特立帕肽
医学
骨质疏松症
内科学
甲状旁腺激素
骨矿物
内分泌学
维生素D与神经学
骨吸收
钙
作者
Anthony B. Hodsman,Douglas C. Bauer,David W. Dempster,Larry Dian,David A. Hanley,Steven T. Harris,David L. Kendler,Michael R. McClung,Paul D. Miller,Wojciech P. Olszynski,Eric Orwoll,Chui Kin Yuen
出处
期刊:Endocrine Reviews
[The Endocrine Society]
日期:2005-03-15
卷期号:26 (5): 688-703
被引量:693
摘要
All therapies currently recommended for the management of osteoporosis act mainly to inhibit bone resorption and reduce bone remodeling. PTH and its analog, teriparatide [recombinant human PTH(1–34)], represent a new class of anabolic therapies for the treatment of severe osteoporosis, having the potential to improve skeletal microarchitecture. Significant reductions in both vertebral and appendicular fracture rates have been demonstrated in the phase III trial of teriparatide, involving elderly women with at least one prevalent vertebral fracture before the onset of therapy. However, there is as yet no evidence that the antifracture efficacy of PTH will be superior to the bisphosphonates, whereas cost-utility estimates suggest that teriparatide is significantly more expensive.
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