Kamali-Sarvestani E, Nikseresht A, Aflaki E, Sarvari J, Gharesi-Fard B
Department of Immunology, Faculty of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Acta Neurol Scand. 2007 Mar;115(3):161-6. doi: 10.1111/j.1600-0404.2006.00743.x.
To investigate the association between tumor necrosis factor-alpha (TNF-alpha) G-308A, tumor necrosis factor-beta (TNF-beta) G+252A and interleukin-4 (IL-4) C-590T polymorphisms and susceptibility to multiple sclerosis (MS) development and clinical course of the disease.
Two hundred and seventy patients with MS and 542 sex and ethnic matched controls were enrolled in the present study. An allele-specific oligonucleotide polymerase chain reaction was used to detect the polymorphism at position -308 of the TNF-alpha gene. The genotypes of TNF-beta and IL-4 were determined by polymerase chain reaction-restriction fragment length polymorphism.
Allelic and genotypic frequencies for these polymorphisms were similar in patients with MS and population controls or among different types of the disease.
The results of the present study suggest that the three mentioned functional polymorphisms are not likely to cause susceptibility to MS in the Iranian population.
研究肿瘤坏死因子-α(TNF-α)G-308A、肿瘤坏死因子-β(TNF-β)G+252A和白细胞介素-4(IL-4)C-590T基因多态性与多发性硬化症(MS)发病易感性及疾病临床进程之间的关联。
本研究纳入了270例MS患者以及542例性别和种族匹配的对照。采用等位基因特异性寡核苷酸聚合酶链反应检测TNF-α基因-308位点的多态性。通过聚合酶链反应-限制性片段长度多态性确定TNF-β和IL-4的基因型。
这些多态性的等位基因和基因型频率在MS患者与总体对照之间或不同类型疾病之间相似。
本研究结果表明,上述三种功能性多态性不太可能导致伊朗人群对MS易感。