Rheumatology Department, University of Verona, Valeggio Sul MincioHospital VR, Verona, Italy.
Curr Med Res Opin. 2008 Nov;24(11):3259-74. doi: 10.1185/03007990802518130. Epub 2008 Oct 20.
To review and analyse the evidence supporting the use of full length parathyroid hormone, PTH(1-84), in the treatment of osteoporosis based on a search of several literature sources; articles selected for review were published between 1990 and 2008.
PTH(1-84) is approved for the treatment of osteoporosis in postmenopausal women at high risk of fracture in Europe. It was well tolerated in clinical trials and demonstrated bone building properties and fracture prevention particularly for the lumbar spine in the treatment of postmenopausal women.
The TOP clinical trial showed that PTH(1-84) treatment for 18 months resulted in a 61% reduction (p = 0.001) in new vertebral fracture incidence when compared with placebo and reduced the risk of a first vertebral fracture by 68% (p = 0.006) in women without a prevalent fracture at baseline. PTH(1-84) increased bone mineral density (BMD) at vertebral and non-vertebral sites the lumbar spine BMD increasing regardless of T-score, age, prior osteoporosis therapy or number of years post-menopause. The PaTH study showed that treatment with PTH(1-84) for 12 months increased BMD at the trabecular spine and hip. Lumbar spine BMD gains were largest with sequential administration of PTH(1-84) followed by alendronate but were smaller with concurrent administration involving anabolic and antiresorptive agents. Lumbar spine BMD increases were also seen in trials involving PTH with raloxifene and PTH in combination with hormone replacement therapy.
PTH(1-84) has demonstrated effective bone building qualities and extends the therapeutic options available to osteoporotic women. The use of PTH(1-84) followed by sequential administration of an antiresorptive has proved effective at increasing trabecular BMD and points towards new treatment regimens offering improvements in BMD and fracture prevention.
通过对 1990 年至 2008 年出版的文献进行检索,回顾和分析支持使用全长甲状旁腺激素(PTH[1-84])治疗骨质疏松症的证据。
在欧洲,PTH[1-84]被批准用于治疗有骨折高风险的绝经后骨质疏松症女性。在临床试验中,它具有良好的耐受性,并显示出骨形成特性和预防骨折的作用,特别是对绝经后女性的腰椎。
TOP 临床试验表明,与安慰剂相比,PTH[1-84]治疗 18 个月可使新发椎体骨折发生率降低 61%(p=0.001),且基线时无椎体骨折的女性首次椎体骨折风险降低 68%(p=0.006)。PTH[1-84]增加了椎体和非椎体部位的骨密度,无论 T 评分、年龄、既往骨质疏松症治疗或绝经后年数如何,腰椎骨密度均增加。PaTH 研究表明,PTH[1-84]治疗 12 个月可增加小梁脊柱和髋部的骨密度。与同时使用合成代谢和抗吸收剂相比,连续给予 PTH[1-84]后再给予阿仑膦酸钠可使腰椎骨密度增加最大,但与同时使用合成代谢和抗吸收剂相比,其增加较小。在涉及与雷洛昔芬联合使用的 PTH 和与激素替代疗法联合使用的 PTH 的试验中,也观察到腰椎骨密度增加。
PTH[1-84]已显示出有效的骨形成特性,并扩展了可供骨质疏松症女性选择的治疗方案。使用 PTH[1-84]后再连续使用抗吸收剂已被证明可有效增加小梁骨密度,并指出新的治疗方案可改善骨密度和预防骨折。