一项随机双盲试验,比较特立帕肽[重组人甲状旁腺激素(1-34)]与阿仑膦酸钠对绝经后骨质疏松症女性的疗效。

A randomized double-blind trial to compare the efficacy of teriparatide [recombinant human parathyroid hormone (1-34)] with alendronate in postmenopausal women with osteoporosis.

作者信息

Body Jean-Jacques, Gaich Gregory A, Scheele Wim H, Kulkarni Pandurang M, Miller Paul D, Peretz Anne, Dore Robin K, Correa-Rotter Ricardo, Papaioannou Alexandra, Cumming David C, Hodsman Anthony B

机构信息

Department of Medicine, Institut J. Bordet, Université Libre de Bruxelles, 1000 Brussels, Belgium.

出版信息

J Clin Endocrinol Metab. 2002 Oct;87(10):4528-35. doi: 10.1210/jc.2002-020334.

Abstract

Teriparatide (rDNA origin) injection [recombinant human PTH (1-34)] stimulates bone formation, increases bone mineral density (BMD), and restores bone architecture and integrity. In contrast, bisphosphonates reduce bone resorption and increase BMD. We compared the effects of teriparatide and alendronate sodium on BMD, nonvertebral fracture incidence, and bone turnover in 146 postmenopausal women with osteoporosis. Women were randomized to either once-daily sc injections of teriparatide 40 micro g plus oral placebo (n = 73) or oral alendronate 10 mg plus placebo injection (n = 73). Median duration of treatment was 14 months. At 3 months, teriparatide increased lumbar spine BMD significantly more than did alendronate (P < 0.001). Lumbar spine-BMD increased by 12.2% in the teriparatide group and 5.6% in the alendronate group (P < 0.001 teriparatide vs. alendronate). Teriparatide increased femoral neck BMD and total body bone mineral significantly more than did alendronate, but BMD at the one third distal radius decreased, compared with alendronate (P < or = 0.05). Nonvertebral fracture incidence was significantly lower in the teriparatide group than in the alendronate group (P < 0.05). Both treatments were well tolerated despite transient mild asymptomatic hypercalcemia with teriparatide treatment. In conclusion, teriparatide, a bone formation agent, increased BMD at most sites and decreased nonvertebral fractures more than alendronate.

摘要

特立帕肽(重组DNA来源)注射液[重组人甲状旁腺激素(1-34)]可刺激骨形成,增加骨矿物质密度(BMD),并恢复骨结构和完整性。相比之下,双膦酸盐可减少骨吸收并增加BMD。我们比较了特立帕肽和阿仑膦酸钠对146名绝经后骨质疏松症女性的BMD、非椎体骨折发生率和骨转换的影响。女性被随机分为每日一次皮下注射40μg特立帕肽加口服安慰剂组(n = 73)或口服10mg阿仑膦酸钠加安慰剂注射组(n = 73)。中位治疗持续时间为14个月。3个月时,特立帕肽使腰椎BMD的增加显著高于阿仑膦酸钠(P < 0.001)。特立帕肽组腰椎BMD增加了12.2%,阿仑膦酸钠组增加了5.6%(特立帕肽与阿仑膦酸钠相比,P < 0.001)。特立帕肽使股骨颈BMD和全身骨矿物质的增加显著高于阿仑膦酸钠,但与阿仑膦酸钠相比,桡骨远端三分之一处的BMD降低(P≤0.05)。特立帕肽组的非椎体骨折发生率显著低于阿仑膦酸钠组(P < 0.05)。尽管特立帕肽治疗时有短暂轻度无症状高钙血症,但两种治疗耐受性均良好。总之,作为一种骨形成药物,特立帕肽在大多数部位增加了BMD,并且比阿仑膦酸钠更能减少非椎体骨折。

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