MRC Lifecourse Epidemiology Unit, University of Southampton and NIHR Musculoskeletal Biomedical Research Unit, University of Oxford, UK.
Curr Med Res Opin. 2012 Feb;28(2):231-9. doi: 10.1185/03007995.2011.648758. Epub 2012 Jan 17.
The osteoporosis drug strontium ranelate dissociates bone remodelling processes. It also inhibits subchondral bone resorption and stimulates cartilage matrix formation in vitro. Exploratory studies in the osteoporosis trials report that strontium ranelate reduces biomarkers of cartilage degradation, and attenuates the progression and clinical symptoms of spinal osteoarthritis, suggesting symptom- and structure-modifying activity in osteoarthritis. We describe the rationale and design of a randomised trial evaluating the efficacy and safety of strontium ranelate in knee osteoarthritis.
RESEARCH DESIGN, METHODS, AND RESULTS: This double-blind, placebo-controlled trial (98 centres, 18 countries) includes ambulatory Caucasian men and women aged ≥50 years with primary knee osteoarthritis of the medial tibiofemoral compartment (Kellgren and Lawrence grade 2 or 3), joint space width (JSW) 2.5 to 5 mm, and knee pain on most days in the previous month (intensity ≥40 mm on a visual analogue scale). Patients are randomly allocated to three groups (strontium ranelate 1 or 2 g/day, or placebo). Follow-up is expected to last 3 years. The primary endpoint is radiographic change in JSW from baseline in each group versus placebo. The main clinical secondary endpoint is WOMAC score at the knee. Safety is assessed at every visit. It is estimated that 1600 patients are required to establish statistical significance with power >90% (0.2 mm ± 10% between-group difference in change in JSW over 3 years). Recruitment started in April 2006. The results are expected in spring 2012.
The trial is registered on www.controlled-trials.com (number ISRCTN41323372).
This randomised, double blind, placebo-controlled study will establish the potential of strontium ranelate in improving structure and symptoms in patients with knee osteoarthritis.
骨质疏松药物雷奈酸锶可使骨重建过程解体。它还可抑制软骨下骨吸收并刺激体外软骨基质形成。在骨质疏松试验中的探索性研究报告称,雷奈酸锶可降低软骨降解生物标志物的水平,并可减轻脊柱骨关节炎的进展和临床症状,表明其在骨关节炎中具有改善症状和结构的作用。我们描述了一项随机试验的原理和设计,该试验旨在评估雷奈酸锶治疗膝骨关节炎的疗效和安全性。
研究设计、方法和结果:这是一项双盲、安慰剂对照试验(98 个中心,18 个国家),纳入了年龄≥50 岁的、有症状的、活动期的、膝内侧胫股关节(Kellgren 和 Lawrence 分级 2 或 3 级)的、关节间隙宽度(JSW)为 2.5 至 5mm 的、且在过去 1 个月内多数日子有膝关节疼痛(视觉模拟评分≥40mm)的白人男性和女性原发性膝骨关节炎患者。患者被随机分配到 3 个治疗组(雷奈酸锶 1 或 2g/天或安慰剂)。预计随访 3 年。主要的影像学终点是 JSW 与基线相比的变化,次要的临床终点是膝关节 WOMAC 评分。安全性在每次就诊时评估。预计需要 1600 例患者才能以 90%以上的效能(3 年时 JSW 变化的组间差异为 0.2mm ± 10%)来确立统计学意义。招募工作于 2006 年 4 月开始。结果预计于 2012 年春季公布。
该试验在 www.controlled-trials.com(注册号 ISRCTN41323372)上注册。
这项随机、双盲、安慰剂对照研究将确定雷奈酸锶在改善膝骨关节炎患者结构和症状方面的潜力。