德诺苏马布
医学
骨质疏松症
特立帕肽
双膦酸盐
合成代谢剂
骨密度保护剂
重症监护医学
骨重建
颌骨骨坏死
生物信息学
骨密度
内科学
骨矿物
生物
出处
期刊:PubMed
日期:2015-01-01
卷期号:25 (1): 105-13
被引量:5
摘要
The target to treat osteoporosis is prevention for future fractures. After the evaluation of cathepsin K inhibitors (CKIs) which was developed as antresorptive agents, there is evidence that these agents also possess anabolic activity, suggesting that CKIs differ from so called antiresorptive agents such as bisphosphonates and denosumab. The classification of agents for treatment of osteoporosis has been changed. Bisphosphonate-Related Osteonecrosis of the Jaw (BRONJ) and Atypical femoral fractures (AFFs) have been the problems when the therapy continues relatively for a long period. However, there is no clear guidance on when fracture risk has been reduced to an acceptably low level. As a consequence, some patients at low risk for fracture may be treated for longer than necessary, whereas others at high risk for fracture may have treatment stopped when they might benefit from continuation of the same treatment or a change to a more potent therapeutic agent. Therefore, a "treat-to-target" strategy for the management of patients with osteoporosis has been developed to describe the potential clinical utility of evaluating changes bone density and bone turnover markers, and events of fractures.
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