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肿瘤坏死因子-α 基因-308G/A 多态性与复发性缓解型多发性硬化患者 TNF-α 血清水平的关系。

Association of polymorphism -308G/A in tumor necrosis factor-alpha gene () and TNF-α serum levels in patients with relapsing-remitting multiple sclerosis.

机构信息

Department of Molecular Biology, Immunology and Medical Genetics, Medical Faculty, Trakia University, Stara Zagora, Bulgaria.

Department of Neurology, Faculty of Medicine, Medical University of Plovdiv, Plovdiv, Bulgaria.

出版信息

Neurol Res. 2021 Apr;43(4):291-298. doi: 10.1080/01616412.2020.1853987. Epub 2020 Nov 30.

DOI:10.1080/01616412.2020.1853987
PMID:33252003
Abstract

TNF-α is an important cytokine of the inflammatory response involved in the pathogenesis of relapsing-remitting multiple sclerosis (RRMS). The aim of this study is to explore the association between the promoter polymorphism -308G/A in the gene (rs1800629) with genetic susceptibility to RRMS.: A group of 183 RRMS patients and 169 age and gender-matched healthy controls were enrolled in the study. Genotyping of the polymorphism was performed by PCR-restriction fragment length polymorphism and quantification of TNF-α serum levels was conducted by ELISA.: The genotype distribution in female patients showed a significantly elevated frequency of heterozygotes (AG) (23.5% vs. 12.8%, OR = 2.072, p = 0.029) in comparison with the healthy women. Substantially higher TNF-α serum levels were observed in females compared to males, in both patients and healthy controls (p < 0.05). According to the genotype, TNF-α levels in the RRMS group were calculated in the following order: for GA/AA genotypes (5.67pg/ml vs. 3.48pg/ml, p = 0.0031) and for GG genotypes (4.58pg/ml vs. 3.52pg/ml, p = 0.00043). Moreover, the carriers of at least one A-allele of -308G/A polymorphism (GA+AA) are significantly associated with two fold increased risk for RRMS development (OR = 1.950; p = 0.042) in women in contrast to men as well as associated with early onset of the disease (OR = 2.400; p = 0.021).: Our study showed that the level of TNF-α in the serum of patients with RRMS showed a significant association with the -308G/A polymorphism and gender dependency.

摘要

肿瘤坏死因子-α(TNF-α)是炎症反应中的一种重要细胞因子,参与复发缓解型多发性硬化症(RRMS)的发病机制。本研究旨在探讨基因(rs1800629)启动子多态性-308G/A 与 RRMS 遗传易感性的关系。

方法

纳入了 183 例 RRMS 患者和 169 名年龄和性别匹配的健康对照者。通过 PCR-限制性片段长度多态性分析对多态性进行基因分型,并通过 ELISA 定量检测 TNF-α 血清水平。

结果

在女性患者中,杂合子(AG)的基因型分布频率明显升高(23.5% vs. 12.8%,OR=2.072,p=0.029),与健康女性相比。与男性相比,女性患者和健康对照者的 TNF-α 血清水平均明显升高(p<0.05)。根据基因型,RRMS 组的 TNF-α 水平计算结果如下:GA/AA 基因型组(5.67pg/ml vs. 3.48pg/ml,p=0.0031)和 GG 基因型组(4.58pg/ml vs. 3.52pg/ml,p=0.00043)。此外,-308G/A 多态性(GA+AA)至少携带一个 A 等位基因的携带者发生 RRMS 的风险显著增加两倍(OR=1.950;p=0.042),在女性中与男性相比,并且与疾病的早发有关(OR=2.400;p=0.021)。

结论

我们的研究表明,RRMS 患者血清 TNF-α水平与-308G/A 多态性和性别依赖性有显著关联。

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