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TNF-α 启动子多态性与多发性硬化症:-308 和-238 等位基因无关联,但-857 等位基因与土耳其患者的疾病相关。

TNF-alpha promoter polymorphisms in multiple sclerosis: no association with -308 and -238 alleles, but the -857 alleles in associated with the disease in Turkish patients.

机构信息

Department of Neurology, Gaziantep University School of Medicine, Gaziantep, Turkey.

出版信息

Int J Immunogenet. 2010 Apr;37(2):91-5. doi: 10.1111/j.1744-313X.2009.00895.x. Epub 2010 Jan 14.

Abstract

Dysregulation in the expression of pro- and anti-inflammatory cytokines is one of the milestones in multiple sclerosis (MS) development and progression. Tumour necrosis factor (TNF-alpha), a proinflammatory cytokine is believed to play an important role in MS pathogenesis. The objective of this study is to investigate the association between TNF-alpha promoter region (TNF-alpha-238, -308 and -857) and susceptibility to MS and clinical course of the disease. Eighty-six relapsing remitting MS patients and 150 sex-, age- and ethnic-matched controls were enrolled in the study. Genotyping was performed by PCR-RFLP method. We observed a statistically significant increase in TNF-alpha 857 CC genotype in MS patients than controls (P < 0.001) while TNF-alpha 857 CT genotype showed a significant negative correlation with MS patients (P = 0.033). No differences in the distribution of the TNF-alpha-238 and -308 alleles were observed. None of the three polymorphisms (-238, -308 and -857) did not show relation with disease duration, Expanded Disability Status Scale or age of onset. On the other hand, significant difference of TNF -857 CC genotype was identified with the low disease index (P = 0.025). Although the study group is small, the results indicate that TNF-alpha 857 CC genotype may cause susceptibility to MS in the Turkish population.

摘要

细胞因子表达失调是多发性硬化症(MS)发展和进展的里程碑之一。肿瘤坏死因子(TNF-α)是一种促炎细胞因子,被认为在 MS 的发病机制中发挥重要作用。本研究旨在探讨 TNF-α启动子区域(TNF-α-238、-308 和-857)与 MS 的易感性和疾病临床病程之间的关系。研究纳入了 86 例复发缓解型 MS 患者和 150 名性别、年龄和种族匹配的对照者。采用 PCR-RFLP 方法进行基因分型。我们观察到 MS 患者 TNF-α857 CC 基因型的分布显著高于对照组(P<0.001),而 TNF-α857 CT 基因型与 MS 患者呈显著负相关(P=0.033)。TNF-α-238 和-308 等位基因的分布无差异。三个多态性(-238、-308 和-857)均与疾病持续时间、扩展残疾状态量表或发病年龄无关。另一方面,TNF-α-857 CC 基因型与低疾病指数有显著差异(P=0.025)。尽管研究组规模较小,但结果表明,TNF-α857 CC 基因型可能导致土耳其人群易患 MS。

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