Cranney Ann, Papaioannou Alexandra, Zytaruk Nicole, Hanley David, Adachi Jonathan, Goltzman David, Murray Timothy, Hodsman Anthony
Department of Medicine, University of Ottawa, Ottawa, Ont.
CMAJ. 2006 Jul 4;175(1):52-9. doi: 10.1503/cmaj.050929.
Human parathyroid hormone (hPTH)(1-34) was approved in 2004 for the treatment of severe osteoporosis. Members of the Osteoporosis Canada clinical guidelines committee conducted a systematic review of randomized controlled trials (RCTs) to assess the efficacy and safety of hPTH for fracture prevention in postmenopausal women and men with osteoporosis.
We searched MEDLINE, EMBASE, HTA, Current Contents and the Cochrane Controlled Trials Registry for published data from 1966 to February 2005. A systematic literature search for RCTs was conducted using the Cochrane Collaborative approach. We identified 12 trials that randomly assigned patients either to hPTH or placebo or to hPTH or an active comparator and were at least 1 year in duration. Outcomes included change in bone mineral density (BMD), fractures, back pain and adverse events. Two independent reviewers abstracted data on study characteristics and outcomes.
hPTH(1-34) significantly increases lumbar spine BMD, with smaller increases at the femoral neck and total hip. hPTH(1-84) significantly increases lumbar spine BMD. The data show a significant reduction in both vertebral and nonvertebral fractures with hPTH(1-34) in postmenopausal women with previous vertebral fractures. There were no data on fractures comparing the approved dose of hPTH(1-34) with active comparators.
There is Level I evidence that hPTH(1-34) significantly increases BMD at all skeletal sites except the radius and significantly reduces the risk of new vertebral and nonvertebral fractures in postmenopausal women with prior fractures.
人甲状旁腺激素(hPTH)(1-34)于2004年被批准用于治疗严重骨质疏松症。加拿大骨质疏松症临床指南委员会成员对随机对照试验(RCT)进行了系统评价,以评估hPTH对绝经后骨质疏松症女性和男性预防骨折的疗效和安全性。
我们检索了MEDLINE、EMBASE、HTA、《现刊目次》和Cochrane对照试验注册库,以获取1966年至2005年2月发表的数据。采用Cochrane协作方法对RCT进行系统文献检索。我们确定了12项试验,这些试验将患者随机分为hPTH组或安慰剂组,或hPTH组或活性对照剂组,试验持续时间至少为1年。结局包括骨密度(BMD)变化、骨折、背痛和不良事件。两名独立的审阅者提取了关于研究特征和结局的数据。
hPTH(1-34)显著增加腰椎骨密度,股骨颈和全髋骨密度增加幅度较小。hPTH(1-84)显著增加腰椎骨密度。数据显示,对于既往有椎体骨折的绝经后女性,hPTH(1-34)可显著降低椎体和非椎体骨折的发生率。没有关于将hPTH(1-34)的批准剂量与活性对照剂进行骨折比较的数据。
有I级证据表明,hPTH(1-34)可显著增加除桡骨外所有骨骼部位的骨密度,并显著降低既往有骨折的绝经后女性发生新的椎体和非椎体骨折的风险。