Prince Richard, Sipos Adrien, Hossain Anwar, Syversen Unni, Ish-Shalom Sophia, Marcinowska Ewa, Halse Johan, Lindsay Robert, Dalsky Gail P, Mitlak Bruce H
Department of Endocrinology and Diabetes and University of Western Australia, Sir Charles Gairdner Hospital, Nedlands, Australia.
J Bone Miner Res. 2005 Sep;20(9):1507-13. doi: 10.1359/JBMR.050501. Epub 2005 May 2.
A follow-up in 1262 women was conducted after the discontinuation of teriparatide. The hazard ratio for combined teriparatide group (20 and 40 microg) for the 50-month period after baseline was 0.57 (p = 0.002), suggesting a sustained effect in reducing the risk of nonvertebral fragility fracture.
Treatment with teriparatide [rhPTH(1-34)] 20 and 40 microg once-daily subcutaneous dosing significantly reduced the risk of nonvertebral fragility fractures over a median exposure of 19 months.
All participants in the Fracture Prevention Trial were invited to participate in a follow-up study. Prior treatment assignments were revealed, and patients were able to receive osteoporosis treatments without restriction.
Approximately 60% of the 1262 patients received an osteoporosis treatment at some time during follow-up, with greater use in the former placebo group than in the combined former teriparatide group (p < 0.05). The hazard ratios for nonvertebral fragility fractures in each teriparatide group relative to placebo were statistically significant for the 50-month period including treatment and follow-up (p < 0.03). In the follow-up period, the hazard ratio was significantly different between the 40 mug and combined groups versus placebo but not for the 20 microg group versus placebo. However, the 20 and 40 microg groups were not different from each other. Kaplan-Meier analysis of time to fracture showed that the fracture incidence in the former placebo and teriparatide groups diverged during the 50-month period including teriparatide treatment and follow-up (p = 0.009). Total hip and femoral neck BMD decreased in teriparatide-treated patients who had no follow-up treatment; BMD remained stable or further increased in patients who received a bisphosphonate after teriparatide treatment.
While the study design is observational, the results support a sustained effect of teriparatide in reducing the risk of nonvertebral fragility fractures up to 30 months after discontinuation of treatment.
在停用特立帕肽后对1262名女性进行了随访。基线后50个月期间,联合特立帕肽组(20微克和40微克)的风险比为0.57(p = 0.002),表明在降低非椎体脆性骨折风险方面有持续效果。
每日一次皮下注射20微克和40微克特立帕肽[重组人甲状旁腺激素(1 - 34)]治疗,在中位暴露时间19个月内显著降低了非椎体脆性骨折的风险。
骨折预防试验的所有参与者均受邀参加一项随访研究。披露了先前的治疗分配情况,患者能够不受限制地接受骨质疏松症治疗。
1262名患者中约60%在随访期间的某个时间接受了骨质疏松症治疗,前安慰剂组的使用量高于联合前特立帕肽组(p < 0.05)。在包括治疗和随访的50个月期间,各特立帕肽组相对于安慰剂的非椎体脆性骨折风险比具有统计学意义(p < 0.03)。在随访期,40微克组和联合组相对于安慰剂的风险比有显著差异,但20微克组相对于安慰剂无差异。然而,20微克组和40微克组之间无差异。骨折时间的Kaplan - Meier分析表明,在前安慰剂组和特立帕肽组中,在包括特立帕肽治疗和随访的50个月期间骨折发生率出现差异(p = 0.009)。未接受后续治疗的特立帕肽治疗患者的全髋和股骨颈骨密度降低;特立帕肽治疗后接受双膦酸盐治疗的患者骨密度保持稳定或进一步增加。
虽然该研究设计为观察性研究,但结果支持特立帕肽在停药后长达30个月内降低非椎体脆性骨折风险的持续效果。