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

被引:0
作者
Takeshi Mizuguchi
Itsuko Furuta
Yukio Watanabe
Kazuhiro Tsukamoto
Hiroshi Tomita
Mitsuhiro Tsujihata
Tohru Ohta
Tatsuya Kishino
Naomichi Matsumoto
Hisanori Minakami
Norio Niikawa
Koh-ichiro Yoshiura
机构
[1] Nagasaki University,Department of Human Genetics, Graduate School of Biomedical Sciences
[2] Japan Science and Technology Corporation (JST),Core Research for Evolutional Science and Technology (CREST)
[3] Asahikawa Medical College,Department of Obstetrics and Gynecology
[4] Hokkaido University,Department of Obstetrics and Gynecology, Graduate School of Medicine
[5] Nagasaki University,Department of Clinical Pharmacy, Graduate School of Biomedical Sciences
[6] Nagasaki Prefectural Medical Health Center,Division of Functional Genomics, Center for Frontier Life Sciences
[7] Nagasaki Kita Hospital,undefined
[8] Nagasaki University,undefined
来源
Journal of Human Genetics | 2004年 / 49卷
关键词
Bone mineral density; Osteoporosis; Association study; Haplotype analysis; LRP5;
D O I
暂无
中图分类号
学科分类号
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 (ϰ2=6.737, p=0.009). These results suggest that LRP5 is a BMD determinant and also contributes to a risk of osteoporosis.
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页码:80 / 86
页数:6
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