Literature DB >> 15265377

Effects of raloxifene hydrochloride on bone mineral density, bone metabolism and serum lipids in Chinese postmenopausal women with osteoporosis: a multi-center, randomized, placebo-controlled clinical trial.

Jian-li Liu1, Han-min Zhu, Qi-ren Huang, Zhong-lan Zhang, Hui-lin Li, Yue-juan Qin, Ying Zhang, Dao-lin Wei, Jing-hui Lu, Hui Liu, Xiao-ping Chen, Yu-juan Liu, Abie Ekangaki, Yi-man Zheng, Adolfo Diez-Perez, Kristine Harper.   

Abstract

BACKGROUND: Raloxifene has been approved for prevention and treatment of postmenopausal osteoporosis in Caucasian women. It also has some positive effects on serum lipids in Caucasians. The objective of this study was to determine the effect of raloxifene hydrochloride on lumbar spine and total hip bone mineral density (BMD), bone metabolism, and serum lipids in Chinese postmenopausal women with osteoporosis.
METHODS: This was a multi-center, randomized, double-blind, placebo-controlled clinical trial in which 204 postmenopausal Chinese women with osteoporosis were assigned to receive raloxifene (60 mg) or placebo treatment daily for 12 months. BMD, serum bone metabolism markers, and serum lipids were measured before and after drug administration. BMD was measured by Dual-Energy X-Ray Absorptiometry (DEXA) and bone metabolism markers were analyzed by one-step enzyme-linked immunosorbent assay. Serum lipids were measured by enzymatic analysis.
RESULTS: At the end of the 12-month study, lumbar spine BMD increased in both groups with a mean increase of (3.3 +/- 4.8)% in the raloxifene group and (1.0 +/- 4.9)% in the placebo group (P < 0.001). There was a mean increase in total hip BMD of (1.4 +/- 4.8)% in the raloxifene group and a mean decrease of (0.9 +/- 5.0)% in the placebo group (P < 0.001). No subject in the raloxifene group had a new vertebral fracture and 5 placebo subjects had new fractures (P > 0.05). In the raloxifene group, the median decreases in the biochemical markers of bone metabolism serum osteocalcin and C-telopeptide were 41.7% and 61.5%, respectively. These changes were statistically significant compared with those in the placebo group (10.6% and 35.6%, P < 0.001, respectively). Both total cholesterol and low-density lipoprotein cholesterol decreased significantly in the raloxifene group compared with those in the placebo group (P < 0.001, respectively) and there was no significant effect of raloxifene on high-density lipoprotein cholesterol and triglycerides compared with placebo.
CONCLUSIONS: Raloxifene 60 mg/d for 12 months significantly increases lumbar spine and total hip BMD, significantly decreases bone turnover, and has favourable effects on serum lipids in Chinese postmenopausal women with osteoporosis.

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Year:  2004        PMID: 15265377

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN: 0366-6999            Impact factor:   2.628


  3 in total

1.  Effect of raloxifene on clinical fractures in Asian women with postmenopausal osteoporosis.

Authors:  Toshitaka Nakamura; Jian Li Liu; Hirotoshi Morii; Qi Ren Huang; Han Min Zhu; Yongming Qu; Etsuro Hamaya; Daniel Thiebaud
Journal:  J Bone Miner Metab       Date:  2006       Impact factor: 2.626

2.  Denosumab, raloxifene, romosozumab and teriparatide to prevent osteoporotic fragility fractures: a systematic review and economic evaluation.

Authors:  Sarah Davis; Emma Simpson; Jean Hamilton; Marrissa Martyn-St James; Andrew Rawdin; Ruth Wong; Edward Goka; Neil Gittoes; Peter Selby
Journal:  Health Technol Assess       Date:  2020-06       Impact factor: 4.014

3.  Safety and effectiveness profile of raloxifene in long-term, prospective, postmarketing surveillance.

Authors:  Noriko Iikuni; Etsuro Hamaya; Shigeru Nihojima; Shunji Yokoyama; Wakana Goto; Masanori Taketsuna; Akimitsu Miyauchi; Hideaki Sowa
Journal:  J Bone Miner Metab       Date:  2012-07-03       Impact factor: 2.626

  3 in total

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