在加性遗传模型中,晚发型 BA 患者的风险增加了 1.66 倍(95% CI (1.03 - 2.72),p = 0.04)(p = 0.04)。结论β2-AR基因Gln27Glu多态性的基因型分布与肥胖症早期和晚期BA病程的严重程度没有明显的统计学差异。早期 BA 病程严重的风险与 β2-AR基因的 Gln27Glu 多态性无关,而晚期 BA 在加性遗传模型中增加了 1.66 倍。
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CLINICAL COURSE OF OBESITY-ASSOCIATED ASTHMA DEPENDING ON THE GLN27GLU POLYMORPHIC VARIANT OF THE β2-ADRENORECEPTOR GENE, TAKING INTO ACCOUNT THE AGE OF ONSET
Introduction. Studies have shown that bronchial asthma (BA) associated with obesity has a more severe course, lower control, more frequent cases of low efficacy of basic treatment, and exacerbations. Two phenotypes have been distinguished in BA-obesity comorbidity based on age of onset: early atopic and late non-atopic. It is known that genetic factors associated with β2-adrenoceptor (AR) genes are important in the development of both asthma and obesity. The purpose of the study aimed to analyze the association of the Gln27Glu polymorphism of the β2-adrenoceptor gene with the severity of the course of bronchial asthma with obesity, taking into account the age of its onset. Research material and methods. 195 asthma patients with obesity consented for the study participation were examined. The control group consisted of 95 practically healthy people. Patients were divided into two clinical groups depending on the age of onset of BA: the first group included 100 patients with an early onset, the second group - 95 patients with a late onset.  The diagnosis and treatment of asthma followed the guidelines of the Global Initiative for Asthma (2016) and its updated versions. The study was approved by the Bioethics Commission of the Educational and Scientific Medical Institute of Sumy State University. Determination of the Gln27Glu polymorphism of the β2-AR gene (rs1042714) was performed using the polymerase chain reaction with the subsequent analysis of restriction fragments. Statistical analysis of the obtained results was carried out using the SPSS-17 program. Pearson's chi-squared test was used to compare genotype distributions between experimental groups. To determine the risk of BA and obesity, odds ratios and 95% confidence intervals were calculated for dominant, recessive, superdominant, and additive models of inheritance. Their relevance was assessed using the Akaike information criterion. All tests were two-sided, and values p < 0.05 were considered statistically significant. Research results. The frequency of Gln/Gln, Gln/Glu and Glu/Glu genotypes according to the Gln27Glu polymorphism of the β2-AR gene in patients with early-onset obesity-associated asthma was 70.0; 25.0; 5.0% with a mild course and 55.0; 36.2; 8.8% with severe (χ2 = 1.49; p = 0.473); and with a late debut - 50.0; 43.8; 6.2% with mild and 54.0%; 31.7; 14.3%, respectively, with severe (χ2 = 2.10; p = 0.350). Despite the absence of a probable difference in the distribution of genotypes depending on the severity of the course, it was found that the frequency of homozygotes for the minor allele was 1.8 times higher in patients with a severe course of early BA and 2.3 times higher in late BA compared to that in patients with mild BA course. The risk of early-onset BA with obesity and a severe course showed no association in all models of inheritance, and in patients with late-onset BA, there was a 1.66-fold increase (95% CI (1.03 – 2.72), p = 0.04) in the additive inheritance model (p = 0.04). Conclusions. There are no statistically significant differences in the distribution of genotypes according to the Gln27Glu polymorphism of the β2-AR gene depending on the severity of the course of early and late BA with obesity. The risk of developing a severe course of early BA did not depend on the Gln27Glu polymorphism of the β2-AR gene, and late BA increased by 1.66 times in the additive model of inheritance.
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