Wei Fei-Long, Gao Quan-You, Zhu Kai-Long, Heng Wei, Du Ming-Rui, Yang Fan, Gao Hao-Ran, Li Tian, Qian Ji-Xian, Zhou Cheng-Pei
Department of Orthopaedics, Tangdu Hospital, Fourth Military Medical University, 710038, Xi'an, China.
School of Basic Medicine, Fourth Military Medical University, 710032 Xi'an, China.
Heliyon. 2022 Nov 29;9(2):e11880. doi: 10.1016/j.heliyon.2022.e11880. eCollection 2023 Feb.
There are many pharmaceutical interventions available to prevent osteoporotic vertebral fractures in postmenopausal women, but the efficacy and safety of these drugs are unknown. This study aimed to investigate the efficacy and safety of drugs in the prevention of osteoporotic vertebral fractures.
PubMed, Embase, and the Cochrane Library were comprehensively searched for randomized controlled trials (RCTs) published up to February 15, 2020, including postmenopausal women with osteoporosis. Network meta-analysis was conducted based on the Cochrane Handbook for Systematic Reviews of Interventions and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. The relative risk (RR) and 95% confidence interval (CI) were used to report the results. This study was registered with PROSPERO, number CRD42020201167. Main Outcomes were incidences of new vertebral fracture and serious adverse events.
Fifty-five RCTs (n = 104 580) evaluating vertebral fractures of sixteen kinds of pharmacologic therapies were included in the network meta-analysis. Abaloparatide (RR, 0.21; [95% CI, 0.09 to 0.51]), alendronate (RR, 0.55; [95% CI, 0.38 to 0.81]), calcitonin (RR, 0.44; [95% CI, 0.25 to 0.78]), denosumab (RR, 0.33; [95% CI, 0.14 to 0.61]), parathyroid hormone (PTH) (RR, 0.32; [95% CI, 0.10 to 0.97]), risedronate (RR, 0.65; [95% CI, 0.42 to 1.00]), romosozumab (RR, 0.31; [95% CI, 0.16 to 0.61]), strontium ranelate (RR, 0.62; [95% CI, 0.42 to 0.93]), teriparatide (RR, 0.27; [95% CI, 0.17 to 0.43]), and zoledronate (RR, 0.41; [95% CI, 0.93]) were associated with lower vertebral fracture risk compared to placebo. PTH was associated with more adverse event rates. For any two drug treatments, the RR of serious adverse events was not statistically significant. Hormone replacement therapy (HRT) and calcitonin may be slower to work because they have only been shown to reduce the risk of vertebral fractures in long-term (>18 months) follow-up.
A variety of drugs are safe and effective in preventing osteoporotic vertebral fractures. HRT and calcitonin only reduced the risk of vertebral fractures during a follow-up of 21-72 months.
有多种药物干预措施可用于预防绝经后女性骨质疏松性椎体骨折,但这些药物的疗效和安全性尚不清楚。本研究旨在调查药物预防骨质疏松性椎体骨折的疗效和安全性。
全面检索了截至2020年2月15日发表的随机对照试验(RCT),包括患有骨质疏松症的绝经后女性,检索数据库有PubMed、Embase和Cochrane图书馆。基于《Cochrane系统评价干预措施手册》和系统评价与Meta分析的首选报告项目(PRISMA)指南进行网状Meta分析。采用相对风险(RR)和95%置信区间(CI)报告结果。本研究已在国际前瞻性注册系统(PROSPERO)注册,注册号为CRD42020201167。主要结局为新发椎体骨折和严重不良事件的发生率。
网状Meta分析纳入了55项评估16种药物治疗椎体骨折的随机对照试验(n = 104580)。与安慰剂相比,阿巴洛肽(RR,0.21;[95%CI,0.09至0.51])、阿仑膦酸钠(RR,0.55;[95%CI,0.38至0.81])、降钙素(RR,0.44;[95%CI,0.25至0.78])、地诺单抗(RR,0.33;[95%CI,0.14至0.61])、甲状旁腺激素(PTH)(RR,0.32;[95%CI,0.10至0.97])、利塞膦酸钠(RR,0.65;[95%CI,0.42至1.00])、罗莫佐单抗(RR,0.31;[95%CI,0.16至0.61])、雷奈酸锶(RR,0.62;[95%CI,0.42至0.93])、特立帕肽(RR,0.27;[95%CI,0.17至0.43])和唑来膦酸(RR,0.41;[95%CI,0.93])与较低的椎体骨折风险相关。PTH与更多的不良事件发生率相关。对于任何两种药物治疗,严重不良事件的RR无统计学意义。激素替代疗法(HRT)和降钙素起效可能较慢,因为它们仅在长期(>18个月)随访中显示可降低椎体骨折风险。
多种药物在预防骨质疏松性椎体骨折方面安全有效。HRT和降钙素仅在21 - 72个月的随访期间降低了椎体骨折风险。