B. Ongphiphadhanakul et al., ESTROGEN-RECEPTOR GENE POLYMORPHISM IS ASSOCIATED WITH BONE-MINERAL DENSITY IN PREMENOPAUSAL WOMEN BUT NOT IN POSTMENOPAUSAL WOMEN, Journal of endocrinological investigation, 21(8), 1998, pp. 487-493
In the present study, we examined the genotypes distribution of Pvu II
estrogen receptor (ER) gene polymorphism and its association to bone
mass in Thai females. Subjects consisted of 134 Thai females 54 of who
m were premenopausal and 80 were postmenopausal. Pvu II ER gene polymo
rphism was determined by PCR-RFLP. Capital P represents the absence of
the restriction site while small p indicates the presence of the rest
riction site. Forty nine (36.6%) of the subjects had pp genotype, whil
e 59 (44.0%) had Pp genotype and 26 (19.4%) had PP genotype, There was
no significant difference in age, body weight, height and calcium int
ake in premenopausal women with different genotypes. The results inclu
ding years since menopause were similar in postmenopausal women. When
including ER gene genotypes, age, body weight, height and dietary calc
ium intake in a stepwise multiple regression model, it was found that
besides body weight ER gene polymorphism was associated with bone mine
ral density (BMD) at AP spine (p<0.05), lateral spine (p<0.05) femoral
neck (p<0.05) and femoral trochanter (p<0.05) with the pp genotype ha
ving the least BMD. ER gene polymorphism was the only factor associate
d with BMD at Ward's triangle, (p<0.05) while only body weight was ass
ociated with BMD at distal and mid radius. There was no difference in
serum intact osteocalcin (OC) concentrations among subjects with diffe
rent genotypes. ER gene polymorphism was not related to BMD in postmen
opausal women at any skeletal site. Similarly, serum intact OC levels
were not different among postmenopausal women with different genotypes
. We concluded that Pvu II estrogen receptor gene polymorphism is asso
ciated with bone mineral density in premenopausal women but not in pos
tmenopausal women. Estrogen receptor gene polymorphism may have a modu
latory role in calcium and bone metabolism during adolescence and youn
g adulthood. (J. Endocrinol. Invest. 21: 487-493, 1998) (C) 1998, Edit
rice Kurtis.