Bone biology, signaling pathways, and therapeutic targets for osteoporosis

被引:88
作者
Iniguez-Ariza, Nicole M. [1 ]
Clarke, Bart L. [1 ]
机构
[1] Mayo Clin E18 A, Rochester, MN 55905 USA
关键词
Osteoporosis; Cathepsin K inhibitors; Anti-sclerostin antibody; Anti-Dickkopf antibody; PTH; PTHrP; CATHEPSIN K INHIBITOR; SENSING RECEPTOR ANTAGONIST; PARATHYROID-HORMONE; 1-34; POSTMENOPAUSAL WOMEN; MINERAL DENSITY; SCLEROSTIN ANTIBODY; BIOCHEMICAL MARKERS; CELL BIOLOGY; DOUBLE-BLIND; WNT;
D O I
10.1016/j.maturitas.2015.07.003
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Major advances have occurred recently in the treatment of osteoporosis in recent years. Most patients are currently treated with bisphosphonates, denosumab, raloxifene, or teriparatide, and in some countries, strontium ranelate. Strontium ranelate and calcitonin have recently had their use restricted due to cardiovascular concerns and malignancy, respectively. The available agents have generally provided excellent options that effectively reduce fracture risk. New targets are being sought based on appreciation of the bone biology and signaling pathways involved in bone formation and resorption. These agents will directly target these signaling pathways, and further expand the options available for treatment of osteoporosis. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:245 / +
页数:15
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