Latimer Jessica, Yilmaz Birtan, Feher Balazs, Shiba Takahiko, Fretwurst Tobias, Mitlak Bruce, Lanske Beate, Kostenuik Paul, Giannobile William V
Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, Massachusetts, USA.
Department of Oral Biology, University Clinic of Dentistry, Medical University of Vienna, Vienna, Austria.
Clin Oral Implants Res. 2025 Apr;36(4):471-480. doi: 10.1111/clr.14397. Epub 2025 Jan 9.
Abaloparatide (ABL) is a synthetic parathyroid hormone-related protein analog developed as an anabolic drug to treat osteoporosis. ABL increases bone mineral density (BMD) of the long bones and spine; however, the influence of ABL on alveolar bone regeneration remains unknown. This study assessed the effects of systemic ABL administration on tooth extraction socket healing and dental implant osseointegration in a preclinical rodent model.
Sprague-Dawley rats received daily subcutaneous injection of ABL (25 μg/kg) or vehicle (VEH) at the time of maxillary first molar (M1) extraction surgery; animals underwent either: (1) unilateral M1 extraction followed by sacrifice at 10 or 42d or (2) bilateral M1 extraction followed by staged implant placement in osteotomies with standardized defects and sacrifice at 21 or 28d.
Micro-computed tomography (micro-CT) analysis demonstrated that ABL increased bone volume fraction (p = 0.004) and bone mineral density (BMD) (p = 0.006) of regenerated extraction sockets at 42d. Micro-CT of the femur validated systemic effects of ABL, showing greater trabecular BMD after 6 (p < 0.01), 9 (p < 0.001), and 14 (p < 0.001) weeks of treatment. Histomorphometry confirmed a higher mineralized bone area with ABL treatment in extraction sockets at 42d (p = 0.03) and in the regenerated peri-implant bone at 21d post-implant placement (p = 0.01) compared to control.
Systemic ABL administration enhances osteogenesis in extraction sockets prior to implant placement and accelerates peri-implant bone formation in the early phase of healing in the present rodent model.
阿巴洛肽(ABL)是一种合成的甲状旁腺激素相关蛋白类似物,作为一种合成代谢药物用于治疗骨质疏松症。ABL可增加长骨和脊柱的骨矿物质密度(BMD);然而,ABL对牙槽骨再生的影响尚不清楚。本研究在临床前啮齿动物模型中评估了全身给予ABL对拔牙窝愈合和牙种植体骨整合的影响。
在拔除上颌第一磨牙(M1)手术时,将斯普拉格-道利大鼠每日皮下注射ABL(25μg/kg)或赋形剂(VEH);动物进行以下操作之一:(1)单侧M1拔除,然后在10天或42天时处死;或(2)双侧M1拔除,然后在标准化骨缺损的截骨术中分阶段植入种植体,并在21天或28天时处死。
显微计算机断层扫描(micro-CT)分析表明,ABL可增加42天时再生拔牙窝的骨体积分数(p = 0.004)和骨矿物质密度(BMD)(p = 0.006)。股骨的micro-CT验证了ABL的全身效应,显示治疗6周(p < 0.01)、9周(p < 0.001)和14周(p < 0.001)后小梁BMD更高。组织形态计量学证实,与对照组相比,ABL治疗在42天时拔牙窝(p = 0.03)和种植体植入后21天时再生的种植体周围骨(p = 0.01)中矿化骨面积更高。
在本啮齿动物模型中,全身给予ABL可增强种植体植入前拔牙窝的成骨作用,并在愈合早期加速种植体周围骨形成。