Prevention of incident fractures in patients with prevalent fragility fractures: Current and future approaches

被引:6
作者
Appelman-Dijkstra, Natasha M. [1 ]
Papapoulos, Socrates E. [1 ]
机构
[1] Leiden Univ, Med Ctr, Ctr Bone Qual, NL-2333 ZA Leiden, Netherlands
来源
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2013年 / 27卷 / 06期
关键词
Fractures; Osteoporosis; Bisphosphonates; Denosumab; SERMs; PTH; Strontium ranelate; Cathepsin K; Sclerostin; BONE-MINERAL DENSITY; CATHEPSIN-K INHIBITORS; YEARLY ZOLEDRONIC ACID; VITAMIN-D STATUS; POSTMENOPAUSAL WOMEN; VERTEBRAL FRACTURE; NONVERTEBRAL FRACTURES; STRONTIUM RANELATE; SCLEROSTIN ANTIBODY; PARATHYROID-HORMONE;
D O I
10.1016/j.berh.2014.01.010
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Fragility fractures are a significant, independent risk factor for new fractures, but treatment uptake in subjects with prevalent fractures is disappointing. We addressed the question of the efficacy of pharmacological interventions in reducing the risk of incident fractures in patients with prevalent fragility fractures. For this, we reviewed randomised controlled trials (RCTs), pre-planned and post-hoc analyses of RCTs of approved agents for the treatment of osteoporosis. Results showed that a number of agents decrease the risk of incident vertebral and nonvertebral fractures in subjects with prevalent vertebral fractures, justifying the recommendation of treating such patients independently of the level of bone mineral density (BMD). By contrast, the evidence of antifracture efficacy of these agents in patients with prevalent nonvertebral fractures is limited. Advances in our understanding of the regulation of bone metabolism at the molecular level have identified targets for the development of new therapeutics for osteoporosis, some of which are currently in phase 3 clinical development. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:805 / 820
页数:16
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