Differential impact of conventional oral or transdermal hormone replacement therapy or tibolone on body composition in postmenopausal women

被引:58
|
作者
Hänggi, W
Lippuner, K
Jaeger, P
Birkhäuser, MH
Horber, FF
机构
[1] Univ Bern, Div Endocrinol, Dept Gynaecol & Obstet, Bern, Switzerland
[2] Univ Hosp Bern, Policlin Med, CH-3010 Bern, Switzerland
[3] Klin Hirslanden, Dept Internal Med, Zurich, Switzerland
关键词
D O I
10.1046/j.1365-2265.1998.00481.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To compare the effects on body composition and body weight of tibolone vs two different sequential oral or transdermal oestrogen-progestogen hormone replacement therapies versus no therapy. PATIENTS AND METHODS One hundred postmenopausal women were assigned to a control group (n=26), or randomized to 1) tibolone (TIB) 2.5 mg/day (n=28), 2) oral oestradiol 2 mg/day (PO) plus sequential dydrogesterone 10 mg/day for 14 of 28 days per cycle (n=26), or 3) transdermal oestradiol patch (TTS) releasing 50 mu g/day plus oral sequential dydrogesterone 10 mg/day for 14 of 28 days per cycle (n = 20). Body composition was measured at the baseline and every 6 months for 2 years by DXA (Hologic QDR 1000 W). RESULTS Total body fat mass increased (P<0.05) in controls (+3.6+/-1.5%) and in TTS treated (+4.7 +/- 2.2%), but not in PO (-1.2 +/- 2.4%) and TIB (-1.6 +/- 2 2%) treated subjects. This increase in total fat mass in controls and TTS treated women was mostly due to an increase in fat mass of the trunk (P< 0.05), but not legs. As a result, a redistribution of body fat to the trunk occurred in controls, TTS and TIB, but not in PO treated women (P<0.05). Total lean body mass decreased (P< 0.02) in controls (-1.7 +/- 0.7%) and PO (-1.4 +/- 0.6%), but not in TTS (+ 0.3 +/- 0.8%) and TIB (+ 0 4 +/- 0 5%) treated subjects. CONCLUSIONS The menopause is associated with an increase in total body fat and a decline in lean body mass. Oral oestradiol/dydrogesterone and tibolone prevent total body fat changes, whereas transdermal oestradiol/oral dydrogesterone and tibolone prevent the lean mass changes. Furthermore, oral oestradiol/dydrogesterone prevents the shift to a central, android fat distribution.
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页码:691 / 699
页数:9
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