Comparative metabolic study of percutaneous versus oral micronized 17β-oestradiol in replacement therapy

• Published in: Maturitas Vol. 11; no. 4; pp. 275 - 286
• Main Authors: de Moustier, B.Faguer, Conard, J., Guyene, T.T., Sitt, Y., Denys, I., Arnoux-Rouveyre, M., Pelissier, C.
• Format: Journal Article
• Language: English
• Published: Shannon Elsevier Ireland Ltd 01.12.1989; Elsevier Science
• Subjects: Administration, Cutaneous; Administration, Oral; Angiotensinogen - blood; Angiotensinogen - drug effects; Biological and medical sciences; Blood pressure; Body Weight - drug effects; Bones, joints and connective tissue. Antiinflammatory agents; Coagulation; Estradiol - administration & dosage; Estradiol - blood; Estradiol - therapeutic use; Estrogen Replacement Therapy; Female; Hormone replacement therapy; Humans; Lipoproteins; Lipoproteins - blood; Medical sciences; Osteoporosis, Postmenopausal - prevention & control; Pharmacology. Drug treatments; Post-menopause; Prospective Studies; Randomized Controlled Trials as Topic; Renin substrate; Sex Hormone-Binding Globulin - metabolism; Lipoproteins; Hormone replacement therapy; Blood pressure; Renin substrate; Coagulation; Post-menopause; Therapeutic efficiency; Human; Steroid; Menopause; Diseases of the osteoarticular system; Oral administration; Metabolism; Route of administration; Estradiol; Percutaneous route; Osteoporosis; Chemotherapy; Anabolic agent; Comparative study
• ISSN: 0378-5122; 1873-4111
• DOI: 10.1016/0378-5122(89)90024-8

The aim of this study was to compare the metabolic effects of two presentations of 17β-oestradiol (E 2) which are of recognized effectiveness in the prevention of post-menopausal bone loss, one being administered via the oral and the other via the percutaneous route. During this prospective, randomized study, 32 patients were treated for 2 mth with either 2 mg/day of oral micronized E 2 ( n = 16) or 3–5 mg/day of percutaneous E 2 ( n = 16). Both regimens proved efficacious, since significant increases in oestrone (E 1) and E 2 concentrations ranging up to mid-follicular values were observed. In the percutaneous-treatment group we noted a significant decrease in triglycerides (TG), without any significant changes in high-density lipoprotein cholesterol (HDL-C) or low-density lipoprotein cholesterol (LDL-C). In the oral-treatment group, we saw no significant increase in HDL-C, although significant increases were observed in body weight, TG, plasma renin substrate (PRS) and sexhormone-binding globulin (SHBG) as well as significant decreases in antithrombin III (AT III) activity and antigen. All of these metabolic variations led us to the conclusion that oral E 2 at the dose established as effective in preventing post-menopausal osteoporosis may, even when micronized, alter certain metabolic and haemostatic parameters in a population characterized by increases in cardiovascular risk factors and morbidity. Oral oestrogen replacement therapy should therefore continue to be used only in carefully selected patients and be strictly followed up by systematic checks on a series of metabolic criteria.