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

被引:0
作者
Tomohiko Urano
Masataka Shiraki
Yoichi Ezura
Masayo Fujita
Emiko Sekine
Shinjiro Hoshino
Takayuki Hosoi
Hajime Orimo
Mitsuru Emi
Yasuyoshi Ouchi
Satoshi Inoue
机构
[1] The University of Tokyo,Department of Geriatric Medicine, Graduate School of Medicine
[2] Research Institute and Practice for Involutional Diseases,Department of Molecular Biology, Institute of Gerontology
[3] Nippon Medical School,Research Center for Genomic Medicine
[4] Tokyo Metropolitan Geriatric Medical Center,undefined
[5] Health Science University,undefined
[6] Saitama Medical School,undefined
来源
Journal of Bone and Mineral Metabolism | 2004年 / 22卷
关键词
wnt; LRP5; osteoporosis; bone mineral density; polymorphism;
D O I
暂无
中图分类号
学科分类号
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:4
相关论文
empty
未找到相关数据