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骨质疏松症治疗方法概述。

Overview of treatment approaches to osteoporosis.

机构信息

Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Br J Pharmacol. 2021 May;178(9):1891-1906. doi: 10.1111/bph.15024. Epub 2020 Mar 20.

Abstract

Efficient therapies are available for the treatment of osteoporosis. Anti-resorptive therapies, including bisphosphonates and denosumab, increase bone mineral density (BMD) and reduce the risk of fractures by 20-70%. Bone-forming or dual-action treatments stimulate bone formation and increase BMD more than the anti-resorptive therapies. Two studies have demonstrated that these treatments are superior to anti-resorptives in preventing fractures in patients with severe osteoporosis. Bone-forming or dual-action treatments should be followed by anti-resorptive treatment to maintain the fracture risk reduction. The BMD gains seen with bone-forming and dual-action treatments are greater in treatment-naïve patients compared to patients pretreated with anti-resorptive treatments. However, the antifracture efficacy seems to be preserved. Treatment failure will often lead to switch of treatment from orally to parentally administrated anti-resorptives treatment or from anti-resorptive to bone-forming or dual-action treatment. Osteoporosis is a chronic condition and therefore needs a long-term management plan with a personalized approach to treatment. LINKED ARTICLES: This article is part of a themed issue on The molecular pharmacology of bone and cancer-related bone diseases. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v178.9/issuetoc.

摘要

治疗骨质疏松症有有效的疗法。抗吸收疗法,包括双磷酸盐和地舒单抗,可增加骨密度(BMD)并降低 20-70%的骨折风险。成骨或双重作用的治疗方法可刺激骨形成并增加 BMD,比抗吸收疗法更有效。两项研究表明,这些治疗方法在预防严重骨质疏松症患者骨折方面优于抗吸收疗法。成骨或双重作用的治疗方法后应进行抗吸收治疗以维持骨折风险降低。与预先接受抗吸收治疗的患者相比,治疗初治患者的成骨和双重作用治疗的 BMD 增加更大。然而,抗骨折疗效似乎得以保留。治疗失败通常会导致从口服抗吸收治疗转为肠外抗吸收治疗,或从抗吸收治疗转为成骨或双重作用治疗。骨质疏松症是一种慢性疾病,因此需要采用个体化的治疗方法制定长期管理计划。

相关文章

本文是骨和癌症相关骨疾病的分子药理学主题问题的一部分。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v178.9/issuetoc.

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