首页> 外文期刊>Indian journal of medical sciences. >Tumor necrosis factor - alpha and transforming growth factor - beta1 polymorphisms in bronchial asthma.
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Tumor necrosis factor - alpha and transforming growth factor - beta1 polymorphisms in bronchial asthma.

机译:支气管哮喘中的肿瘤坏死因子-α和转化生长因子-beta1多态性。

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Background: Bronchial asthma is a complex genetic disorder regulated by the release of cytokines and inflammatory mediators. Tumor necrosis factor alpha (TNF-alpha) and transforming growth factor beta (TGF-beta1) cytokines play pivotal roles in the inflammatory response of the airways. Differential production of these two cytokines is associated with allelic variations in the transcriptional regulatory region of these genes. Aims: The objective of the present study was to investigate G-308A TNF-alpha and C-509T TGF- beta1 polymorphisms for their association with Bronchial Asthma. Materials and Methods: DNA isolated from 123 asthmatics and 100 normal healthy controls were screened for these polymorphisms using the amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) methods, developed in our laboratory. Results: Significant allelic association was observed between G-308A TNF-alpha polymorphism and asthma (P = 0.031) while no association was observed with C-509T TGF- beta1 polymorphism (P = 0.207). Further sub-grouping based on either allergic response or family history failed to reveal any statistical significance among the groups or with controls. The interaction between these polymorphisms revealed statistically significant association between the high producer genotype alleles of TNF-alpha and TGF-beta (A/T) and asthma (P = 0.016). Conclusions: The present study reports, for the first time, the role of two polymorphisms, in concert, for their association with asthma in an Indian population. Our study supports the findings that the G-308A TNF-alpha promoter polymorphism is a risk factor for asthma and furthermore suggests that the patients with high producer alleles for TNF-alpha (-308) and TGF-beta (-509) have the highest risk of getting this disease in the Punjabi population.
机译:背景:支气管哮喘是一种复杂的遗传性疾病,受细胞因子和炎性介质释放的调节。肿瘤坏死因子α(TNF-alpha)和转化生长因子β(TGF-beta1)细胞因子在呼吸道的炎症反应中起关键作用。这两种细胞因子的差异产生与这些基因的转录调节区域的等位基因变异有关。目的:本研究的目的是研究G-308ATNF-α和C-509TTGF-β1多态性与支气管哮喘的关系。材料与方法:使用在我们实验室开发的扩增难治性突变系统-聚合酶链反应(ARMS-PCR)方法,对从123名哮喘病患者和100名正常健康对照中分离的DNA进行筛查这些多态性。结果:在G-308ATNF-α多态性与哮喘之间存在显着的等位基因关联(P = 0.031),而与C-509TTGF-β1多态性则没有相关性(P = 0.207)。基于过敏反应或家族病史的进一步分组未能揭示组间或对照组的任何统计学意义。这些多态性之间的相互作用揭示了TNF-α和TGF-β(A / T)的高生产者基因型等位基因与哮喘之间的统计学显着相关性(P = 0.016)。结论:本研究首次报道了两个多态性在印度人人群中与哮喘相关联的作用。我们的研究支持以下发现:G-308ATNF-α启动子多态性是哮喘的危险因素,并且进一步表明,TNF-α(-308)和TGF-beta(-509)产生者等位基因高的患者旁遮普族人群患这种疾病的风险。

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