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骨质疏松症治疗的最新进展

Recent Progresses in the Treatment of Osteoporosis.

作者信息

Li Shan-Shan, He Shi-Hao, Xie Peng-Yu, Li Wei, Zhang Xin-Xin, Li Tian-Fang, Li Dai-Feng

机构信息

Department of Rheumatology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Department of Orthopaedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Front Pharmacol. 2021 Jul 22;12:717065. doi: 10.3389/fphar.2021.717065. eCollection 2021.

Abstract

Osteoporosis (OP) is a chronic bone disease characterized by aberrant microstructure and macrostructure of bone, leading to reduced bone mass and increased risk of fragile fractures. Anti-resorptive drugs, especially, bisphosphonates, are currently the treatment of choice in most developing countries. However, they do have limitations and adverse effects, which, to some extent, helped the development of anabolic drugs such as teriparatide and romosozumab. In patients with high or very high risk for fracture, sequential or combined therapies may be considered with the initial drugs being anabolic agents. Great endeavors have been made to find next generation drugs with maximal efficacy and minimal toxicity, and improved understanding of the role of different signaling pathways and their crosstalk in the pathogenesis of OP may help achieve this goal. Our review focused on recent progress with regards to the drug development by modification of Wnt pathway, while other pathways/molecules were also discussed briefly. In addition, new observations made in recent years in bone biology were summarized and discussed for the treatment of OP.

摘要

骨质疏松症(OP)是一种慢性骨病,其特征是骨的微观结构和宏观结构异常,导致骨量减少和脆性骨折风险增加。抗吸收药物,尤其是双膦酸盐类药物,目前是大多数发展中国家的首选治疗药物。然而,它们确实存在局限性和不良反应,这在一定程度上推动了诸如特立帕肽和罗莫单抗等促合成代谢药物的发展。对于骨折高风险或极高风险的患者,可考虑采用序贯或联合治疗,初始药物为促合成代谢药物。人们一直在努力寻找疗效最大化和毒性最小化的下一代药物,而对不同信号通路及其相互作用在OP发病机制中的作用有更深入的了解可能有助于实现这一目标。我们的综述重点关注了通过修饰Wnt通路进行药物研发的最新进展,同时也简要讨论了其他通路/分子。此外,还总结并讨论了近年来在骨生物学方面的新发现,以用于OP的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/8339209/b7d539ab82fd/fphar-12-717065-g001.jpg

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