伊朗阿塞拜疆多发性硬化症患者中tnf相关凋亡诱导配体受体(TRAIL-R)基因多态性的关联

Bita Amir Taghavi, M. Hashemi, Gholamreza Niaei, S. Rahmani
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引用次数: 1

摘要

简介:多发性硬化症(MS)是一种中枢神经系统慢性炎症性脱髓鞘疾病,伴不同程度的轴突损伤。tnf相关的凋亡诱导配体受体(TRAIL-R)可能在ms的发病机制中发挥重要作用,我们的研究目的是评估位于TRAIL-R1和TRAIL-R2基因的两种常见多态性在ms发病机制中的关联。我们用单链构象多态性(SSCP)对特定区域的两个单核苷酸多态性进行基因分型,并用DNAMAN软件对部分样品的序列结果进行分析。DNA是用盐析法从全血中提取的。采用Pearson’s x2检验分析基因型频率分布。p < 0.05为差异有统计学意义。结果:rs4872077 SNP在PRMS组和PPMS组间无显著差异,rs1001793和rs4872077多态性基因型状态与发病年龄、病程、EDSS无相关性。结论:我们的研究表明,TRAILR多态性与多发性硬化症之间没有关联。然而,这种多态性似乎不是疾病的严重标志,既不能改变MS的临床进展,也不能改变其治疗反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of TNF-related apoptosis inducing ligand receptor (TRAIL-R) gene polymorphisms in Iranian Azeri patients with multiple sclerosis
Introduction: Multiple sclerosis (MS) is a chronic inflammatory demyelinating disorder of the central nervous system with various degrees of axonal damage. The TNF-related apoptosis inducing ligand receptor (TRAIL-R) might be playing an important role in the pathogenesis of MS. The objective of our study was to evaluate the association of two common polymorphisms is located in the TRAIL-R1 and TRAIL-R2 gene, in the pathogenesis of MS. Methods : We genotyped two single nucleotide polymorphisms in particular regions with single strand conformation polymorphism (SSCP) and Results obtained from the sequence of some samples, were analyzed using DNAMAN software. DNA was extracted from whole blood using the salting-out procedure. The distribution of genotype frequencies was analyzed using Pearson’s x 2 test. Statistical significance was defined as p < 0.05. Results: No Significant differences in SNP rs4872077 were found between the PRMS and PPMS groups and No association was found between the genotype status of the rs1001793 and rs4872077 polymorphisms and the age at onset, disease duration, EDSS. Conclusion: Our study suggests no association between TRAILR polymorphisms and MS Disease. Nevertheless, this polymorphisms does not appear to be a severity marker of the disease, neither modifying the clinical progression of MS nor its therapeutic response.
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