Wikesjö Ulf M E, Qahash Mohammed, Polimeni Giuseppe, Susin Cristiano, Shanaman Richard H, Rohrer Michael D, Wozney John M, Hall Jan
Laboratory for Applied Periodontal and Craniofacial Regeneration, Medical College of Georgia, School of Dentistry, Augusta, GA 30912, USA.
J Clin Periodontol. 2008 Nov;35(11):1001-10. doi: 10.1111/j.1600-051X.2008.01321.x.
Studies using ectopic rodent, orthotopic canine, and non-human primate models show that bone morphogenetic proteins (BMPs) coated onto titanium surfaces induce local bone formation. The objective of this study was to examine the ability of recombinant human BMP-2 (rhBMP-2) coated onto a titanium porous oxide implant surface to stimulate local bone formation including osseointegration and vertical augmentation of the alveolar ridge.
Bilateral, critical-size, 5 mm, supra-alveolar, peri-implant defects were created in 12 young adult Hound Labrador mongrel dogs. Six animals received implants coated with rhBMP-2 at 0.75 or 1.5 mg/ml, and six animals received implants coated with rhBMP-2 at 3.0 mg/ml or uncoated control. Treatments were randomized between jaw quadrants. The mucoperiosteal flaps were advanced, adapted and sutured to submerge the implants for primary intention healing. The animals received fluorescent bone markers at weeks 3, 4, 7 and 8 post-surgery when they were euthanized for histologic evaluation.
Jaw quadrants receiving implants coated with rhBMP-2 exhibited gradually regressing swelling that became hard to palpate disguising the contours of the implants. The histologic evaluation showed robust bone formation reaching or exceeding the implant platform. The newly formed bone exhibited characteristics of the adjoining resident Type II bone including cortex formation for sites receiving implants coated with rhBMP-2 at 0.75 or 1.5 mg/ml. Sites receiving implants coated with rhBMP-2 at 3.0 mg/ml exhibited more immature trabecular bone formation, seroma formation and peri-implant bone remodelling resulting in undesirable implant displacement. Control implants exhibited minimal, if any, bone formation. Thus, implants coated with rhBMP-2 at 0.75, 1.5 and 3.0 mg/ml exhibited significant bone formation (height and area) compared with the sham-surgery control averaging (+/-SD) 4.4+/-0.4, 4.2+/-0.7 and 4.2+/-1.2 versus 0.8+/-0.3 mm; and 5.0+/-2.2, 5.6+/-2.2 and 7.4+/-3.5 versus 0.7+/-0.3 mm(2), respectively (p<0.01). All the treatment groups exhibited clinically relevant osseointegration.
rhBMP-2 coated onto titanium porous oxide implant surfaces induced clinically relevant local bone formation including vertical augmentation of the alveolar ridge and osseointegration. Higher concentrations/doses were associated with untoward effects.
使用异位啮齿动物、原位犬类和非人类灵长类动物模型的研究表明,涂覆在钛表面的骨形态发生蛋白(BMPs)可诱导局部骨形成。本研究的目的是检查涂覆在钛多孔氧化物植入物表面的重组人BMP-2(rhBMP-2)刺激局部骨形成的能力,包括骨整合和牙槽嵴垂直增高。
在12只年轻成年杂交寻血猎犬中制造双侧、临界尺寸、5mm、牙槽上、种植体周围缺损。6只动物接受涂有0.75或1.5mg/ml rhBMP-2的植入物,6只动物接受涂有3.0mg/ml rhBMP-2或未涂覆的对照植入物。治疗在颌象限之间随机分配。推进、贴合并缝合粘骨膜瓣以将植入物浸没以实现一期愈合。在术后第3、4、7和8周对动物给予荧光骨标记物,然后对其实施安乐死以进行组织学评估。
接受涂有rhBMP-2植入物的颌象限肿胀逐渐消退,变得难以触及,掩盖了植入物的轮廓。组织学评估显示有强劲的骨形成,达到或超过植入物平台。新形成的骨表现出相邻固有II型骨的特征,包括接受涂有0.75或1.5mg/ml rhBMP-2植入物部位的皮质形成。接受涂有3.0mg/ml rhBMP-2植入物的部位表现出更多不成熟的小梁骨形成、血清肿形成和种植体周围骨重塑,导致植入物出现不良移位。对照植入物显示出极少的骨形成(如果有的话)。因此,与假手术对照组相比,涂有0.75、1.5和3.0mg/ml rhBMP-2的植入物显示出显著的骨形成(高度和面积),平均(±标准差)分别为4.4±0.4、4.2±0.7和4.2±1.2对0.8±0.3mm;以及5.0±2.2、5.6±2.2和7.4±3.5对0.7±0.3mm²(p<0.01)。所有治疗组均表现出临床相关的骨整合。
涂覆在钛多孔氧化物植入物表面的rhBMP-2可诱导临床相关的局部骨形成,包括牙槽嵴垂直增高和骨整合。较高浓度/剂量与不良影响相关。