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儿童支气管高反应性的分子遗传学方面——放射性污染地区的居民。

MOLECULAR GENETIC ASPECTS OF BRONCHIAL HYPERREACTIVITY IN CHILDREN - RESIDENTS OF RADIOACTIVELY CONTAMINATED AREAS.

机构信息

State Institution «National Research Center for Radiation Medicine of the National Academy of Medical Sciences of Ukraine», 53 Yuriia Illienka St., Kyiv, 04050, Ukraine.

出版信息

Probl Radiac Med Radiobiol. 2020 Dec;25:531-542. doi: 10.33145/2304-8336-2020-25-531-542.

Abstract

OBJECTIVE

to determine the relationship between polymorphisms of glutathione S-transferase gene family andbronchial hyperreactivity in children living in radioactively contaminated areas.

MATERIALS AND METHODS

School age children-residents of radioactively contaminated areas (RCA), without clinicalsigns of respiratory pathology were examined. Molecular genetic studies were carried out by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) for further analysis. The GSTT1, GSTM1 gene deletion polymorphism was investigated using multiplex PCR. PCR and PCR-RFLP analyses were performed in the studyof the GSTP1 gene A313G polymorphism. The ventilation lung capacity was examined by the pneumotachographicmethod according to the analysis of «the flow-volume» loop. The pharmacologic inhalation test with bronchodilator drug, affecting the β2-adrenergic lung receptors was used to detect the early changes in the ventilation lungcapacity - the bronchial hyperreactivity (latent and nonlatent bronchospasm).

RESULTS

Molecular genetic studies showed that the GSTM1 gene deletion genotype and the GSTP1 gene A313G polymorphism were found significantly more often in the subgroup of children with bronchial hyperreactivity living inRCA than in children without bronchial hyperreactivity and children of the control group. The frequency of GSTT1deletion polymorphism did not have a statistically significant difference in all subgroups.

CONCLUSIONS

The GSTM1 gene deletion polymorphism and the GSTP1 gene A313G genotype may be a risk factor fordeveloping bronchial hyperreactivity in children living under adverse environmental conditions, including radioactively contaminated areas.

摘要

目的

确定谷胱甘肽 S-转移酶基因家族多态性与生活在放射性污染地区儿童的支气管高反应性之间的关系。

材料和方法

检查了来自放射性污染地区(RCA)的学龄儿童,这些儿童没有呼吸道病理的临床症状。通过聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)进行分子遗传学研究,以进行进一步分析。使用多重 PCR 研究 GSTT1、GSTM1 基因缺失多态性。进行了 GSTP1 基因 A313G 多态性的 PCR 和 PCR-RFLP 分析。采用呼吸流速法检查通气肺容量。使用影响β2-肾上腺素能肺受体的支气管扩张药物进行药理吸入试验,以检测通气肺容量的早期变化 - 支气管高反应性(潜伏性和非潜伏性支气管痉挛)。

结果

分子遗传学研究表明,与没有支气管高反应性的儿童和对照组儿童相比,生活在 RCA 的支气管高反应性儿童亚组中更频繁地发现 GSTM1 基因缺失基因型和 GSTP1 基因 A313G 多态性。GSTT1 缺失多态性的频率在所有亚组中均无统计学差异。

结论

GSTM1 基因缺失多态性和 GSTP1 基因 A313G 基因型可能是儿童在包括放射性污染地区在内的不利环境条件下发展支气管高反应性的危险因素。

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