Moderation of the daily dose of HRT: prevention of osteoporosis

被引:0
作者
Gallagher, JC [1 ]
机构
[1] Creighton Univ, Sch Med, Omaha, NE 68178 USA
关键词
osteoporosis; low-dose; HRT; tolerability; compliance;
D O I
暂无
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Introduction and methods: Osteoporosis is the most common bone disease in clinical practice. Between 30% and 50% of postmenopausal women and almost 50% of all people over the age of 75 are estimated to have osteoporosis. HRT is well known for reducing the risk of osteoporosis in postmenopausal women but compliance with long-term HRT therapy remains low. The use of low dose HRT reduces the estrogenic adverse events which often cause patients to stop therapy. In this paper, the current literature on the benefits of low dose HRT and osteoporosis prevention are reviewed. Results: Various studies have assessed the efficacy of low-dose HRT (25 mcg/day transdermally; 0.3 mg/day orally) in the prevention of osteoporosis. Low dose HRT is effective at reducing bone loss in postmenopausal and oophorectomised women. In one study of 218 postmenopausal women, a dose of 0.3 mg/day of esterified estrogen resulted in a small but significant increase in whole body BMD compared to a decrease in the placebo group. The addition of calcium supplements may have a synergistic effect on the reduction of bone loss. Conclusion: Low dose estrogen, taken either orally or transdermally, can prevent or reverse postmenopausal bone loss and appears to be a useful alternative to higher dosages in the prevention and treatment of osteoporosis. The option of starting HRT at low dose gives physicians the ability to titrate doses to suit individual patients whilst ensuring adequate bone protection and the minimum of hyperestrogenic side effects. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:S57 / S63
页数:7
相关论文
共 28 条
[21]   Prevention of postmenopausal bone loss with minimal uterine bleeding using low dose continuous estrogen/progestin therapy: A 2-year prospective study [J].
Mizunuma, H ;
Okano, H ;
Soda, M ;
Kagami, I ;
Miyamoto, S ;
Tokizawa, T ;
Honjo, S ;
Ibuki, Y .
MATURITAS, 1997, 27 (01) :69-76
[22]   ESTROGEN DEFICIENCY AND RISK OF ALZHEIMERS-DISEASE IN WOMEN [J].
PAGANINIHILL, A ;
HENDERSON, VW .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1994, 140 (03) :256-261
[23]   PHARMACOKINETICS AND PHARMACODYNAMICS OF TRANSDERMAL DOSAGE FORMS OF 17-BETA-ESTRADIOL - COMPARISON WITH CONVENTIONAL ORAL ESTROGENS USED FOR HORMONE REPLACEMENT [J].
POWERS, MS ;
SCHENKEL, L ;
DARLEY, PE ;
GOOD, WR ;
BALESTRA, JC ;
PLACE, VA .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1985, 152 (08) :1099-1106
[24]   THE MENOPAUSE REVISITED [J].
SAMSIOE, G .
INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 1995, 51 (01) :1-13
[25]   Timing of postmenopausal estrogen for optimal bone mineral density - The Rancho Bernardo study [J].
Schneider, DL ;
BarrettConnor, EL ;
Morton, DJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 277 (07) :543-547
[26]   DIETARY-INTAKE OF CALCIUM AND POSTMENOPAUSAL BONE LOSS [J].
STEVENSON, JC ;
WHITEHEAD, MI ;
PADWICK, M ;
ENDACOTT, JA ;
SUTTON, C ;
BANKS, LM ;
FREEMANTLE, C ;
SPINKS, TJ ;
HESP, R .
BRITISH MEDICAL JOURNAL, 1988, 297 (6640) :15-17
[27]   EFFECTS OF TRANSDERMAL VERSUS ORAL HORMONE REPLACEMENT THERAPY ON BONE-DENSITY IN SPINE AND PROXIMAL FEMUR IN POSTMENOPAUSAL WOMEN [J].
STEVENSON, JC ;
CUST, MP ;
GANGAR, KF ;
HILLARD, TC ;
LEES, B ;
WHITEHEAD, MI .
LANCET, 1990, 336 (8710) :265-269