| Literature DB >> 14727154 |
Takeshi Mizuguchi1,2, Itsuko Furuta3, Yukio Watanabe1,4, Kazuhiro Tsukamoto2,5, Hiroshi Tomita6, Mitsuhiro Tsujihata7, Tohru Ohta2,8, Tatsuya Kishino2,8, Naomichi Matsumoto1,2, Hisanori Minakami3, Norio Niikawa1,2, Koh-Ichiro Yoshiura9,10.
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.Entities:
Mesh:
Substances:
Year: 2004 PMID: 14727154 DOI: 10.1007/s10038-003-0111-6
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172