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LRP5,即低密度脂蛋白受体相关蛋白5,是骨密度的一个决定因素。

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

作者信息

Mizuguchi Takeshi, Furuta Itsuko, Watanabe Yukio, Tsukamoto Kazuhiro, Tomita Hiroshi, Tsujihata Mitsuhiro, Ohta Tohru, Kishino Tatsuya, Matsumoto Naomichi, Minakami Hisanori, Niikawa Norio, Yoshiura Koh-Ichiro

机构信息

Department of Human Genetics, Graduate School of Biomedical Sciences, Nagasaki University, Sakamoto 1-12-4, Nagasaki 852-8523, Japan.

Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Corporation (JST), Kawaguchi, Japan.

出版信息

J Hum Genet. 2004;49(2):80-86. doi: 10.1007/s10038-003-0111-6. Epub 2004 Jan 15.

Abstract

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.

摘要

骨质疏松症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与九个候选基因(TGFB1、TGFBR2、SMAD2、SMAD3、SMAD4、IFNB1、IFNAR1、FOS和LRP5)之间的关联研究结果,以及一项骨质疏松症的病例对照研究结果。前一项关联研究的样本包括481名日本普通女性。在所检测的九个候选基因中,只有LRP5与BMD显示出显著关联。我们在LRP5内鉴定出一个强连锁不平衡(LD)区域。位于该LD区域的五个LRP5单核苷酸多态性(SNP)中有三个给出了相对显著的结果:在c.2220C>T SNP位点具有C/C基因型的女性与具有C/T和T/T基因型的女性相比,调整后的骨密度(AdjBMD)值更高(p = 0.022);同样,IVS17 - 30G>A位点的G/G基因型女性和c.3989C>T位点的C/C基因型女性分别比具有G/A或A/A基因型(p = 0.039)和C/T或T/T基因型(p = 0.053)的女性显示出更高的AdjBMD。在另一组由126名骨质疏松症患者和131名正常对照组成的样本中进行的病例对照研究,在c.2220C>T位点的等位基因频率也存在显著差异(kappa2 = 6.737,p = 0.009)。这些结果表明,LRP5是骨密度的一个决定因素,并且也与骨质疏松症的风险有关。

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