Oregon Osteoporosis Center, 5050 NE Hoyt, Suite 626, Portland, OR 97213, USA.
Osteoporos Int. 2013 Jan;24(1):293-9. doi: 10.1007/s00198-012-2056-0. Epub 2012 Jun 30.
This study showed that risedronate 150-mg once a month provides similar efficacy and safety at 2 years compared with risedronate 5-mg daily for the treatment of postmenopausal osteoporosis. This adds to the range of risedronate dosing options and provides an alternative for patients who prefer once-a-month dosing.
Risedronate is effective in the treatment of postmenopausal osteoporosis in oral daily, weekly, or on two consecutive days per month doses. This 2-year randomized, double-blind, multicenter study assesses the efficacy and safety of a single risedronate 150-mg once-a-month oral dose compared with the 5-mg daily regimen.
Women with postmenopausal osteoporosis were randomly assigned to receive risedronate 5-mg daily (n = 642) or 150-mg once a month (n = 650) for 2 years. Bone mineral density (BMD), bone turnover markers, new vertebral fractures, and adverse events were evaluated. The primary efficacy endpoint was the mean percent change from baseline in lumbar spine BMD after 1 year.
Four hundred ninety-eight subjects in the daily group (77.6 %) and 513 subjects in the once-a-month group (78.9 %) completed the study. After 24 months, the mean percent change in lumbar spine BMD was 3.9 % (95 % confidence interval [CI], 3.43 to 4.42 %) and 4.2 % (95 % CI, 3.68 to 4.65 %) in the daily and once-a-month groups, respectively. The once-a-month regimen was determined to be non-inferior to the daily regimen. The mean percent changes in BMD at the hip were similar in both dose groups, as were changes in biochemical markers of bone turnover. The incidence of adverse events, adverse events leading to withdrawal, and upper gastrointestinal tract adverse events were similar in the two treatment groups.
After 2 years, treatment with risedronate 150-mg once a month provided similar efficacy and tolerability to daily dosing and provides an alternative for patients who prefer once-a-month oral dosing.
本研究表明,与每日服用利塞膦酸钠 5mg 相比,每月服用利塞膦酸钠 150mg 一次同样具有 2 年的疗效和安全性,为利塞膦酸钠的给药方案提供了更多选择,并为喜欢每月一次口服剂量的患者提供了另一种选择。
利塞膦酸钠在口服每日、每周或每月连续两天的剂量治疗绝经后骨质疏松症中是有效的。这项为期 2 年的随机、双盲、多中心研究评估了单次口服利塞膦酸钠 150mg 每月一次与每日 5mg 方案相比的疗效和安全性。
绝经后骨质疏松症女性随机分为每日服用利塞膦酸钠 5mg(n=642)或每月一次服用利塞膦酸钠 150mg(n=650),共 2 年。评估骨密度(BMD)、骨转换标志物、新椎体骨折和不良事件。主要疗效终点是 1 年后腰椎 BMD 从基线的平均百分比变化。
每日组有 498 名(77.6%)和每月组有 513 名(78.9%)受试者完成了研究。24 个月后,腰椎 BMD 的平均百分比变化分别为每日组 3.9%(95%置信区间[CI],3.43 至 4.42%)和每月组 4.2%(95%CI,3.68 至 4.65%)。每月方案被确定为不劣于每日方案。两组的髋部 BMD 平均变化相似,骨转换生化标志物的变化也相似。两组的不良事件发生率、导致停药的不良事件和上消化道不良事件相似。
2 年后,每月服用利塞膦酸钠 150mg 的疗效和耐受性与每日服用相同,为喜欢每月一次口服剂量的患者提供了另一种选择。