Liu Chun-Lin, Lee Han-Chung, Chen Chun-Chung, Cho Der-Yang
Department of Neurosurgery, Neuropsychiatric Center, China Medical University Hospital; Graduate Institute of Medicine, China Medical University.
Clin Invest Med. 2017 Jun 26;40(3):E146-E157. doi: 10.25011/cim.v40i3.28394.
This meta-analysis aimed to compare the efficacy and safety of teriparatide vs. bisphosphonates in the management of osteoporosis.
A total of 1,967 patients from eight randomized controlled trials were analyzed; outcomes included bone mineral density (BMD) of the femoral neck, total hip and lumbar spine, vertebral and nonvertebral fractures and any adverse event. A subgroup analysis of treatment effectiveness was performed according to the etiology of osteoporosis; i.e., glucocorticoid-induced osteoporosis (GIO) vs. post-menopausal osteoporosis (PO).
Teriparatide increased the BMD of the lumbar spine, femoral neck and total hip to a greater extent than bisphosphonates. Patients treated with teriparatide also had a lower risk of vertebral fractures compared with bisphosphonates; however, no difference in risk of nonvertebral fractures (or adverse events) was found. GIO subgroups showed larger increases in BMD of the lumbar spine, total hip and femoral neck in patients treated with teriparatide compared with bisphosphonates. The PO subgroup showed larger increases in BMD of the lumbar spine in patients treated with teriparatide compared with bisphosphonates. Patients in the GIO subgroup (but not the PO subgroup) were less likely to suffer a vertebral fracture on teriparatide as compared with bisphosphonates. In contrast, no significant difference in the percentage of nonvertebral fractures was noted between the two types of treatment for either subgroup.
Teriparatide significantly increased the BMD of lumbar spine, total hip and femoral neck, particularly in GIO-induced osteoporosis. Teriparatide did not lower the risk of nonvertebral fractures when compared with bisphosphonates.
本荟萃分析旨在比较特立帕肽与双膦酸盐类药物在骨质疏松症治疗中的疗效和安全性。
对来自八项随机对照试验的1967例患者进行分析;结局指标包括股骨颈、全髋和腰椎的骨密度(BMD)、椎体和非椎体骨折以及任何不良事件。根据骨质疏松症的病因进行治疗效果的亚组分析;即糖皮质激素诱导的骨质疏松症(GIO)与绝经后骨质疏松症(PO)。
与双膦酸盐类药物相比,特立帕肽能更大程度地提高腰椎、股骨颈和全髋的骨密度。与双膦酸盐类药物相比,接受特立帕肽治疗的患者发生椎体骨折的风险也更低;然而,未发现非椎体骨折(或不良事件)风险存在差异。与双膦酸盐类药物相比,GIO亚组中接受特立帕肽治疗的患者腰椎、全髋和股骨颈的骨密度增加幅度更大。与双膦酸盐类药物相比,PO亚组中接受特立帕肽治疗的患者腰椎骨密度增加幅度更大。与双膦酸盐类药物相比,GIO亚组(而非PO亚组)的患者使用特立帕肽时发生椎体骨折的可能性更小。相比之下,两个亚组的两种治疗方法在非椎体骨折发生率方面均未发现显著差异。
特立帕肽能显著提高腰椎、全髋和股骨颈的骨密度,尤其是在GIO所致的骨质疏松症中。与双膦酸盐类药物相比,特立帕肽并未降低非椎体骨折的风险。