Polymorphism in the third intron of the interferonγ gene is associated with susceptibility to multiple sclerosis.

X. Wang, F. Meng, X. Wang, S. Wang, L. Guo
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引用次数: 1

Abstract

The present study aims to examine the relationship between polymorphisms in the third intron of the IFN-γ gene and their influence on susceptibility to multiple sclerosis. A population-based case-control study was used for this purpose. Multiple sclerosis patients and healthy controls were interviewed. Genetic polymorphisms of IFN-γ intron III at the +2118 A/G and +3586 G/ACT sites were detected using polymerase chain reaction-restriction fragment length polymorphism. Genotypes and allele frequencies of IFN-γ intron III at the +2118 position were significantly different between multiple sclerosis patients and controls (P ≥ 0.05). However, no difference in allele frequencies was observed at the +3586 position between the two groups (P ≤ 0.05). Thus, polymorphisms at the +2118 A/G site in the IFN-γ intron III gene may be associated with susceptibility to multiple sclerosis.
干扰素γ基因第三个内含子多态性与多发性硬化症易感性相关。
本研究旨在研究IFN-γ基因第三内含子多态性与多发性硬化症易感性的关系。为此目的采用了一项基于人群的病例对照研究。对多发性硬化症患者和健康对照者进行访谈。采用聚合酶链反应-限制性片段长度多态性检测IFN-γ内含子III +2118 A/G和+3586 G/ACT位点的遗传多态性。多发性硬化症患者与对照组IFN-γ内含子III +2118位点基因型及等位基因频率差异有统计学意义(P≥0.05)。两组+3586位点等位基因频率差异无统计学意义(P≤0.05)。因此,IFN-γ内含子III基因+2118 A/G位点的多态性可能与多发性硬化症的易感性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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