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首页> 外文期刊>American Journal of Internal Medicine >Models of Gen-gene Interaction in Determining the Severity of Bronchial Asthma in Children
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Models of Gen-gene Interaction in Determining the Severity of Bronchial Asthma in Children

机译:基因相互作用模型测定儿童支气管哮喘严重程度

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Bronchial asthma (BA) has a polygenic nature, and the onset of its manifestation and features course is realized due to the influence of genetic factors. This study aimed to investigate the effect of polymorphisms of the genes of the phase II detoxification system and genes of the cardiovascular tone on the severity of asthma in children. The study included 163 children aged 5-18 years: 38 with severe asthma, 69 with moderate asthma, and 56 with mild asthma. A molecular genetic study was conducted to determine the frequency of gene propagation and gen-gene interaction by GSTT1, GSTM1, GSTP1, ACE, eNOS, AT2R1, NAT2 genes at different severity of bronchial asthma. Found that in the prediction of the severity of asthma special place belongs to the analysis of the combination of genotypes. Independent effects were found for AT2R1 and ACE gene polymorphisms. The ACE (I / D) / AT2R1 (A1166C) / eNOS (T786C) / eNOS (4b / 4a) four-locus model was developed to predict the severe BA course and the need for additional analysis of the interaction of AT2R1 (A1166C) and eNOS (T786C), eNOS (T786C) genes was demonstrated (4b4a) and GSTT1. The risk of developing severe BA has been demonstrated for the combination of 1166SS + 786TT, 1166CC + 786TC genotypes by AT2R1 (A1166C) and eNOS (T786C) genes, and the reduction of this risk for combinations of eNOS (4b4a) 4b4b + GSTT1 genotypes. In moderate asthma, combinations of ACE genotypes DD + AT2R1 1166SS and AT2R1 313AA + GSTP1 1166SS were reliable risk markers for severe asthma. AT2R1 gene polymorphism was the leading marker in more severe asthma. A marker of severe BA was also found for the heterozygous 857GA polymorphism of the NAT2 gene (G857A). Conclusions. The influence of ACE (I / D), AT2R1 (A1166C), eNOS (T-786C), NAT2 (G857A), GSTT1, and GSTP1 gene polymorphisms on the severity of asthma in children has been established.
机译:支气管哮喘(BA)具有多基因性质,并且由于遗传因素的影响,实现了其表现形式和特征课程的开始。本研究旨在研究II期解毒系统基因的多态性对儿童哮喘哮喘严重程度的影响。该研究包括163例5-18岁的儿童:38例,严重哮喘,69例,中度哮喘,56例,哮喘轻度。进行了分子遗传学研究以确定GSTT1,GSTM1,GSTP1,ACE,ENO,AT2R1,NAT2基因在不同严重程度下的GSTT1,GSTM1,GSTP1,ACE,ENO,NAT2基因的频率。发现,在预测哮喘特殊地区的严重程度属于基因型组合的分析。发现AT2R1和ACE基因多态性的独立效果。开发了ACE(I / D)/ AT2R1(A116C)/ ENOS(4B / 4A)四基因座模型以预测严重的BA课程,并且需要额外分析AT2R1(A1166C)的相互作用和eNOS(t786c),eNOS(t786c)基因被证明(4b4a)和gstt1。通过AT2R1(A1166C)和ENOS(T786C)基因的1166Ss + 786TT,1166CC + 786TC基因型和eNOS(4B4a)4b4b + gstt1基因型的组合的减少。在适度的哮喘中,ACE基因型DD + AT2R1 1166SS和AT2R1 313AA + GSTP1 1166S的组合是严重哮喘的可靠风险标记。 AT2R1基因多态性是在更严重的哮喘中的前导标志物。还发现了NAT2基因的杂合857GA多态性(G857A)的杂合857GA多态性的严重BA的标志物。结论。建立了ACE(I / D),AT2R1(A1166C),eNOS(T-786C),NAT2(G857A),GSTT1和GSTP1基因多态性对儿童哮喘严重程度的影响。

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