Efficacy and safety of raloxifene 60 milligrams/day in postmenopausal Asian women

被引:35
作者
Kung, AWC
Chao, HT
Huang, KE
Need, AG
Taechakraichana, N
Loh, FH
Gonzaga, F
Sriram, U
Ismail, NMN
Farooqi, A
Rachman, IA
Crans, GG
Wong, M
Thiebaud, D [1 ]
机构
[1] Univ Hong Kong, Dept Med, Div Endocrinol, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
[2] Vet Gen Hosp, Dept Obstet & Gynecol, Taipei 112, Taiwan
[3] Chang Gung Mem Hosp, Dept Obstet & Gynecol, Kaohsiung 833, Taiwan
[4] Inst Med & Vet Sci, Adelaide, SA 5000, Australia
[5] Chulalongkorn Univ Hosp, Dept Obstet & Gynecol, Bangkok 10330, Thailand
[6] Natl Univ Singapore Hosp, Dept Obstet & Gynecol, Singapore 119074, Singapore
[7] Univ Philippines, Dept Obstet & Gynecol, Philippine Gen Hosp, Manila 1000, Philippines
[8] EV Kalyani Med Ctr, Madras 600004, Tamil Nadu, India
[9] Hosp Univ Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia
[10] Pakistan Inst Med Sci, Dept Rheumatol & Phys Med, Islamabad, Pakistan
[11] Univ Indonesia, Dept Obstet & Gynecol, Dr Cipto Mangunkusumo Hosp Sch Med, Jakarta 10430, Indonesia
[12] Eli Lilly & Co, Lilly Res Labs, Indianapolis, IN 46285 USA
[13] Eli Lilly Australia Pty Ltd, W Ryde, NSW 2114, Australia
关键词
D O I
10.1210/jc.2002-021855
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
In healthy Caucasian postmenopausal women, raloxifene increases bone mineral density (BMD), decreases biochemical markers of bone turnover, and lowers low-density lipoprotein (LDL) cholesterol, without effects on high-density lipoprotein (HDL) cholesterol and triglycerides. This randomized, double-blind study examines the effects of raloxifene 60 mg/d (n = 483) or placebo (n = 485) in healthy postmenopausal Asian women ( mean age 57 yr) from Australia, Hong Kong, India, Indonesia, Malaysia, Pakistan, Philippines, Singapore, Taiwan, and Thailand. Serum osteocalcin, serum N-telopeptide, total cholesterol, HDL cholesterol, LDL cholesterol, and triglycerides were assessed at baseline and 6 months. Lumbar spine BMD was measured at baseline and 1 yr in 309 women from 4 countries. Clinical adverse events were recorded at each interim visit. At 6 months, raloxifene 60 mg/d significantly decreased osteocalcin, N-telopeptide, total cholesterol, and LDL cholesterol by medians of 15.9%, 14.6%, 5.3%, and 7.7%, respectively, from placebo. Changes in HDL cholesterol and triglycerides were similar between raloxifene and placebo. Raloxifene 60 mg/d increased mean lumbar spine BMD (1.9%) from placebo at 1 yr ( P = 0.0003). The incidences of hot flashes ( placebo 3.5%, raloxifene 5.6%, P = 0.12), and leg cramps ( placebo 2.7%, raloxifene 4.3%, P = 0.16) were not different between groups. No case of venous thromboembolism was reported. The effects of raloxifene 60 mg/d on bone turnover, BMD, and serum lipids in healthy postmenopausal Asian women were similar to that previously reported in Caucasian women.
引用
收藏
页码:3130 / 3136
页数:7
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