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雷奈酸锶治疗绝经后骨质疏松症:批判性评价。

Strontium ranelate in postmenopausal osteoporosis treatment: a critical appraisal.

机构信息

Department of Internal Medicine.

出版信息

Int J Womens Health. 2010 Aug 9;2:1-6.

PMID:21072291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2971725/
Abstract

Osteoporosis is a progressive and debilitating disease characterized by a massive bone loss with a deterioration of bone tissues, and a propensity for a fragility fracture. Strontium ranelate is the first antiosteoporotic treatment that has dual mode of action and simultaneously increases bone formation, while decreasing bone resorption, thus rebalancing bone turnover formation. Strontium ranelate rebalances bone turnover in favor of improved bone geometry, cortical thickness, trabecular bone morphology and intrinsic bone tissue quality, which translates into enhanced bone strength. This review describes the mechanism of the strontium ranelate action and its effects on bone mineral density, bone turnover, and osteoporotic fractures. The efficacy of strontium ranelate in postmenopausal osteoporosis treatment to reduce the risk of vertebral and hip fractures has been highlighted in several randomized, controlled trials. Treatment efficacy with strontium ranelate has been documented across a wide range of patient profiles: age, number of prevalent vertebral fractures, body mass index, and a family history of osteoporosis. Because strontium ranelate has a large spectrum of efficacy, it can be used to treat different subgroups of patients with postmenopausal osteoporosis. Strontium ranelate was shown to be relatively well tolerated and the safety aspects were good. Strontium ranelate should be considered as a first-line treatment for postmenopausal osteoporotic patients.

摘要

骨质疏松症是一种进行性和使人虚弱的疾病,其特征是大量骨质流失,骨组织恶化,容易发生脆性骨折。雷奈酸锶是第一种具有双重作用的抗骨质疏松药物,它可以同时增加骨形成,减少骨吸收,从而重新平衡骨转换形成。雷奈酸锶重新平衡骨转换,有利于改善骨几何形状、皮质厚度、小梁骨形态和内在骨组织质量,从而提高骨强度。本文描述了雷奈酸锶的作用机制及其对骨密度、骨转换和骨质疏松性骨折的影响。雷奈酸锶在绝经后骨质疏松症治疗中降低椎体和髋部骨折风险的疗效已在多项随机对照试验中得到证实。雷奈酸锶的治疗效果在广泛的患者人群中得到了证明:年龄、椎体骨折数量、体重指数和骨质疏松家族史。由于雷奈酸锶具有广泛的疗效,它可以用于治疗不同亚组的绝经后骨质疏松症患者。雷奈酸锶显示出相对良好的耐受性,安全性良好。雷奈酸锶应被视为绝经后骨质疏松症患者的一线治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/708f/2971725/1cd0c49b6127/ijwh-2-001f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/708f/2971725/1cd0c49b6127/ijwh-2-001f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/708f/2971725/1cd0c49b6127/ijwh-2-001f1.jpg

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Osteoporos Int. 2008 Dec;19(12):1811-2. doi: 10.1007/s00198-008-0734-8. Epub 2008 Sep 20.
2
Effects of long-term strontium ranelate treatment on the risk of nonvertebral and vertebral fractures in postmenopausal osteoporosis: Results of a five-year, randomized, placebo-controlled trial.长期使用雷奈酸锶治疗对绝经后骨质疏松症患者非椎体和椎体骨折风险的影响:一项为期五年的随机安慰剂对照试验结果
Arthritis Rheum. 2008 Jun;58(6):1687-95. doi: 10.1002/art.23461.
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History of cardiovascular events and cardiovascular risk factors among patients initiating strontium ranelate for treatment of osteoporosis.
开始使用雷奈酸锶治疗骨质疏松症的患者的心血管事件史和心血管危险因素
Int J Womens Health. 2015 Nov 17;7:913-8. doi: 10.2147/IJWH.S88627. eCollection 2015.
4
Strontium ranelate as an adjuvant for fracture healing: clinical, radiological, and ultrasound findings in a randomized controlled study on wrist fractures.雷奈酸锶作为骨折愈合的辅助药物:手腕骨折随机对照研究的临床、放射学及超声检查结果
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Enhancement of orthodontic anchorage and retention by the local injection of strontium: An experimental study in rats.通过局部注射锶增强正畸支抗和固位:大鼠实验研究
Saudi Dent J. 2015 Jan;27(1):22-9. doi: 10.1016/j.sdentj.2014.08.001. Epub 2014 Oct 24.
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Pharmacological management of osteogenesis.成骨的药理学管理。
Clinics (Sao Paulo). 2014 Jun;69(6):438-46. doi: 10.6061/clinics/2014(06)12.
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Combination of Micronutrients for Bone (COMB) Study: bone density after micronutrient intervention.联合微量营养素对骨骼的研究(COMB 研究):微量营养素干预后的骨密度。
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Evidence based medicine and effective interventions of pharmacological therapy for the prevention of osteoporotic fractures.基于证据的医学及预防骨质疏松性骨折的药物治疗有效干预措施。
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Strontium ranelate prevents quality of life impairment in post-menopausal women with established vertebral osteoporosis.雷奈酸锶可预防已确诊椎体骨质疏松症的绝经后女性生活质量受损。
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J Bone Miner Res. 2007 Sep;22(9):1419-25. doi: 10.1359/jbmr.070607.