Ng Kong Wah, Martin T John
University of Melbourne, Department of Medicine, St. Vincent's Institute of Medical Research, 9 Princes Street, Fitzroy 3065, Victoria, Australia.
University of Melbourne, Department of Medicine, St. Vincent's Institute of Medical Research, 9 Princes Street, Fitzroy 3065, Victoria, Australia.
Curr Opin Pharmacol. 2014 Jun;16:58-63. doi: 10.1016/j.coph.2014.03.004. Epub 2014 Mar 31.
Two new approaches for the treatment of osteoporosis are summarized, each having arisen out of important new discoveries in bone biology. Odanacatib (ODN) inhibits the enzyme, cathepsin K, that is essential for the resorbing activity of osteoclasts. It is effective in preventing ovariectomy-induced bone loss in preclinical studies, and a phase II clinical study has shown inhibition of resorption sustained over five years. Outcome of a phase III study is awaited. The finding from mouse and human genetics that Wnt signaling is a powerful inducer of bone formation led to developments aimed at enhancing this pathway. Of the several approaches towards this, the most advanced is with a neutralizing antibody against sclerostin, the osteocyte-derived inhibitor of Wnt signaling. Preclinical studies show a powerful bone anabolic effect, and a clinical phase II study shows dose-dependent increases in bone formation and decreases in bone resorption markers.
本文总结了两种治疗骨质疏松症的新方法,每种方法都源于骨生物学领域的重要新发现。奥达卡替(ODN)可抑制组织蛋白酶K,该酶对破骨细胞的吸收活性至关重要。在临床前研究中,它可有效预防卵巢切除引起的骨质流失,一项II期临床研究表明,其对吸收的抑制作用可持续五年。目前正在等待III期研究的结果。小鼠和人类遗传学研究发现,Wnt信号通路是骨形成的强大诱导剂,这促使人们开发旨在增强该通路的方法。在针对此目的的几种方法中,最先进的是使用抗硬化蛋白的中和抗体,硬化蛋白是骨细胞衍生的Wnt信号通路抑制剂。临床前研究显示出强大的骨合成代谢作用,一项II期临床研究表明,骨形成呈剂量依赖性增加,骨吸收标志物减少。