Association of estrogen receptor β gene polymorphism with bone mineral density

被引:116
|
作者
Ogawa, S
Hosoi, T
Shiraki, M
Orimo, H
Emi, M
Muramatsu, M
Ouchi, Y
Inoue, S
机构
[1] Tokyo Med & Dent Univ, Fac Med, Dept Geriatr Med, Bunkyo Ku, Tokyo 113, Japan
[2] Tokyo Metropolitan Geriatr Hosp, Itabashi Ku, Tokyo 173, Japan
[3] Res Inst & Practice Involut Dis, Nagano 39981, Japan
[4] Nippon Med Sch, Inst Gerontol, Dept Biol Mol, Nakahara Ku, Kawasaki, Kanagawa 211, Japan
[5] Saitama Med Sch, Dept Biochem, Moroyama, Saitama 35004, Japan
[6] Japan Sci & Technol Corp, CREST, Yokohama, Kanagawa, Japan
关键词
D O I
10.1006/bbrc.2000.2285
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chromosomal mapping of the human estrogen receptor beta (ERP) gene by fluorescence in situ hybridization (FISH) reveals that ERP is located at human chromosome 14, region q23-24.1, where the aberration of DNA copy number in the bone disorders is frequently involved. Then, me investigated the association between dinucleotide (cytosine-adenine; CA) repeat polymorphism located in the flanking region of ERP gene and bone mineral density (BMD) in 204 healthy postmenopausal Japanese women. The genotype was classified into "A" through "O" according to the number of the repeats, from 18 to 32. BMD was expressed in Z score (a deviation from the weight-adjusted average BMD of each age using the standard deviation as a unit). When we separate the subjects into two groups bearing at least one I allele (26 CA repeats) and those who did not, the former subjects had significantly higher Z score of L2-4 BMD (mean +/- standard deviation; 0.674 +/- 1.53 vs 0.128 +/- 1.38; P = 0.027). These data suggest that genetic variation at the ERP locus may be associated with some determinants for BMD and the possible involvements of this polymorphism in the cause of postmenopausal osteoporosis in Japanese women. (C) 2000 Academic Press.
引用
收藏
页码:537 / 541
页数:5
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