Association of bone mineral density with polymorphism of the estrogen receptor gene

• Published in: Journal of bone and mineral research 1996-03, Vol.11 (3), p.306-311
• Main Authors: Kobayashi, Shinji, Inoue, Satoshi, Hosoi, Takayuki, Ouchi, Yasuyoshi, Shiraki, Masataka, Orimo, Hajime
• Format: Article
• Language: English
• Subjects: Aged; Aged, 80 and over; Base Sequence; Biological and medical sciences; Bone Density - genetics; Chromatography, High Pressure Liquid; Diseases of the osteoarticular system; DNA - chemistry; DNA - genetics; Female; Gene Expression Regulation - genetics; Genotype; Humans; Japan; Lumbar Vertebrae - physiology; Medical sciences; Middle Aged; Molecular Sequence Data; Osteoporosis, Postmenopausal - genetics; Osteoporosis. Osteomalacia. Paget disease; Polymorphism, Genetic - genetics; Polymorphism, Restriction Fragment Length; Receptors, Estrogen - genetics
• ISSN: 0884-0431; 1523-4681
• DOI: 10.1002/jbmr.5650110304

PvuII and XbaI restriction fragment length polymorphisms (RFLPs) of the estrogen receptor (ER) gene and its relation to bone mineral density (BMD) were examined in 238 postmenopausal healthy women aged 45–91 years (66.3 ± 0.6 years, mean ± standard error of the mean [SEM]) in Japan. The RFLPs were represented as Pp (PvuII) and Xx (XbaI), with capital letters signifying the absence of and small letters the presence of restriction sites. In the PPxx genotype (n = 18), Z score values of BMD were significantly lower than those for other genotypes (n = 220) (lumbar spine, −0.746 vs. −0.065 [p = 0.022]; total body, −0.482 vs. 0.308 [p = 0.002]). We classified the subjects into three genotypes with allelic haplotype: homozygote of the Px haplotype was expressed as the 11 genotype, heterozygote of the Px haplotype as the 10 genotype, and the one lacking the Px haplotype as the 00 genotype. The PpXx genotype was not included in this analysis because the allelic haplotypes are uncertain. The Px haplotype was associated with a low BMD in postmenopausal women (Z score for the lumbar spine, −0.746 vs. −0.279 vs. 0.083, for the 11, 10, 00 genotypes, respectively [p = 0.029]; Z score for the total body, −0.482 vs. 0.164 vs. 0.427, respectively [p = 0.003]). We suggest that some variation of the ER gene linked to these RFLPs is associated with low BMD and that this at least partly explains the cause of postmenopausal osteoporosis in Japanese women.