Tsur Anat, Cahn Avivit, Levy Ludmila, Pollack Rena
Department of Endocrinology and Metabolism, Clalit Health Services, Jerusalem 9310609, Israel.
The Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem 9112102, Israel.
JBMR Plus. 2024 Dec 10;9(1):ziae146. doi: 10.1093/jbmrpl/ziae146. eCollection 2025 Jan.
Romosozumab is a potent treatment for osteoporosis, with significant effects on bone density and fracture prevention. This study evaluated the cardiovascular safety of romosozumab in a real-world cohort of postmenopausal women at high fracture risk. We retrospectively evaluated postmenopausal women who initiated treatment with romosozumab between January 1, 2020, and June 30, 2023. We examined the occurrence of a major adverse cardiovascular event (MACE) across two distinct segments during the treatment period and after its conclusion. After applying inclusion and exclusion criteria, 847 women were followed for a median of 729 days (IQR: 445-1060). The incidence rate of MACE was 24.0 (95% CI 17.7-32.5) per 1000 person-years during the study period. The change in the rate of MACE from 0-90 days and 90-365 days post-treatment initiation was 0.04 and 0.06 events per 1000 days, respectively. The difference in the rate between these intervals was not statistically significant ( = .09). After 1 yr of treatment, the slope of MACE increased to 0.10, differing significantly from the preceding 12 mo on treatment (<.001). The incidence of MACE was higher in those with a background of previous cardiovascular disease or diabetes at all timepoints, as expected. The consistency in event rates during treatment suggests that romosozumab is not associated with an increase in MACE in postmenopausal women. This finding challenges reports suggesting an increase in cardiovascular events within the first year of romosozumab treatment.
罗莫佐单抗是一种有效的骨质疏松症治疗药物,对骨密度和骨折预防有显著效果。本研究评估了罗莫佐单抗在骨折高风险绝经后女性真实世界队列中的心血管安全性。我们回顾性评估了在2020年1月1日至2023年6月30日期间开始使用罗莫佐单抗治疗的绝经后女性。我们检查了治疗期间及结束后两个不同时间段内主要不良心血管事件(MACE)的发生情况。应用纳入和排除标准后,对847名女性进行了中位729天(四分位间距:445 - 1060)的随访。研究期间MACE的发病率为每1000人年24.0(95%置信区间17.7 - 32.5)。治疗开始后0 - 90天和90 - 365天MACE发生率的变化分别为每1000天0.04和0.06例事件。这些时间段之间发生率的差异无统计学意义(P = 0.09)。治疗1年后,MACE的斜率增至0.10,与治疗前12个月显著不同(P < 0.001)。正如预期的那样,在所有时间点,有既往心血管疾病或糖尿病背景的患者MACE发生率更高。治疗期间事件发生率的一致性表明,罗莫佐单抗与绝经后女性MACE增加无关。这一发现对有关罗莫佐单抗治疗第一年中心血管事件增加的报道提出了挑战。