Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY, United States of America.
Department of Orthopaedics Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
PLoS One. 2017 Oct 11;12(10):e0185446. doi: 10.1371/journal.pone.0185446. eCollection 2017.
Small animal studies have demonstrated significant high-dose recombinant parathyroid hormone1-34 (rPTH1-34) effects on intercalary allograft healing. Towards a human adjuvant therapy to decrease non-unions, we evaluated rPTH1-34 safety and efficacy in a clinically relevant canine femoral allograft model. Adult female mongrel hounds (n = 20) received a 5cm mid-diaphyseal osteotomy reconstructed with a plated allograft, and were randomized to: 1) Placebo (n = 5; daily saline), 2) Continuous rPTH1-34 (n = 7; 5 μg/kg/day s.c. from day 1-55 post-op), or 3) Delayed rPTH1-34 (n = 8; 5 μg/kg/day s.c. from day 14-28 post-op). Safety was assessed by physical behavior and blood calcium monitoring. Cone beam CT (CB-CT) was performed on days 14, 28 and 56 post-op to assess 2D cortical healing, 3D bone volume, and Union Ratio. Biomechanical testing and dynamic histomorphometry were also performed. The high drug dose was poorly tolerated, as most dogs receiving rPTH1-34 had to be given intravenous saline, and one dog died from hypercalcemia. Continuous rPTH1-34 significantly increased 2D healing and callus volumes at 4-weeks versus Placebo, and sustained the significant increase in cortical union at 8-week (p<0.05). These rPTH1-34 effects were confirmed by histomorphometry, revealing significant increases in mineral apposition rates (MAR) on host bone and graft-host junctions (p<0.05). Delayed rPTH1-34 significantly increased callus volume and MAR at 8 weeks (p<0.05). Although no biomechanical differences were observed, as expected for early healing, the results demonstrated that 2D RUST scoring significantly correlated with torsional biomechanics (p<0.01). In conclusion, 8-weeks of intermittent high-dose rPTH1-34 treatment significantly increases callus formation and accelerates bony union of intercalary massive allografts in a clinically relevant canine model, but with serious side-effects from hypercalcemia.
小动物研究表明,大剂量重组甲状旁腺素 1-34(rPTH1-34) 对中间段同种异体移植物愈合有显著影响。为了寻找一种减少骨不连的人类佐剂疗法,我们在临床相关的犬股骨同种异体移植模型中评估了 rPTH1-34 的安全性和疗效。成年雌性杂种犬( n = 20)接受 5cm 中段骨干切开复位,用钢板重建同种异体移植,随机分为:1) 安慰剂组( n = 5; 术后第 1-55 天每天给予生理盐水),2) 连续 rPTH1-34 组( n = 7; 术后第 1-55 天每天皮下给予 5μg/kg),或 3) 延迟 rPTH1-34 组( n = 8; 术后第 14-28 天每天皮下给予 5μg/kg)。通过身体行为和血钙监测评估安全性。术后第 14、28 和 56 天进行锥形束 CT(CB-CT)检查,评估二维皮质愈合、三维骨体积和愈合率。还进行了生物力学测试和动态组织形态测量。高药物剂量耐受性差,因为大多数接受 rPTH1-34 治疗的狗不得不给予静脉生理盐水,一只狗死于高钙血症。连续 rPTH1-34 治疗在 4 周时显著增加了 2 维愈合和骨痂体积,与安慰剂相比,8 周时皮质愈合的显著增加持续存在(p<0.05)。组织形态计量学证实了 rPTH1-34 的这些作用,显示宿主骨和移植物-宿主交界处的矿化沉积率(MAR)显著增加(p<0.05)。延迟 rPTH1-34 治疗在 8 周时显著增加了骨痂体积和 MAR(p<0.05)。尽管由于早期愈合,预计不会有生物力学差异,但结果表明,2 维 RUST 评分与扭转生物力学显著相关(p<0.01)。总之,8 周的间歇性高剂量 rPTH1-34 治疗显著增加了中间段同种异体大块移植物的骨痂形成和加速了骨愈合,但伴有严重的高钙血症副作用。