首页> 外文期刊>Biotechnology & Biotechnological Equipment >THE TUMOR NECROSIS FACTOR-A -308 G/A POLYMORPHISM AND THE TUMOR NECROSIS FACTOR-RELATED APOPTOSIS-INDUCING LIGAND POLYMORPHISMS, IN ASTHMATIC PATIENTS AND HEALTHY SUBJECTS
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THE TUMOR NECROSIS FACTOR-A -308 G/A POLYMORPHISM AND THE TUMOR NECROSIS FACTOR-RELATED APOPTOSIS-INDUCING LIGAND POLYMORPHISMS, IN ASTHMATIC PATIENTS AND HEALTHY SUBJECTS

机译:哮喘患者和健康受试者的肿瘤坏死因子-A -308 G / A多态性和肿瘤坏死因子诱导的凋亡多态性

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摘要

Asthma is a chronic inflammatory disorder of the airways in which many cells and cellular elements play a role. Like other atopic diseases, asthma is a complex disorder caused by interactions between multiple genes of small to modest effect and equally important environmental factors. The aim of this study was to determine the TNF- alpha -308 G/A polymorphism and the TRAIL polymorphisms, and their influence on asthma in asthmatic patients and healthy subjects. The study population consists of 51 asthmatic patients (47 female and 4 male) and 72 healthy subjects (62 female and 10 male). The mean age of the asthmatic patients and healthy controls were 45.33 plus or minus 14.05, and 41.88 plus or minus 17.41 years, respectively. The asthmatic patients and healthy controls were similar with respect to their ages and sex characters. There was statistically a significant difference between the asthmatic patients and control groups in terms of TRAIL Arg141His, G422A (rs6557634) polymorphism (p=0.02). Statistically, there was not any significant difference between the asthmatic patients and control groups for TRAIL Thr209Arg, C626G (rs20575) TRAIL Glu228Ala, A683C (rs20576) and polymorphisms (p=0.57). Also, there was no significant difference between the asthmatic patients and control groups in terms of TNF- alpha -308 G/A polymorphism (p=0.90). In our study, the TRAIL Arg141His G422A (rs6557634) polymorphism was detected for the first time in asthmatic patients, which may influence the susceptibility to the asthma.
机译:哮喘是气道的慢性炎性疾病,许多细胞和细胞成分在其中起作用。像其他特应性疾病一样,哮喘是一种复杂的疾病,由多种影响较小或中等的基因与同等重要的环境因素相互作用而引起。这项研究的目的是确定TNF-α-308 G / A多态性和TRAIL多态性,及其对哮喘患者和健康受试者哮喘的影响。该研究人群包括51位哮喘患者(47位女性和4位男性)和72位健康受试者(62位女性和10位男性)。哮喘患者和健康对照组的平均年龄分别为正负14.05岁的45.33岁和正负17.41岁的41.88岁。哮喘患者和健康对照者的年龄和性别特征相似。就TRAIL Arg141His,G422A(rs6557634)多态性而言,哮喘患者和对照组之间在统计学上有显着差异(p = 0.02)。统计学上,哮喘患者和对照组在TRAIL Thr209Arg,C626G(rs20575)TRAIL Glu228Ala,A683C(rs20576)和多态性之间无显着差异(p = 0.57)。同样,哮喘患者和对照组在TNF-α-308 G / A多态性方面也没有显着差异(p = 0.90)。在我们的研究中,首次在哮喘患者中检测到TRAIL Arg141His G422A(rs6557634)多态性,这可能会影响对哮喘的易感性。

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