Resistance of pelvic arteries and plasma lipids in postmenopausal women: Comparative study of tibolone and continuous combined estradiol and norethindrone acetate replacement therapy

Citation
M. Doren et al., Resistance of pelvic arteries and plasma lipids in postmenopausal women: Comparative study of tibolone and continuous combined estradiol and norethindrone acetate replacement therapy, AM J OBST G, 183(3), 2000, pp. 575-582
Citations number
25
Categorie Soggetti
Reproductive Medicine","da verificare
Journal title
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
ISSN journal
00029378 → ACNP
Volume
183
Issue
3
Year of publication
2000
Pages
575 - 582
Database
ISI
SICI code
0002-9378(200009)183:3<575:ROPAAP>2.0.ZU;2-X
Abstract
OBJECTIVE: We sought to compare vascular resistance and plasma lipids in po stmenopausal women assigned to tibolone (a synthetic estrogen replacement s teroid) therapy or continuous combined hormone replacement therapy. STUDY DESIGN: Pulsatility and resistance indexes in pelvic arteries (color Doppler transvaginal ultrasonography) and lipids were monitored in this dou ble-blind 1-year trial of 100 women randomized to either 2.5 mg tibolone or 2 mg 17 beta-estradiol plus 1 mg norethindrone acetate daily. RESULTS: Both indexes of the arcuate arteries (uterine arteries) were signi ficantly reduced beyond 3 and 6 months (12 months) from baseline, respectiv ely, by the combined regimen compared with tibolone alone. Tibolone increas ed the resistance index of arcuate arteries but did not affect uterine arte ries. There was no effect of either regimen on the internal iliac arteries. The medians of the percentage changes from baseline of high-density lipopr otein cholesterol (triglycerides) were significant between groups after 1 y ear, as follows: -17% (-16%) in the tibolone group and -4% (+15%) in the co mbined group, respectively. Both regimens similarly reduced total and low-d ensity lipoprotein cholesterol and lipoprotein Lp(a). CONCLUSION: Hormone replacement therapy may induce different or opposite ch anges of both vascular resistance and lipids. It is unknown whether these f indings may modify cardiovascular risk.