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2020年骨质疏松症治疗学

Osteoporosis Therapeutics 2020.

作者信息

Kocijan Roland, Klaushofer Klaus, Misof Barbara M

机构信息

Ludwig Boltzmann Institute of Osteology at Hanusch Hospital of OEGK and AUVA Trauma Centre Meidling, 1st Med. Dept. Hanusch Hospital, Vienna, Austria.

出版信息

Handb Exp Pharmacol. 2020;262:397-422. doi: 10.1007/164_2020_373.

Abstract

Numerous safe and efficient drug therapies are currently available to decrease risk of low trauma fractures in patients with osteoporosis including postmenopausal, male, and secondary osteoporosis. In this chapter, we give first an overview of the most important outcomes regarding fracture risk reduction, change in bone mineral density (BMD by DXA) and/or bone markers of the phase III clinical studies of well-established therapies (such as Bisphosphonates, Denosumab or Teriparatide) and also novel therapies (such as Romosozumab or Abaloparatide) and highlight their mechanisms of action at bone tissue/material level. The latter understanding is not only essential for the choice of drug, duration and discontinuation of treatment but also for the interpretation of the clinical outcomes (in particular of eventual changes in BMD) after drug administration. In the second part of this chapter, we focus on the management of different forms of osteoporosis and give a review of the respective current guidelines for treatment. Adverse effects of treatment such as atypical femoral fractures, osteonecrosis of the jaw or influence of fracture healing are considered also in this context.

摘要

目前有许多安全有效的药物疗法可降低骨质疏松症患者低创伤骨折的风险,这些患者包括绝经后骨质疏松症患者、男性骨质疏松症患者以及继发性骨质疏松症患者。在本章中,我们首先概述已确立疗法(如双膦酸盐、地诺单抗或特立帕肽)以及新型疗法(如罗莫单抗或阿巴洛肽)的III期临床研究在降低骨折风险、骨密度(通过双能X线吸收法测定的BMD)变化和/或骨标志物方面的最重要结果,并着重介绍它们在骨组织/材料水平的作用机制。对后者的理解不仅对于药物选择、治疗持续时间和停药至关重要,而且对于药物给药后临床结果(特别是骨密度的最终变化)的解释也至关重要。在本章的第二部分,我们重点关注不同类型骨质疏松症的管理,并综述各自当前的治疗指南。在此背景下,还会考虑治疗的不良反应比如非典型股骨骨折、颌骨坏死或对骨折愈合的影响。

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