Research Article

华南地区RXRG单核苷酸多态性与2型糖尿病遗传易感性的关系

卷 20, 期 6, 2020

页: [408 - 414] 页: 7

弟呕挨: 10.2174/1566524020666191206163951

价格: $65

摘要

目的:探讨中国南方汉族人群RXRG rs1467664,rs3753898基因多态性与2型糖尿病遗传易感性的关系。 方法:在我们的病例对照研究中,使用SNPscanTM试剂盒对1092例T2D患者和1092例正常人作为单核苷酸多态性(SNP)rs1467664和rs3753898进行基因分型。用SPSS 20.0软件分析两组的基因型和等位基因频率分布。 结果:RXRG rs3753898的基因型和等位基因的分布在两组之间具有统计学意义,但rs1467664的基因型和等位基因的分布没有显着差异。两组在年龄,性别和体重指数调整前后,rs3753898在加性,显性和隐性模型下均具有统计学意义(P <0.05),但在显性和共显性遗传模型下均未发现统计学差异(P <0.05)。 P> 0.05)。 rs1467664的遗传模型在两组之间没有显着差异(P> 0.05)。由rs1467664等位基因T和rs3753898等位基因A组成的单倍型是T2D的高风险因素,OR = 1.27,95%CI(1.09-1.47),Padj = 0.002。 结论:我们的结果表明,RXRG rs3753898的单核苷酸多态性可能与2型糖尿病的遗传易感性有关。由rs1467664的等位基因T和rs3753898的等位基因A组成的单倍型是2型糖尿病的危险因素,这表明RXRG基因的遗传变异可能是中国汉族人群糖尿病的遗传原因。

关键词: 2型糖尿病(T2D),单核苷酸多态性(SNP),类维生素X受体伽马(RXRG),中国汉族人群。

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