Osteoporosis is a common disorder in postmenopausal women, which is pr
obably due to decreased ovarian function. Currently, hormone replaceme
nt therapy (HRT), involving administration of estrogen and progestogen
, is successfully applied to reduce bone resorption. We studied the ef
fect of HRT on 23 postmenopausal women. This consisted of a combinatio
n of 17 beta-estradiol and dydrogesterone, on the serum level of 1,25-
dihydroxyvitamin D (1,25(OH)(2)D) after 0, 6, 12, and 24 months. We fo
und mean serum concentrations (+/-SD) of 1,25(OH)(2)D of 130.5 pmol/li
ter (46.1), 152.7 pmol/liter (45.1), 170.8 pmol/liter (64.0), and 155.
2 pmol/liter (59.7), respectively. The baseline values in these women
were found to be significantly lower than those during therapy (P less
than or equal to 0.005). No statistically significant differences wer
e observed when comparing the estrogen-only phase with the combined es
trogen-progestogen phase. It is concluded that HRT results in an incre
ase in the serum 1,25(OH)(2)D concentration which lasts for at least 2
years. This increase may partly explain the preventive effect of HRT
on osteoporosis. Furthermore, these results suggest that dydrogesteron
e does not influence the estrogen-induced changes in serum 1,25(OH)(2)
D concentration.