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TNF-α and TNF-β Gene Polymorphism in Saudi Rheumatoid Arthritis Patients

机译:沙特类风湿关节炎患者的TNF-α和TNF-β基因多态性

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Background: Tumor necrosis factor (TNF)-α and -β are cytokines with a wide range of inflammatory, apoptotic and immunomodulatory activities. TNF-α promoter –308 G < A polymorphism has been reported to be associated with rheumatoid arthritis (RA) with inconsistent results.Objective: The aim of this study is to elucidate a possible association of TNF-α (G–308A) and TNF-β (A+252G) polymorphisms with the susceptibility of RA in Saudi patients.Patients and methods: This case control study consisted of 232 Saudi subjects including 106 RA patients and 126 matched controls. Genomic DNA was extracted using QIAampR DNA mini kit (Qiagen CA, USA). TNF-α and TNF-β genes were amplified using Arms primers.Results: The frequencies of TNF-α (–308) allele G and genotype GG were significantly higher in RA patients as compared to controls while allele A and genotype AA were predominant in control group. On the other hand the frequency of TNF-β (+252) GG and AA genotypes were significantly higher in RA patients as compared to controls while GA genotype was predominant in controls. It was inferred that genotype GG positive individuals at position -308 of TNF-α were susceptible to RA while genotype AA might has a protective effect on RA susceptibility in Saudis. Whereas GG and AA genotype of TNF-β at +252 position might exert additive susceptibility to RA and GA might be refractory. However, there was no significant association between duration of morning stiffness, RF positivity and number of joints involved and distribution of alleles/genotypes of TNF-α (-308) or TNF-β (+252) polymorphism. It may be concluded that the TNF-α (?308) and TNF-β (+252) polymorphisms might influence the susceptibility to RA in Saudi population. These results might have prognostic value for future clinical observations.
机译:背景:肿瘤坏死因子(TNF)-α和-β是具有广泛的炎症,凋亡和免疫调节活性的细胞因子。 TNF-α启动子–308 G <据报道,多态性与类风湿关节炎(RA)相关,结果不一致。目的:本研究的目的是阐明TNF-α(G–308A)与TNF的可能关联。 -β(A + 252G)多态性与沙特阿拉伯患者的RA易感性。患者和方法:本病例对照研究包括232名沙特阿拉伯受试者,包括106名RA患者和126名相匹配的对照。使用QIAampR DNA mini试剂盒(美国加利福尼亚州Qiagen)提取基因组DNA。结果:RA患者的TNF-α(–308)等位基因G和基因型GG的频率显着高于对照组,而等位基因A和基因型AA占主导地位。控制组。另一方面,与对照组相比,RA患者的TNF-β(+252)GG和AA基因型频率明显高于对照组,而GA基因型在对照组中占主导地位。可以推断,TNF-α-308位的GG基因型阳性个体易患RA,而AA基因型可能对沙特阿拉伯的RA易感性具有保护作用。而在+252位的GG和AA基因型的TNF-β可能对RA产生加和敏感性,而GA可能是难治性的。然而,早晨僵硬的持续时间,RF阳性与所涉及的关节数量与TNF-α(-308)或TNF-β(+252)多态性等位基因/基因型分布之间没有显着关联。可以得出结论,TNF-α(?308)和TNF-β(+252)多态性可能影响沙特人群对RA的易感性。这些结果可能对将来的临床观察具有预后价值。

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