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。

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

摘要

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