HORMONE REPLACEMENT THERAPY WITH DYDROGESTERONE AND 17-BETA-ESTRADIOL- EFFECTS ON SERUM-LIPOPROTEINS AND GLUCOSE-TOLERANCE DURING 24 MONTHFOLLOW-UP

Citation
D. Crook et al., HORMONE REPLACEMENT THERAPY WITH DYDROGESTERONE AND 17-BETA-ESTRADIOL- EFFECTS ON SERUM-LIPOPROTEINS AND GLUCOSE-TOLERANCE DURING 24 MONTHFOLLOW-UP, British journal of obstetrics and gynaecology, 104(3), 1997, pp. 298-304
Citations number
26
Categorie Soggetti
Obsetric & Gynecology
ISSN journal
03065456
Volume
104
Issue
3
Year of publication
1997
Pages
298 - 304
Database
ISI
SICI code
0306-5456(1997)104:3<298:HRTWDA>2.0.ZU;2-V
Abstract
Objective To assess serum lipid and lipoprotein concentrations and ora l glucose tolerance in postmenopausal women treated with 17 beta-oestr adiol (2 mg/day) and cyclical dydrogesterone (10 mg/day for 14 days pe r 28 day cycle). Design A 24 month prospective study of 29 women actin g as their own controls. On-treatment samples were taken during the co mbined (oestrogen-progestogen) phase of therapy. Setting Metabolic res earch unit in London. Population Postmenopausal women with no previous exposure to hormone replacement therapy attending a menopause clinic in a London hospital. Methods Fasting serum sampling and oral glucose tolerance testing. Main outcome measures Serum lipids and lipoprotein concentrations and plasma glucose, insulin and C-peptide responses to an oral glucose load. Results Restricting the analysis to the 17 women who completed the study, no effect was seen on serum triglyceride con centrations. There was a mean fall of 5.9% (95% CI 1.2 to -13.0) in co ncentrations of serum total cholesterol, reflecting the balance of a 1 0.7% fall (95% CI 4.3 to -25.8) in low density lipoprotein cholesterol concentrations and a 16.3% increase (95% CI 7.3 to -25.3) in those of high density lipoproteins. Fasting glucose concentrations and glucose tolerance test responses were unchanged. Fasting insulin concentratio ns fell substantially (-41.6%, 95% CI -23.4 to -59.8) with falls also being seen in insulin responses to glucose. Fasting C-peptide concentr ations increased by 36.2% (95% CI 9.17 to 63.3), with no consistent ef fect on C-peptide responses to glucose. Conclusions Dydrogesterone did not appear to oppose the potentially beneficial effects of oestradiol on insulin or either low or high density lipoproteins, making the com bination with 17 beta-oestradiol a potentially useful option for postm enopausal women particularly those at risk of cardiovascular disease o r diabetes mellitus.