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[支气管哮喘中性粒细胞表型儿童的支气管高敏反应与谷胱甘肽S-转移酶M1和T1基因多态性]

[Bronchial hypersensitivity in children with the neutrophilic phenotype of bronchial asthma and GSTM1 and GSTT1 gene polymorphism].

作者信息

Bezrukov L A, Koloskova E K, Galushchinskaia A V

出版信息

Klin Med (Mosk). 2014;92(9):51-3.

Abstract

INTRODUCTION

The relationship between bronchial hypersensitivity as the key phenomenon ofbronchial asthma and detoxication GSTM1 or GSTT1 gene polymorphism in children with neutrophilic phenotype of this disease remains unclear

MATERIALS AND METHODS

33 children with bronchial asthma of neutrophile phenotype were examined in histamine and dosed physical exercise (running) tests. In addition GSTM1 and GSTT1 genotyping was performed.

RESULTS

Histamine test revealed bronchial hypersensitivity (HTC < 0.3 mg/ml) in 30.7% of the children with GSTMI and/or GSTTI deletions versus 12.5% of those without deletions (P phi < 0.05). The relative risk ofhypersensitivity to histamine (HTC < 0.3 mg/mI) in the presence of deletions was estimnated as 3.1 (95% CI 1.4-6.4), at OR 2.4 (95% CI 1.08-3.1) andAR = 0.18.

CONCLUSION

Children with the neutrophilic phenotype of bronchial asthma having deletions in the GSTT1/GSTM1 system are characterized by bronchial hypersensitivity to histamine and dosed physical exercises.

摘要

引言

作为支气管哮喘关键现象的支气管高反应性与该疾病嗜中性粒细胞表型儿童的解毒基因GSTM1或GSTT1基因多态性之间的关系仍不清楚。

材料与方法

对33例嗜中性粒细胞表型的支气管哮喘患儿进行组胺和定量体育锻炼(跑步)试验检查。此外,还进行了GSTM1和GSTT1基因分型。

结果

组胺试验显示,GSTMI和/或GSTTI基因缺失的患儿中30.7%存在支气管高反应性(组胺激发浓度<0.3mg/ml),而无基因缺失的患儿中这一比例为12.5%(P<0.05)。存在基因缺失时对组胺高反应性(组胺激发浓度<0.3mg/ml)的相对风险估计为3.1(95%可信区间1.4 - 6.4),比值比为2.4(95%可信区间1.08 - 3.1),归因风险为0.18。

结论

GSTT1/GSTM1系统存在基因缺失的嗜中性粒细胞表型支气管哮喘患儿具有对组胺和定量体育锻炼的支气管高反应性特征。

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