预防脊髓损伤骨质疏松症(POPSCI)研究--急性脊髓损伤患者早期输注唑来膦酸。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-11-01 Epub Date: 2024-09-25 DOI:10.1007/s00223-024-01292-3
Shejil Kumar, Jean Doyle, Cameron Wood, Roxana Heriseanu, Gerard Weber, Lianne Nier, James W Middleton, Lyn March, Roderick J Clifton-Bligh, Christian M Girgis
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引用次数: 0

摘要

在创伤性脊髓损伤(TSCI)后的最初 2-3 年中,骨质加速流失很常见,尤其是在股骨远端和胫骨近端。很少有研究探讨抗骨质吸收剂对预防创伤性脊髓损伤后急性骨质流失的疗效,有关膝关节骨矿物质密度(BMD)或两年后随访的数据也很有限。2018 年至 2023 年期间,悉尼皇家北岸医院和皇家康复中心开展了一项开放标签非随机研究。患有TSCI(病程≤12周)的 "急性介入队列"(n = 11)在基线时接受了4毫克唑来膦酸(ZOL)的单次输注。患有TSCI(病程1-5年)的 "慢性非干预队列"(n = 9)不接受唑来膦酸治疗。所有参与者都接受了基线和6个月一次的血液检测(包括CTx和P1NP)以及12个月一次的DXA BMD扫描(包括股骨远端和胫骨近端)。参与者主要为白种人,男性(平均年龄 38.4 岁)。基线时,"急性 "组群的血清 CTx、P1NP 和硬骨蛋白浓度较高,而 "慢性 "组群的左髋和膝关节 BMD 较低。大多数急性 TSCI 患者在服用 ZOL 后出现急性期反应(9/11;82%)。在急性组群中,左髋部 BMD 在 48 个月内平均下降了约 15%。左股骨远端和胫骨近端 BMD 在 12 个月时平均下降约 6-13%,在 48 个月时下降约 20-23%,运动完全型 TSCI 患者的 BMD 有更大的下降趋势。在急性 TSCI 中输注一次早期 ZOL 无法缓解髋关节和膝关节 BMD 的快速下降。需要进行前瞻性对照研究,以确定预防急性 TSCI 后早期骨质流失的最佳策略。
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Preventing OsteoPorosis in Spinal Cord Injury (POPSCI) Study-Early Zoledronic Acid Infusion in Patients with Acute Spinal Cord Injury.

Accelerated sub-lesional bone loss is common in the first 2-3 years after traumatic spinal cord injury (TSCI), particularly in the distal femur and proximal tibia. Few studies have explored efficacy of antiresorptives for acute bone loss prevention post-TSCI, with limited data for knee bone mineral density (BMD) or beyond two years follow-up. An open-label non-randomized study was performed at Royal North Shore Hospital and Royal Rehab Centre, Sydney between 2018 and 2023. An 'acute interventional cohort' (n = 11) with TSCI (duration ≤ 12-weeks) received a single infusion of 4 mg zoledronic acid (ZOL) at baseline. A 'chronic non-interventional cohort' (n = 9) with TSCI (duration 1-5-years) did not receive ZOL. All participants underwent baseline and 6-monthly blood tests (including CTx and P1NP) and 12-monthly DXA BMD scans (including distal femur and proximal tibia). Participants were predominantly Caucasian and male (mean age 38.4 years). At baseline, the 'acute' cohort had higher serum CTx, P1NP and sclerostin concentrations, while the 'chronic' cohort had lower left hip and knee BMD. Majority with acute TSCI experienced an acute phase reaction after ZOL (9/11; 82%). In the acute cohort, left hip BMD fell by mean ~ 15% by 48 months. Left distal femoral and proximal tibial BMD declined by mean ~ 6-13% at 12 months and ~ 20-23% at 48 months, with a tendency towards greater BMD loss in motor-complete TSCI. A single early ZOL infusion in acute TSCI could not attenuate rapidly declining hip and knee BMD. Prospective controlled studies are required to establish the optimal strategy for preventing early bone loss after acute TSCI.

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