骨质疏松症
甲状旁腺激素
成骨细胞
医学
内科学
骨矿物
内分泌学
糖皮质激素
合成代谢
安慰剂
生物信息学
化学
生物
钙
病理
替代医学
生物化学
体外
标识
DOI:10.1016/j.tem.2004.05.005
摘要
A new era in osteoporosis management began with the recent approval of parathyroid hormone (PTH) for postmenopausal and idiopathic osteoporosis treatment. Intermittent PTH dramatically increases spine bone mineral density and significantly reduces fragility fractures. However, the skeletal response to PTH varies greatly and there are few large scale, randomized, placebo-controlled trials in conditions such as glucocorticoid-induced osteoporosis. Moreover, the mechanisms of PTH action are complex, involving multiple pathways linked to common signaling peptides regulating osteoblast gene transcription. In addition, important interactions between osteoclasts and osteoblasts are activated by PTH. This review presents recent findings on PTH signaling in bone and discusses how they could be used to design randomized trials and establish clinical practice guidelines for this novel anabolic peptide.
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