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生成骨质以逆转骨质疏松并修复骨折。

Building bone to reverse osteoporosis and repair fractures.

作者信息

Khosla Sundeep, Westendorf Jennifer J, Oursler Merry Jo

机构信息

Endocrine Research Unit, College of Medicine, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

J Clin Invest. 2008 Feb;118(2):421-8. doi: 10.1172/JCI33612.

Abstract

An important, unfilled clinical need is the development of new approaches to improve fracture healing and to treat osteoporosis by increasing bone mass. Recombinant forms of bone morphogenetic protein 2 (BMP2) and BMP7 are FDA approved to promote spinal fusion and fracture healing, respectively, and the first FDA-approved anabolic drug for osteoporosis, parathyroid hormone, increases bone mass when administered intermittently but can only be given to patients in the US for two years. As we discuss here, the tremendous explosion over the last two decades in our fundamental understanding of the mechanisms of bone remodeling has led to the prospect of mechanism-based anabolic therapies for bone disorders.

摘要

一个重要的、尚未满足的临床需求是开发新方法来改善骨折愈合以及通过增加骨量来治疗骨质疏松症。重组骨形态发生蛋白2(BMP2)和BMP7分别获得美国食品药品监督管理局(FDA)批准用于促进脊柱融合和骨折愈合,而首个获FDA批准用于治疗骨质疏松症的促合成代谢药物甲状旁腺激素,间歇性给药时可增加骨量,但仅能在美国给患者使用两年。正如我们在此所讨论的,在过去二十年里,我们对骨重塑机制的基本认识有了巨大飞跃,这带来了基于机制的骨疾病促合成代谢疗法的前景。

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