Tabatabai Laila, Cosman Felicia, Curtis Jeffrey R, DeSapri Kristi T, LaBaume Clayton T, Reginster Jean-Yves, Rizzoli René, Cortet Bernard, Wang Yamei, Chiodo Joseph, Mitlak Bruce H
Houston Methodist SPG (Specialty Physician Group), Weill Cornell Medicine, Houston, Texas.
Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York.
Endocr Pract. 2025 Feb;31(2):159-168. doi: 10.1016/j.eprac.2024.10.017. Epub 2024 Nov 16.
Abaloparatide and teriparatide are osteoanabolic treatments indicated for postmenopausal women and men with osteoporosis at high risk of fracture. In the Abaloparatide Comparator Trial In Vertebral Endpoints study, bone mineral density improvements were significantly greater with abaloparatide compared to teriparatide at the total hip and femoral neck. We conducted a retrospective claims study to examine the incidences of hip and nonvertebral fractures and cardiovascular events in women aged ≥50 years initiating abaloparatide or teriparatide therapy, expanding on a previous retrospective claims study.
This retrospective observational study used anonymized claims data from ICON's Symphony Health, PatientSource for women aged ≥ 50 years with ≥ 1 prescription fill for abaloparatide or teriparatide. The index date was the date of the initial prescription dispensed. Times to first hip fracture, nonvertebral fracture, and serious cardiovascular event were compared between logistic regression-based propensity score-matched cohorts and in predefined subgroups by age, prior antiresorptive use, and prior fracture using Cox proportional hazards models.
Patients (21 676 per cohort) were well matched on 73 baseline parameters. Forty-five percent of patients in the abaloparatide arm and 47% in the teriparatide arm were exposed to treatment for longer than 12 months. Over 18 months (+ 30 days follow-up), 245 (1.1%) and 296 (1.4%) women in the abaloparatide and teriparatide cohorts, respectively, had a hip fracture (HR [95% CI] 0.83 [0.70, 0.98]; P = .027); 947 (4.4%) and 1078 (5.0%) had a nonvertebral fracture (0.88 [0.80, 0.96]; P = .003). There were no significant treatment-subgroup interactions (P ≥ .2). Cardiovascular events were similar between groups.
There were significantly lower rates of hip and nonvertebral fractures with abaloparatide compared to teriparatide, which were consistent across subgroups. No differences in cardiovascular safety were noted between cohorts.
阿巴洛肽和特立帕肽是用于治疗绝经后骨质疏松症且骨折风险高的女性和男性的骨合成代谢药物。在阿巴洛肽椎体终点比较试验研究中,与特立帕肽相比,阿巴洛肽在全髋和股骨颈处的骨密度改善显著更大。我们开展了一项回顾性索赔研究,以检查开始使用阿巴洛肽或特立帕肽治疗的≥50岁女性中髋部和非椎体骨折以及心血管事件的发生率,这是对之前一项回顾性索赔研究的扩展。
这项回顾性观察性研究使用了来自艾昆纬公司Symphony Health、PatientSource的匿名索赔数据,这些数据来自年龄≥50岁且至少有1次阿巴洛肽或特立帕肽处方配药记录的女性。索引日期为首次配药的日期。通过基于逻辑回归的倾向评分匹配队列,并使用Cox比例风险模型在按年龄、既往抗吸收药物使用情况和既往骨折情况划分的预定义亚组中,比较首次发生髋部骨折、非椎体骨折和严重心血管事件的时间。
两组患者(每组21676例)在73个基线参数上匹配良好。阿巴洛肽组45%的患者和特立帕肽组47%的患者接受治疗的时间超过12个月。在18个月(+30天随访期)内,阿巴洛肽组和特立帕肽组分别有245例(1.1%)和296例(1.4%)女性发生髋部骨折(风险比[95%置信区间]0.83[0.70,0.98];P = 0.027);947例(4.4%)和1078例(5.0%)发生非椎体骨折(0.88[0.80,0.96];P = 0.003)。治疗亚组间无显著交互作用(P≥0.2)。两组间心血管事件相似。
与特立帕肽相比,阿巴洛肽导致的髋部和非椎体骨折发生率显著更低,且在各亚组中均一致。两组间未观察到心血管安全性方面的差异。