Sung Kyunghun, Ha Jeonghoon
Division of Endocrinology and Metabolism, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
J Bone Metab. 2024 Nov;31(4):335-339. doi: 10.11005/jbm.24.763. Epub 2024 Nov 30.
Romosozumab, which is approved for the treatment of osteoporosis, has a dual-action mechanism that promotes bone formation and inhibits bone resorption. However, its association with an increased risk of major adverse cardiovascular events, as highlighted in the ARCH I study, raises concerns. The underlying pathophysiological mechanisms, possibly involving changes in platelet dynamics, are yet to be fully elucidated. Herein, we present a case of a 60-year-old Korean woman diagnosed with immune thrombocytopenic purpura and new-onset osteoporosis, who was treated with romosozumab. Subsequent to the administration of romosozumab, there was a notable elevation in her platelet count. This observation warrants further investigation into the off-target effects of romosozumab, especially its impact on hematopoietic stem cell function and platelet dynamics. This case accentuates the imperative for more comprehensive research into the systemic effects of romosozumab, particularly its involvement in hematopoiesis and cardiovascular risk, to thoroughly understand its extensive implications for patient health.
罗莫单抗已被批准用于治疗骨质疏松症,它具有促进骨形成和抑制骨吸收的双重作用机制。然而,正如ARCH I研究所强调的,它与主要不良心血管事件风险增加有关,这引发了人们的担忧。其潜在的病理生理机制,可能涉及血小板动力学的变化,尚未完全阐明。在此,我们报告一例60岁韩国女性患者,她被诊断为免疫性血小板减少性紫癜和新发骨质疏松症,并接受了罗莫单抗治疗。在使用罗莫单抗后,她的血小板计数显著升高。这一观察结果值得进一步研究罗莫单抗的脱靶效应,尤其是其对造血干细胞功能和血小板动力学的影响。该病例凸显了对罗莫单抗的全身效应进行更全面研究的必要性,特别是其在造血过程和心血管风险中的作用,以彻底了解其对患者健康的广泛影响。