Antiresorptive therapies for osteoporosis: a clinical overview

被引:157
作者
Chen, Jian Sheng [1 ]
Sambrook, Philip N. [1 ]
机构
[1] Univ Sydney, Royal N Shore Hosp, Inst Bone & Joint Res, St Leonards, NSW 2065, Australia
关键词
VERTEBRAL FRACTURE RISK; CORTICOSTEROID-INDUCED OSTEOPOROSIS; ESTABLISHED PRIMARY OSTEOPOROSIS; BONE-MINERAL DENSITY; POSTMENOPAUSAL WOMEN; DOUBLE-BLIND; ZOLEDRONIC ACID; HIP FRACTURE; SECONDARY OSTEOPOROSIS; SALMON-CALCITONIN;
D O I
10.1038/nrendo.2011.146
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Antiresorptive therapies are used to increase bone strength in individuals with osteoporosis and include five principal classes of agents: bisphosphonates, estrogens, selective estrogen receptor modulators (SERMs), calcitonin and monoclonal antibodies such as denosumab. However, no head-to-head studies have compared different antiresorptive agents using fracture as an end point. Bisphosphonates, which have proven antifracture efficacy and a good safety profile, are the most widely used first-line antiresorptive therapy and are recommended for patients with osteoporosis, a prior fragility fracture or osteopenia, as well as individuals with a high risk of fracture. Denosumab, which also has good antifracture efficacy, is another possible first-line therapy, although long-term safety data are lacking. However, no single antiresorptive therapy is currently appropriate for all patients or clearly superior to other therapies. Antiresorptive agents such as estrogens, SERMs (in postmenopausal women) and calcitonin are considered to be second-line agents that are appropriate in special circumstances. Clinicians should determine the most appropriate pharmacological therapy after a careful assessment of the risk:benefit profiles of these drugs in each patient. In addition, patients should receive a detailed explanation of the treatment goals, so that the therapeutic benefit can be maximized through good compliance and persistence.
引用
收藏
页码:81 / 91
页数:11
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