Prasad Trupti N, Flora Sandeep Singh, Bhadada Sanjay K, Yadav Urmila, Pal Rimesh
Department of Endocrinology, Postgraduate Institute of Medical Education and Research, Chandigarh, India, 160012.
Staff Clinic, Postgraduate Institute of Medical Education and Research, Chandigarh, India, 160012.
Osteoporos Int. 2025 Jun 30. doi: 10.1007/s00198-025-07599-7.
Zoledronate, denosumab and teriparatide improve Falls Risk Assessment Score (FRAS) and reduce the number of participants experiencing falls over the last 12 months when administered over a period of 72 weeks to postmenopausal women with type 2 diabetes mellitus at a high risk of fragility fractures.
Type 2 diabetes mellitus (T2D) increases the risk of falls, which also exacerbates the risk of fragility fractures. We aimed at exploring the effects of anti-osteoporotic therapies (zoledronate, denosumab or teriparatide) on the risk of falls in postmenopausal women with T2D.
We performed an exploratory analysis of a randomized clinical pilot trial primarily designed to compare the efficacy of zoledronate, denosumab, or teriparatide in T2D (CTRI/2022/02/039978). Postmenopausal women (≥ 50 years) with T2D and high risk of fragility fractures were randomized to receive zoledronate (5 mg annually), denosumab (60 mg bi-annually), teriparatide (20 mcg daily) or only standard of care (calcium and cholecalciferol) for 72 weeks. The risk of falls was assessed using FRAS (Falls Risk Assessment Score) questionnaire at baseline and 72 weeks.
129 postmenopausal women were randomized to one of the four treatment arms (mean age 64.2 ± 6.7 years). The baseline characteristics including FRAS were matched between four arms. At 72 weeks, all three interventions led to a significant reduction in FRAS (p = 0.002 for teriparatide, p = 0.004 for zoledronate, p = 0.004 for denosumab). No improvement was observed in control arm (p = 0.875). The number of participants experiencing more than one fall in last 12 months reduced in teriparatide, zoledronate and denosumab arms, while it increased in control arm (between-group p = 0.033). Glycemic status, renal function, calcium and vitamin D status either remained unchanged over 72 weeks or did not correlate with change in FRAS.
Zoledronate, denosumab and teriparatide reduce the risk of falls that might contribute to their anti-fracture efficacy.
对于有脆性骨折高风险的绝经后2型糖尿病女性,唑来膦酸、地诺单抗和特立帕肽在72周的给药期内可改善跌倒风险评估评分(FRAS),并减少过去12个月内发生跌倒的参与者数量。
2型糖尿病(T2D)会增加跌倒风险,这也会加剧脆性骨折的风险。我们旨在探讨抗骨质疏松治疗(唑来膦酸、地诺单抗或特立帕肽)对绝经后T2D女性跌倒风险的影响。
我们对一项随机临床试验进行了探索性分析,该试验主要设计用于比较唑来膦酸、地诺单抗或特立帕肽在T2D中的疗效(CTRI/2022/02/039978)。将有T2D且有脆性骨折高风险的绝经后女性(≥50岁)随机分为接受唑来膦酸(每年5毫克)、地诺单抗(每半年60毫克)、特立帕肽(每日20微克)或仅接受标准治疗(钙和胆钙化醇),为期72周。在基线和72周时使用FRAS(跌倒风险评估评分)问卷评估跌倒风险。
129名绝经后女性被随机分配到四个治疗组之一(平均年龄64.2±6.7岁)。四个组之间包括FRAS在内的基线特征相匹配。在72周时,所有三种干预措施均导致FRAS显著降低(特立帕肽p = 0.002,唑来膦酸p = 0.004,地诺单抗p = 0.004)。对照组未观察到改善(p = 0.875)。在特立帕肽、唑来膦酸和地诺单抗组中,过去12个月内发生不止一次跌倒的参与者数量减少,而对照组中则增加(组间p = 0.033)。血糖状态、肾功能、钙和维生素D状态在72周内要么保持不变,要么与FRAS的变化无关。
唑来膦酸、地诺单抗和特立帕肽可降低跌倒风险,这可能有助于它们的抗骨折疗效。