首页> 外文期刊>Archives of medical research >Association Between PPAR-γ and RXR-α Gene Polymorphism and Metabolic Syndrome Risk: A Case-Control Study of a Chinese Han Population
【24h】

Association Between PPAR-γ and RXR-α Gene Polymorphism and Metabolic Syndrome Risk: A Case-Control Study of a Chinese Han Population

机译:PPAR-γ和RXR-α基因多态性与代谢综合征风险的相关性:中国汉族人群的病例对照研究

获取原文
获取原文并翻译 | 示例
           

摘要

Background and Aims: Polymorphisms in peroxisome proliferator activated receptor-γ (PPAR-γ) and retinoid X receptor-α (RXR-α) gene may alter metabolic syndrome (MetS) risks by increasing or decreasing the human adiponectin promoter activity in cells. To test this statement, three potentially functional SNPs of PPAR-γ and four SNPs of RXR-α with minor allele frequency (MAF) ≥0.05 in the Chinese Han population were identified from NCBI dbSNPs database to evaluate their associations with MetS. Methods: TaqMan assay was performed to test the genotypes in MetS patients (n = 901) and normal controls (n = 1009). Serum adiponectin concentration was measured by ELISA kit. Results: The variant genotypes rs2920502CG and CG/CC, rs4240711GG and AG/GG, rs4842194CC and CT/CC, rs3132291CT, CC and CT/CC were associated with MetS. Furthermore, in the haplotype of PPAR-γ gene, compared with the most common haplotype GC, haplotype CC was associated with an increased risk of MetS (crude p = 0.017). In the haplotype of RXR-α gene, haplotype GCGC was associated with a significant protective effect for MetS [adjusted p = 0.002, OR (95% CI) = 0.718 (0.585-0.882)] compared with the most common haplotype GTAT. After taking smoking, alcohol consumption and physical activity as environmental adjustment factors into the analysis, the result showed A1 A2 A4 A5 A6 A7 B1 (rs3856806, rs2920502, rs180128, rs1045570, rs3132291, rs4240711, rs4842194) was the best model (cross-validation consistency 10/10, p = 0.0107). Conclusions: The present study suggested that the variant genotypes in PPAR-γ gene could increase the risk of MetS; however, genotypes in RXR-α gene could decrease the risk of MetS in a Chinese Han population.
机译:背景和目的:过氧化物酶体增殖物激活受体-γ(PPAR-γ)和类维生素A X受体-α(RXR-α)基因的多态性可能通过增加或减少细胞中人脂联素启动子的活性来改变代谢综合征(MetS)的风险。为了检验这一说法,从NCBI dbSNPs数据库中鉴定了中国汉族人群中三个具有潜在等位基因频率(MAF)≥0.05的PPAR-γ潜在功能性SNP和四个RXR-αSNP,以评估它们与MetS的关联。方法:采用TaqMan分析法检测MetS患者(n = 901)和正常对照(n = 1009)的基因型。通过ELISA试剂盒测量血清脂联素浓度。结果:变异基因型rs2920502CG和CG / CC,rs4240711GG和AG / GG,rs4842194CC和CT / CC,rs3132291CT,CC和CT / CC与MetS相关。此外,在PPAR-γ基因的单倍型中,与最常见的单倍型GC相比,单倍型CC与MetS风险增加相关(粗略p = 0.017)。与最常见的单倍型GTAT相比,在RXR-α基因的单倍型中,单倍型GCGC与MetS的显着保护作用相关[校正后的p = 0.002,OR(95%CI)= 0.718(0.585-0.882)]。将吸烟,饮酒和体育锻炼作为环境调节因素进行分析后,结果显示A1 A2 A4 A5 A6 A7 B1(rs3856806,rs2920502,rs180128,rs1045570,rs3132291,rs4240711,rs4842194)是最佳模型(交叉验证)一致性10/10,p = 0.0107)。结论:本研究提示PPAR-γ基因的变异基因型可增加发生MetS的风险。然而,RXR-α基因的基因型可以降低中国汉族人群发生MetS的风险。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号