Investigation of the Association between rs2296283 and rs7337610 Polymorphisms of FLT-1 Gene with Behcet’s Disease in the Population of Tehran-Iran

Z. Bakhshi, Z. Amiri, M. Karimipoor, R. Shokri
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Abstract

Background: Behcet’s Disease (BD) is a rare autoimmune disease with undetermined etiology. In this study, the association of rs2296283 and rs7337610 polymorphisms of FLT-1 gene with the possibility for BD was investigated in Tehran population. Methods: In this case-control study, 100 samples (50 patients with BD and 50 healthy individuals with no background of disease) were examined. PCR-RFLP procedure was performed to determine the rs2296283 and rs7337610 polymorphisms using the HaeIII and MseI enzymes, respectively. SNPStats software was used for the analysis of association study. Results: The frequencies of CC, CT, and TT genotypes for rs2296283 polymorphism were 26, 35, and 39% in patients, and 32, 34, and 34% in healthy population, respectively (p>0.05). The frequency of TT, CT and CC genotypes for FLT-1 rs7337610 polymorphism in patients with BD was 18%, 31%, 51% and in healthy or control groups was 14%, 36% and 50%, respectively (p>0.05). Conclusion: No significant relationship was observed between rs2296283 and rs7337610 polymorphisms and the BD. Study on a greater number of samples is proposed.
伊朗德黑兰人群FLT-1基因rs2296283和rs7337610多态性与白塞病的相关性研究
背景:白塞氏病(BD)是一种罕见的自身免疫性疾病,病因不明。本研究在德黑兰人群中研究了FLT-1基因rs2296283和rs7337610多态性与BD可能性的关系。方法:在本病例对照研究中,检测了100例样本(50例BD患者和50例无疾病背景的健康个体)。利用HaeIII酶和MseI酶对rs2296283和rs7337610基因进行PCR-RFLP分析。采用SNPStats软件进行关联研究分析。结果:rs2296283多态性CC、CT、TT基因型在患者中的频率分别为26、35、39%,在健康人群中的频率分别为32、34、34% (p>0.05)。BD患者中FLT-1 rs7337610多态性出现TT、CT和CC基因型的频率分别为18%、31%和51%,健康组和对照组分别为14%、36%和50% (p>0.05)。结论:rs2296283和rs7337610多态性与BD无显著关系,建议开展更大样本的研究。
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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