...
首页> 外文期刊>The Journal of Urology >The influence of promoter -202 A/C polymorphism (rs2854744) of the IGFBP-3 gene on erectile dysfunction risk and serum levels of IGF-I and IGFBP-3
【24h】

The influence of promoter -202 A/C polymorphism (rs2854744) of the IGFBP-3 gene on erectile dysfunction risk and serum levels of IGF-I and IGFBP-3

机译:IGFBP-3基因启动子-202 A / C多态性(rs2854744)对勃起功能障碍风险和IGF-1和IGFBP-3血清水平的影响

获取原文
获取原文并翻译 | 示例
           

摘要

Purpose: We studied whether the IGFBP-3 gene polymorphism rs2854744 is associated with erectile dysfunction. Materials and Methods: We investigated the association of this polymorphism with erectile dysfunction in 176 cases and 352 controls. We genotyped rs2854744 using polymerase chain reaction-restriction fragment length polymorphism. Circulating concentrations of IGF-I and IGFBP-3 were also measured. Results: Allelic frequencies were 0.474 (A allele) and 0.526 (C allele) in men with erectile dysfunction, and 0.457 (A allele) and 0.543 (C allele) in normal controls (adjusted OR 1.74, 95% CI 0.82-2.43, p = 0.08). The frequency of the IGFBP-3 A-202C polymorphism genotype was 0.273 (CC), 0.506 (AC) and 0.221 (AA) in the case group, and 0.296 (CC), 0.494 (AC) and 0.210 (AA) in the control group (chi-square test p = 0.08). Neither the IGFBP-3 A-202C polymorphism nor serum IGF-I and IGFBP-3 levels were significantly associated with the risk of erectile dysfunction. Carriers of the AA genotype had the highest age adjusted serum IGFBP-3. This demonstrated a stepwise decrease in the presence of 1 or 2 copies of the C allele (mean ?? SD 4,541 ?? 796.2, 3,552 ?? 642.4 and 3,314 ?? 669.3 ng/ml, respectively). There was a positive correlation between serum IGFBP-3 and serum IGF-I concentrations (Spearman correlation coefficient r = 0.34, p for trend = 0.001). Conclusions: The IGFBP-3 gene A-202C polymorphism does not modulate the risk of erectile dysfunction. ? 2013 American Urological Association Education and Research, Inc.
机译:目的:我们研究了IGFBP-3基因多态性rs2854744是否与勃起功能障碍有关。材料和方法:我们调查了176例病例和352例对照者的这种多态性与勃起功能障碍的关系。我们使用聚合酶链反应-限制性片段长度多态性对rs2854744进行基因分型。还测量了IGF-1和IGFBP-3的循环浓度。结果:勃起功能障碍的男性的等位基因频率分别为0.474(A等位基因)和0.526(C等位基因),在正常对照(校正后的OR 1.74,95%CI 0.82-2.43,p)中为0.457(A等位基因)和0.543(C等位基因) = 0.08)。 IGFBP-3 A-202C基因多态性基因型的频率在病例组中为0.273(CC),0.506(AC)和0.221(AA),在对照组中为0.296(CC),0.494(AC)和0.210(AA)组(卡方检验p = 0.08)。 IGFBP-3 A-202C多态性和血清IGF-1和IGFBP-3水平均与勃起功能障碍的风险无显着相关。 AA基因型携带者的年龄调整后的血清IGFBP-3最高。这表明在存在1个或2个拷贝的C等位基因时逐步降低(分别为ΔεSD 4,541Δ796.2、3,552Δ642.4和3,314Δ669.3 ng / ml)。血清IGFBP-3与血清IGF-I浓度呈正相关(Spearman相关系数r = 0.34,趋势p = 0.001)。结论:IGFBP-3基因A-202C多态性不能调节勃起功能障碍的风险。 ? 2013美国泌尿科协会教育与研究公司

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