...
首页> 外文期刊>Journal of human genetics >LRP5, low-density-lipoprotein-receptor-related protein 5, is a determinant for bone mineral density.
【24h】

LRP5, low-density-lipoprotein-receptor-related protein 5, is a determinant for bone mineral density.

机译:LRP5,低密度脂蛋白受体相关蛋白5,是骨矿物质密度的决定因素。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Osteoporosis is a multifactorial trait with low bone mineral density (BMD). We report results of an association study between BMD and nine candidate genes ( TGFB1, TGFBR2, SMAD2, SMAD3, SMAD4, IFNB1, IFNAR1, FOS and LRP5), as well as of a case-control study of osteoporosis. Samples for the former association study included 481 general Japanese women. Among the nine candidate genes examined, only LRP5 showed a significant association with BMD. We identified a strong linkage disequilibrium (LD) block within LRP5. Of five LPR5 single nucleotide polymorphisms (SNPs) that are located in the LD block, three gave relatively significant results: Women with the C/C genotype at the c.2220C>T SNP site had higher adjusted BMD (AdjBMD) value compared to those with C/T and T/T (p=0.022); and likewise, G/G at IVS17-30G>A and C/C women at c.3989C>T showed higher AdjBMD than those with G/A or A/A (p=0.039) and with C/T or T/T ( p=0.053), respectively. The case-control study in another series of samples consisting of 126 osteoporotic patients and 131 normal controls also gave a significant difference in allele frequency at c.2220C>T (kappa2=6.737, p=0.009). These results suggest that LRP5 is a BMD determinant and also contributes to a risk of osteoporosis.
机译:骨质疏松是一种具有低骨矿物质密度(BMD)的多因素性状。我们报告了BMD与9个候选基因(TGFB1,TGFBR2,SMAD2,SMAD3,SMAD4,IFNB1,IFNAR1,FOS和LRP5)之间的关联研究结果,以及骨质疏松症的病例对照研究。前协会研究的样本包括481名日本普通女性。在检查的九种候选基因中,只有LRP5与BMD显着相关。我们在LRP5中鉴定出一个强连锁不平衡(LD)嵌段。在位于LD区的5个LPR5单核苷酸多态性(SNP)中,有3个产生了相对显着的结果:与C.C基因型位于c.2220C> T SNP位点的女性相比,具有更高的调整BMD(AdjBMD)值C / T和T / T(p = 0.022);同样,IVS17-30G> A的G / G和c.3989C> T的C / C妇女显示的AdjBMD高于G / A或A / A(p = 0.039)和C / T或T / T的妇女。 (p = 0.053)。在由126名骨质疏松症患者和131名正常对照组成的另一系列样本中的病例对照研究也显示,等位基因频率在c.2220C> T时具有显着差异(kappa2 = 6.737,p = 0.009)。这些结果表明,LRP5是BMD的决定因素,也有导致骨质疏松症的风险。

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