Prevention of bone loss in postmenopausal women treated with lasofoxifene compared with raloxifene

被引:103
作者
McClung, Michael R.
Siris, Ethel
Cummings, Steve
Bolognese, Michael
Ettinger, Mark
Moffett, Alfred
Emkey, Ronald
Day, Wesley
Somayaji, Veena
Lee, Andrew
机构
[1] Oregon Osteoporosis Ctr, Portland, OR 97213 USA
[2] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[3] Univ Calif San Francisco, CPMC Res Inst, San Francisco Coordinating Ctr, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[5] Bethesda Hlth Res Ctr, Bethesda, MD USA
[6] Radiant Res, Stuart, FL USA
[7] Radiant Res, Wyomissing, PA USA
[8] Radiant Res, Reading, PA USA
[9] Pfizer Global Res & Dev, La Jolla, CA USA
[10] Pfizer Global Res & Dev, New London, CT USA
来源
MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY | 2006年 / 13卷 / 03期
关键词
lasofoxifene; osteoporosis; bone mineral density; postmenopausal women; LDL cholesterol;
D O I
10.1097/01.gme.0000188736.69617.4f
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Osteoporosis is a significant health problem in postmenopausal women. Consequently, new and effective therapies are being sought to preserve bone mass and prevent osteoporosis in this population of women. The objective of this study was to compare the effects of lasofoxifene with raloxifene and placebo on indices of bone health in postmenopausal women. Design: A randomized, double-blind, placebo- and active treatment-controlled study of 2 years duration was conducted. Women included 410 postmenopausal women aged 47 to 74 years. The four treatment groups were: lasofoxifene 0.25 mg/day or 1.0 mg/day, raloxifene 60 mg/day, or placebo daily. All women received daily calcium and vitamin D supplements. The primary endpoint was percent change from baseline to 2 years in lumbar spine bone mineral density (BMD) in all women having baseline and at least one follow-up bone density measurement. Total hip BMD, biochemical markers of bone turnover, low-density lipoprotein cholesterol, and safety were also evaluated in all women. Results: Both doses of lasofoxifene significantly increased lumbar spine BMD compared with raloxifene (P<0.05) and with placebo treatment (P<0.05). Least squares mean increases (95% CI) from baseline in lumbar spine BMD, compared with placebo, were 3.6% (1.9, 5.2) for lasofoxifene 0.25 mg/day, 3.9% (2.4, 5.5) for lasofoxifene 1.0 mg/day, and 1.7% (0.3, 3.0) for raloxifene. The two doses of lasofoxifene and raloxifene were equally effective at increasing total hip BMD. Lasofoxifene and raloxifene significantly reduced the levels of biochemical markers of bone turnover compared with placebo. In general, the effects of lasofoxifene were greater than the responses to raloxifene. At 2 years, lasofoxifene significantly (P<0.05) reduced low-density lipoprotein cholesterol levels by 20.6% and 19.7% with 0.25 mg/day and I mg/day, respectively, compared with raloxifene (12.1%) and placebo (3.2%). Lasofoxifene and raloxifene had a similar adverse event profile with low rate of discontinuations due to adverse events. Conclusions: Lasofoxifene may be an effective and well-tolerated treatment option for the prevention of bone loss in postmenopausal women.
引用
收藏
页码:377 / 386
页数:10
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