Department of Spinal Surgery, The 6th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, 518052, Guangdong, China.
Department of Orthopedics & Orthopedic Institute, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Aging Clin Exp Res. 2023 Mar;35(3):531-539. doi: 10.1007/s40520-023-02342-w. Epub 2023 Jan 28.
Percutaneous vertebroplasty was the most common strategy for osteoporotic vertebral compression fracture. However, refracture after vertebroplasty also occurred and bone mineral density (BMD) was one of the main factors associated with refracture after percutaneous vertebroplasty.
To investigate the efficacy of a short-sequential treatment of teriparatide followed by alendronate on prevention of refracture after percutaneous vertebroplasty in osteoporotic patients, and compare it with the therapy of alendronate alone.
From January 2018 to January 2020, we recruited 165 female osteoporosis patients after percutaneous vertebroplasty who were assigned into sequential treatment of teriparatide followed by alendronate group (TPTD + ALN group) and alendronate alone group (ALN group). The vertebral fracture occurred during this process was also recorded in both the groups. A total of 105 participants completed the 1-year follow-up. Furthermore, BMD and serum procollagen type I N-terminal propeptide (PINP) and C-terminal cross-linking telopeptide of type I collagen (CTX) were compared between the two groups during 1-year follow-up.
The 105 patients were finally included, with 59 in ALN group and 46 in TPTD + ALN group. During 1-year follow-up, the vertebral refracture rate in TPTD + ALN group was much lower than that in ALN group (2.2% vs. 13.6%, p < 0.05). At 12 months, the BMDs at lumbar in TPTD + ALN group were significantly elevated when compared to the ALN group (0.65 ± 0.10 vs. 0.57 ± 0.07, p < 0.001).
A short-sequential administration of teriparatide followed by alendronate was more effective in elevating the BMD and decreasing the refracture rate at 12-month follow-up, compared to the counterpart with alendronate alone.
经皮椎体成形术是治疗骨质疏松性椎体压缩骨折最常用的策略。然而,椎体成形术后也会发生再骨折,骨密度(BMD)是与经皮椎体成形术后再骨折相关的主要因素之一。
探讨特立帕肽序贯阿仑膦酸钠短程治疗对预防骨质疏松性椎体成形术后再骨折的疗效,并与单独使用阿仑膦酸钠进行比较。
自 2018 年 1 月至 2020 年 1 月,我们招募了 165 名经皮椎体成形术后的女性骨质疏松症患者,将其分为特立帕肽序贯阿仑膦酸钠组(TPTD+ALN 组)和单独使用阿仑膦酸钠组(ALN 组)。两组均记录在此过程中发生的椎体骨折情况。共有 105 名参与者完成了 1 年的随访。此外,在 1 年的随访期间,比较了两组患者的骨密度和血清Ⅰ型前胶原氨基端前肽(PINP)和Ⅰ型胶原 C 端交联肽(CTX)。
最终纳入 105 例患者,其中 ALN 组 59 例,TPTD+ALN 组 46 例。在 1 年的随访期间,TPTD+ALN 组的椎体再骨折率明显低于 ALN 组(2.2%比 13.6%,p<0.05)。12 个月时,TPTD+ALN 组的腰椎骨密度明显高于 ALN 组(0.65±0.10 比 0.57±0.07,p<0.001)。
与单独使用阿仑膦酸钠相比,特立帕肽序贯阿仑膦酸钠短程治疗在提高 BMD 和降低 12 个月时的再骨折率方面更有效。