Arcidiacono Gaetano Paride, Campello Elena, Simion Chiara, Giannini Sandro, Simioni Paolo
Department of Medicine (DIMED), University of Padova, Padova, Italy; First Chair of Internal Medicine, University Hospital of Padova, Padova, Italy.
Department of Medicine (DIMED), University of Padova, Padova, Italy; First Chair of Internal Medicine, University Hospital of Padova, Padova, Italy.
J Thromb Haemost. 2025 Nov;23(11):3424-3436. doi: 10.1016/j.jtha.2025.07.037. Epub 2025 Aug 20.
Hemostasis and bone metabolism, traditionally considered as distinct physiological systems, are now recognized to share a complex and bidirectional interplay. Emerging evidence reveals that several components of the hemostatic cascade-including coagulation factors and platelets-may modulate bone cell function and remodeling. Conversely, key regulators of bone and mineral metabolism, such as calcium, vitamin D, and parathyroid hormone, exert significant effects on vascular and hemostatic pathways. This interplay is especially relevant in aging populations, where the incidence of thrombotic disorders and skeletal fragility increases, and the 2 conditions often coexist, with long-term use of anticoagulants or osteoporosis therapies potentially affecting both systems. In this narrative review, we synthesize current insights into the molecular and cellular mechanisms involved in the hemostasis-bone interaction. We also discuss how disorders of mineral metabolism influence coagulation and, conversely, how hemostatic conditions may affect skeletal health. Moreover, we examine how pharmacologic agents-such as anticoagulants and osteoporosis therapies-may impact the hemostasis-bone axis. While most available evidence is preclinical or observational, emerging data point to potential clinical implications that warrant further investigation. A deeper understanding of this interplay could support more effective therapeutic strategies and improve risk assessment in patients with concurrent coagulation and skeletal disorders.
止血与骨代谢,传统上被视为不同的生理系统,如今人们认识到它们之间存在复杂的双向相互作用。新出现的证据表明,止血级联反应的几个组成部分,包括凝血因子和血小板,可能会调节骨细胞功能和重塑。相反,骨与矿物质代谢的关键调节因子,如钙、维生素D和甲状旁腺激素,对血管和止血途径有显著影响。这种相互作用在老年人群中尤为重要,在这一人群中,血栓形成性疾病和骨骼脆弱的发生率增加,而且这两种情况常常同时存在,长期使用抗凝剂或骨质疏松症治疗方法可能会对这两个系统产生影响。在这篇叙述性综述中,我们综合了目前对止血与骨相互作用所涉及的分子和细胞机制的见解。我们还讨论了矿物质代谢紊乱如何影响凝血,反之,止血情况又如何影响骨骼健康。此外,我们研究了诸如抗凝剂和骨质疏松症治疗药物等药物可能如何影响止血-骨轴。虽然大多数现有证据是临床前或观察性的,但新出现的数据指出了潜在的临床意义,值得进一步研究。对这种相互作用的更深入理解可以支持更有效的治疗策略,并改善同时患有凝血和骨骼疾病患者的风险评估。