Effect of transdermal l7?-estradiol and oral conjugated equine estrogens on biochemical parameters of bone resorption in natural menopause
- 1 July 1993
- journal article
- clinical trial
- Published by Springer Nature in Calcified Tissue International
- Vol. 53 (1) , 13-16
- https://doi.org/10.1007/bf01352008
Abstract
Objective: To evaluate and compare the effects or oral and transdermal estrogen replacement therapy on biochemical markers of bone resorption in early postmenopausal women Design: Controlled, randomized group comparison. Setting: Outpatient clinic for menopausal women and research into osteoporosis. Subjects: Sixty healthy women menopausal for less than 5 years and who had never received any medications interfering with bone metabolism. Interventions: The 60 women were randomly allocated to 3 months therapy with either oral conjugated estrogens (0.625 mg/day) (n = 28) or transdermal estradiol (50 jig/day) (n = 32) in cyclical combination with medroxyprogesterone acetate (5 mg/day). Main outcome measures: Traditional (urinary calcium/creatinine and hydroxyproline/creatinine) and the new specific (urinary pyridinoline/creatinine and deoxypyridinoline/creatinine) markers of bone resorption were determined before and after 3 months of treatment. Results: In both groups, circulating levels of estrone and estradiol were significantly (P < 0.001) increased during treatment. In women treated with oral conjugated equine estrogens, urinary calcium/creatinine and hydroxyproline/creatinine ratios were significantly (P < 0.05) reduced. Pyridinoline/creatinine ratio fell from 69.1 (4) [mean (SEM)] to 50 (4) μmol/μmol (P < 0.01) and deoxypyridinoline/creatinine ratio fell from 10.8 (1) [mean (SEM)] to 8.3 (0.8) μmol/μmol (P < 0.01). In the group treated with transdermal estradiol, urinary hydroxyproline/creatinine ratio was significantly (P < 0.05) reduced. Pyridinoline/creatinine ratio fell from 66.3 (4) [mean (SEM)] to 46.2 (3) μmol/μmol (P < 0.01) and deoxypyridinoline/creatinine ratio fell from 11.5 (1.5) [mean (SEM)] to 7.7 (0.6) μmol/μmol (P < 0.01). There were no differences between the evolution of the biochemical variables in the two groups. Conclusion: These results suggest that oral conjugated equine estrogens and transdermal estradiol, in the given doses, are equally effective in reducing postmenopausal bone resorption.Keywords
This publication has 31 references indexed in Scilit:
- Preventive effects of transdermal administration of 17|3-estradiol on postmenopausal bone loss: A 2-year prospective studyGynecological Endocrinology, 1989
- Estrogen Binding, Receptor mRNA, and Biologic Response in Osteoblast-Like Osteosarcoma CellsScience, 1988
- Dose dependent response of symptoms, pituitary, and bone to transdermal oestrogen in postmenopausal women.BMJ, 1986
- Biologic Effects of Transdermal EstradiolNew England Journal of Medicine, 1986
- The Effect of Estrogen Dose on Postmenopausal Bone LossNew England Journal of Medicine, 1983
- PREVENTION OF SPINAL OSTEOPOROSIS IN OOPHORECTOMISED WOMENThe Lancet, 1980
- SERUM EQUILIN, ŒSTRONE, AND ŒSTRADIOL LEVELS IN POSTMENOPAUSAL WOMEN RECEIVING CONJUGATED EQUINE ŒSTROGENS ('PREMARIN')The Lancet, 1980
- Randomization Analysis of the Completely Randomized Design Extended to Growth and Response CurvesJournal of the American Statistical Association, 1979
- DIAGNOSTIC PROCEDURES IN DISORDERS OF CALCIUM METABOLISMClinical Endocrinology, 1978
- EFFECTS OF NATURAL AND ARTIFICIAL MENOPAUSE ON PLASMA AND URINARY CALCIUM AND PHOSPHORUSThe Lancet, 1967