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雷奈酸锶治疗绝经后骨质疏松症 10 年以上的抗骨折疗效维持。

Maintenance of antifracture efficacy over 10 years with strontium ranelate in postmenopausal osteoporosis.

机构信息

Department of Public Health and Health Economics, University of Liège, Liège, Belgium.

出版信息

Osteoporos Int. 2012 Mar;23(3):1115-22. doi: 10.1007/s00198-011-1847-z. Epub 2011 Nov 29.

Abstract

UNLABELLED

In an open-label extension study, BMD increased continuously with strontium ranelate over 10 years in osteoporotic women (P < 0.01). Vertebral and nonvertebral fracture incidence was lower between 5 and 10 years than in a matched placebo group over 5 years (P < 0.05). Strontium ranelate's antifracture efficacy appears to be maintained long term.

INTRODUCTION

Strontium ranelate has proven efficacy against vertebral and nonvertebral fractures, including hip, over 5 years in postmenopausal osteoporosis. We explored long-term efficacy and safety of strontium ranelate over 10 years.

METHODS

Postmenopausal osteoporotic women participating in the double-blind, placebo-controlled phase 3 studies SOTI and TROPOS to 5 years were invited to enter a 5-year open-label extension, during which they received strontium ranelate 2 g/day (n = 237, 10-year population). Bone mineral density (BMD) and fracture incidence were recorded, and FRAX® scores were calculated. The effect of strontium ranelate on fracture incidence was evaluated by comparison with a FRAX®-matched placebo group identified in the TROPOS placebo arm.

RESULTS

The patients in the 10-year population had baseline characteristics comparable to those of the total SOTI/TROPOS population. Over 10 years, lumbar BMD increased continuously and significantly (P < 0.01 versus previous year) with 34.5 ± 20.2% relative change from baseline to 10 years. The incidence of vertebral and nonvertebral fracture with strontium ranelate in the 10-year population in years 6 to 10 was comparable to the incidence between years 0 and 5, but was significantly lower than the incidence observed in the FRAX®-matched placebo group over 5 years (P < 0.05); relative risk reductions for vertebral and nonvertebral fractures were 35% and 38%, respectively. Strontium ranelate was safe and well tolerated over 10 years.

CONCLUSIONS

Long-term treatment with strontium ranelate is associated with sustained increases in BMD over 10 years, with a good safety profile. Our results also support the maintenance of antifracture efficacy over 10 years with strontium ranelate.

摘要

目的

在一项开放标签延伸研究中,雷奈酸锶可使骨质疏松女性的骨密度持续增加,持续时间超过 10 年(P<0.01)。5 至 10 年期间,椎体和非椎体骨折的发生率低于 5 年时匹配安慰剂组(P<0.05)。雷奈酸锶的抗骨折疗效似乎长期保持。

简介

雷奈酸锶对椎体和非椎体骨折(包括髋部骨折)具有 5 年以上的疗效,已在绝经后骨质疏松症中得到证实。我们探索了雷奈酸锶 10 年以上的长期疗效和安全性。

方法

参加双盲、安慰剂对照的 SOTI 和 TROPOS 期 3 研究至 5 年的绝经后骨质疏松女性被邀请进入为期 5 年的开放标签延伸期,在此期间她们接受雷奈酸锶 2g/天(n=237,10 年人群)。记录骨密度(BMD)和骨折发生率,并计算 FRAX®评分。通过与 TROPOS 安慰剂组中根据 FRAX®匹配的安慰剂组进行比较,评估雷奈酸锶对骨折发生率的影响。

结果

10 年人群的患者具有与 SOTI/TROPOS 总人群相似的基线特征。在 10 年期间,腰椎 BMD 持续显著增加(P<0.01,与前一年相比),与基线相比有 34.5±20.2%的相对变化至 10 年。在 10 年人群中,雷奈酸锶在第 6 至 10 年的椎体和非椎体骨折发生率与第 0 至 5 年的发生率相当,但明显低于 FRAX®匹配的安慰剂组在 5 年内的发生率(P<0.05);椎体和非椎体骨折的相对风险降低分别为 35%和 38%。雷奈酸锶在 10 年内安全且耐受性良好。

结论

雷奈酸锶长期治疗可使 BMD 在 10 年内持续增加,安全性良好。我们的结果还支持雷奈酸锶在 10 年内保持抗骨折疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e9c/3277702/ea6603e571b2/198_2011_1847_Fig1_HTML.jpg

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