Association of a single-nucleotide polymorphism in low-density lipoprotein receptor-related protein 5 gene with bone mineral density

被引:70
作者
Urano, T
Shiraki, M
Ezura, Y
Fujita, M
Sekine, E
Hoshino, S
Hosoi, T
Orimo, H
Emi, M
Ouchi, Y
Inoue, S
机构
[1] Univ Tokyo, Grad Sch Med, Dept Geriatr Med, Bunkyo Ku, Tokyo 1138655, Japan
[2] Res Inst & Practice Involut Dis, Nagano, Japan
[3] Nippon Med Coll, Inst Gerontol, Dept Mol Biol, Kawasaki, Kanagawa, Japan
[4] Tokyo Metropolitan Geriatr Med Ctr, Tokyo, Japan
[5] Hlth Sci Univ, Yamanashi, Japan
[6] Saitama Med Sch, Res Ctr Gen Med, Saitama, Japan
关键词
wnt; LRP5; osteoporosis; bone mineral density; polymorphism;
D O I
10.1007/s00774-003-0492-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Low-density lipoprotein receptor-related protein 5 (LRP5) is an important regulator of osteoblast growth and differentiation, affecting peak bone mass in vertebrates. Here, we analyzed whether the LRP5 gene was involved in the etiology of postmenopausal osteoporosis, using association analysis between bone mineral density (BMD) and an LRP5 gene single-nucleotide polymorphism (SNP). Association of an SNP in the LRP5 gene at IVS17-1677C > A (intron 17) with BMD was examined in 308 postmenopausal Japanese women (65.2 +/- 9.6 years; mean +/- SD). The subjects bearing at least one variant A allele (CA + AA; n = 142) had significantly lower Z scores for total body and lumbar BMD than the subjects with no A allele (CC; n = 166) (total body, 0.08 +/- 1.09 versus 0.50 +/- 1.03; P = 0.0022; lumbar spine, -0.42 +/- 1.43 versus -0.02 +/- 1.42; P = 0.013). These findings suggest that the LRP5 gene is a candidate for the genetic determinants of BMD in postmenopausal women, and this SNP could be useful as a genetic marker for predicting the risk of osteoporosis.
引用
收藏
页码:341 / 345
页数:5
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