Cole Raymond E, Harris Steven T
Department of Internal Medicine, Michigan State University College of Osteopathic Medicine, Michigan, USA.
Medscape J Med. 2009;11(1):12. Epub 2009 Jan 13.
Nonvertebral fractures (NVFs) are the most costly and disabling type of osteoporotic fractures. Bisphosphonate therapy effectively reduces the risk for NVFs; however, fracture protection depends critically on adherence and persistence. Approved bisphosphonate regimens with extended dosing intervals increase patient convenience, help patients remain on therapy, and improve fracture protection in clinical practice.
To assess evidence for NVF reduction with extended-interval bisphosphonates, we searched PubMed for phase 3 clinical trials, meta-analyses, and reviews of approved nitrogen-containing bisphosphonate regimens with monthly or less frequent dosing (monthly oral ibandronate, monthly or intermittent oral risedronate, quarterly intravenous [IV] ibandronate, and yearly IV zoledronic acid). These references were augmented by ISI Web of Science cited reference searches, ISI Proceedings searches, and hand searches of relevant conference proceedings and review bibliographies.
Monthly oral and quarterly IV ibandronate reduce NVF risk significantly more than daily oral ibandronate and placebo, as shown by meta-analyses stratified by ibandronate dose (annual cumulative exposure). Intermittent and monthly oral risedronate have shown bone density gains similar to those seen with daily oral risedronate. Incidence rates of NVF, reported as adverse events, were also similar. Yearly IV zoledronic acid reduced NVF risk by 25% and hip fracture risk by 41% compared with placebo in its pivotal trial for postmenopausal osteoporosis.
Extended-interval bisphosphonates offer similar or superior NVF protection with less lifestyle disruption compared with daily or weekly treatment. By removing obstacles to adherence and persistence, extended-interval oral and IV bisphosphonate regimens provide valuable therapeutic options to enhance real-world effectiveness and reduce NVF incidence.
非椎体骨折(NVF)是骨质疏松性骨折中代价最高且导致残疾的类型。双膦酸盐疗法可有效降低非椎体骨折的风险;然而,骨折预防在很大程度上取决于依从性和持续性。批准的延长给药间隔的双膦酸盐方案增加了患者的便利性,有助于患者持续接受治疗,并在临床实践中提高骨折预防效果。
为评估延长间隔双膦酸盐降低非椎体骨折的证据,我们在PubMed上搜索了3期临床试验、荟萃分析以及关于批准的每月或更不频繁给药的含氮双膦酸盐方案(每月口服伊班膦酸钠、每月或间歇口服利塞膦酸钠、每季度静脉注射[IV]伊班膦酸钠和每年静脉注射唑来膦酸)的综述。通过ISI科学网引用参考文献搜索、ISI会议录搜索以及对相关会议录和综述参考文献的手工搜索对这些参考文献进行了补充。
荟萃分析按伊班膦酸钠剂量(年度累积暴露量)分层显示,每月口服和每季度静脉注射伊班膦酸钠比每日口服伊班膦酸钠和安慰剂更能显著降低非椎体骨折风险。间歇和每月口服利塞膦酸钠的骨密度增加与每日口服利塞膦酸钠相似。作为不良事件报告的非椎体骨折发生率也相似。在绝经后骨质疏松症的关键试验中,与安慰剂相比,每年静脉注射唑来膦酸使非椎体骨折风险降低25%,髋部骨折风险降低41%。
与每日或每周治疗相比,延长间隔双膦酸盐在减少生活方式干扰的情况下提供相似或更好的非椎体骨折保护。通过消除依从性和持续性的障碍,延长间隔口服和静脉注射双膦酸盐方案提供了有价值的治疗选择,以提高实际疗效并降低非椎体骨折发生率。