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首页> 外文期刊>Italian journal of pediatrics >Glutathione S transferase theta1 and mu1 gene polymorphisms and phenotypic expression of asthma in Egyptian children: a case–control study
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Glutathione S transferase theta1 and mu1 gene polymorphisms and phenotypic expression of asthma in Egyptian children: a case–control study

机译:埃及儿童谷胱甘肽S转移酶theta1和mu1基因多态性与哮喘表型表达的病例对照研究

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Background Asthma is the result of a complex interaction between environmental factors and genetic variants that confer susceptibility. The glutathione S-transferases (GSTT1 and GSTM1) are phase II enzymes thought to protect the airways from oxidative stress. Few and contradictory data are available on the association between asthma development and GSTT1 and GSTM1 polymorphisms in different ethnic groups. The current study aimed to investigate whether these polymorphisms are associated with asthma development in the Egyptian population. Methods The cross-sectional study was performed on 94 asthmatic children 6 -12 yrs and 90 matched healthy controls. Candidates were subjected to clinical evaluation and measurement of absolute blood eosinophilic count, total serum IgE, and GSTT1 and GSTM1 genotype by multiplex PCR technique. Results The results for GSTT1 null genotype were 87.2% and 97.2% for asthmatic children and controls respectively and showed to be significantly more in controls (P =0.007, OR:0.683, CI: 0.034 -0.715). The results for GSTM1 null genotype were 50% and 61.1% for asthmatic children and controls respectively and showed to be nonsignificant (p?=?0.130, OR: 1.000, CI: 0.54- 1.86). Also, no association was detected between GSTT1 and GSTM1 polymorphisms and atopic conditions or asthma severity. Conclusion The significant detection of GSTT1 null genotype more in controls than in asthmatics with no association with other atopic manifestations or asthma severity and the lack of association detected between GSTM1 polymorphism in relation to asthma, atopy or asthma severity confirm the uncertain role of those genes in the development of asthma.
机译:背景哮喘是环境因素与遗传易感性之间复杂相互作用的结果。谷胱甘肽S-转移酶(GSTT1和GSTM1)是II期酶,被认为可以保护呼吸道免受氧化应激。关于哮喘发展与不同种族的GSTT1和GSTM1多态性之间的关联的数据很少且相互矛盾。当前的研究旨在调查这些多态性是否与埃及人群的哮喘发展相关。方法对94名6-12岁的哮喘儿童和90名健康对照者进行横断面研究。通过多重PCR技术对候选人进行临床评估,并测量绝对血嗜酸性粒细胞计数,总血清IgE以及GSTT1和GSTM1基因型。结果哮喘儿童和对照组的GSTT1无效基因型结果分别为87.2%和97.2%,并且在对照组中显着更高(P = 0.007,OR:0.683,CI:0.034 -0.715)。对于哮喘儿童和对照,GSTM1无效基因型的结果分别为50%和61.1%,并且显示为无统计学意义(p?=?0.130,OR:1.000,CI:0.54-1.86)。同样,在GSTT1和GSTM1多态性与特应性疾病或哮喘严重程度之间未发现关联。结论对照组GSTT1无效基因型的检出率比哮喘组高,与其他特应性表现或哮喘严重程度无关,且与哮喘,特应性病或哮喘严重程度相关的GSTM1多态性缺乏关联,证实了这些基因在哮喘中的作用不确定。哮喘的发展。

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