从骨骼健康到寿命:抗骨吸收剂的多效性。

IF 4.2
Endocrinology and metabolism (Seoul, Korea) Pub Date : 2025-08-01 Epub Date: 2025-08-20 DOI:10.3803/EnM.2025.2571
Kyoung Jin Kim
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引用次数: 0

摘要

骨质疏松性骨折是导致发病率和死亡率过高的主要原因,尤其是在老年人中。抗骨吸收药物,包括选择性雌激素受体调节剂(SERMs)、双膦酸盐(bp)和地诺单抗,广泛用于预防骨折,有临床证据的有力支持。除了降低骨折风险外,新出现的数据表明,这些疗法可能通过超出骨骼保护的机制提供生存益处。本综述总结了抗吸收治疗与全因死亡率之间关系的现有证据,整合了随机对照试验和大规模观察队列的研究结果。静脉注射和含氮bp以及denosumab显示出最一致的死亡率降低,特别是在老年人或骨折后人群中。SERMs可能对心血管或肿瘤风险增加的特定妇女提供适度的益处。观察到的死亡率降低可能不仅是由预防骨折介导的,而且是由多种作用介导的,如血管保护、免疫调节、代谢调节和抗癌作用。这些发现强调了认识到骨质疏松是一种全身性疾病的重要性,并支持早期、持续的抗骨吸收治疗,以改善骨骼和生存结果。需要进一步的研究来阐明潜在的机制,并指导不同患者群体的个体化治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

From Bone Health to Lifespan: Pleiotropic Effects of Antiresorptive Agents.

From Bone Health to Lifespan: Pleiotropic Effects of Antiresorptive Agents.

Osteoporotic fractures are a major contributor to morbidity and excess mortality, particularly among older adults. Antiresorptive agents, including selective estrogen receptor modulators (SERMs), bisphosphonates (BPs), and denosumab, are widely used to prevent fractures, with robust support from clinical evidence. Beyond reducing fracture risk, emerging data indicate that these therapies may provide survival benefits through mechanisms that extend beyond skeletal protection. This review summarizes current evidence on the association between antiresorptive therapy and all-cause mortality, integrating findings from randomized controlled trials and large-scale observational cohorts. Intravenous and nitrogen-containing BPs, as well as denosumab, demonstrate the most consistent mortality reduction, especially in older or post-fracture populations. SERMs may provide modest benefits in selected women with increased cardiovascular or oncologic risk. The observed mortality reduction may be mediated not only by fracture prevention but also by pleiotropic effects, such as vascular protection, immune modulation, metabolic regulation, and anti-cancer actions. These findings underscore the importance of recognizing osteoporosis as a systemic disease and support early, sustained antiresorptive treatment to improve both skeletal and survival outcomes. Further studies are needed to clarify the underlying mechanisms and to guide individualized treatment strategies across diverse patient populations.

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