Department of Craniomaxillofacial Regenerative Medicine, Dental and Trauma Research Detachment, Fort Sam Houston, Texas, 78234.
Department of Biomedical Engineering, University of Texas at San Antonio, San Antonio, Texas, 78249.
J Biomed Mater Res B Appl Biomater. 2019 Jul;107(5):1491-1503. doi: 10.1002/jbm.b.34241. Epub 2018 Sep 28.
At least 26% of recent battlefield injuries are to the craniomaxillofacial (CMF) region. Recombinant human bone morphogenetic protein 2 (rhBMP-2) is used to treat CMF open fractures, but several complications have been associated with its use. This study tested the efficacy and safety of a lower (30% recommended) dose of rhBMP-2 to treat mandibular fractures. rhBMP-2 delivered via a polyurethane (PUR) and hydroxyapatite/β-tricalcium phosphate (Mastergraft®) scaffold was evaluated in a 2 cm segmental mandibular defect in minipigs. Bone regeneration was analyzed at 4, 8, and 12 weeks postsurgery using clinical computed tomography (CT) and rhBMP-2, and inflammatory marker concentrations were analyzed in serum and surgery-site drain effluent. CT scans revealed that pigs treated with PUR-Mastergraft® + rhBMP-2 had complete bone bridging, while the negative control group showed incomplete bone-bridging (n = 6). Volumetric analysis of regenerated bone showed that the PUR-Mastergraft® + rhBMP-2 treatment generated significantly more bone than control by 4 weeks, a trend that continued through 12 weeks. Variations in inflammatory analytes were detected in drain effluent samples and saliva but not in serum, suggesting a localized healing response. Importantly, the rhBMP-2 group did not exhibit an excessive increase in inflammatory analytes compared to control. Treatment with low-dose rhBMP-2 increases bone regeneration capacity in pigs with mandibular continuity defects and restores bone quality. Negative complications from rhBMP-2, such as excessive inflammatory analyte levels, were not observed. Together, these results suggest that treatment with low-dose rhBMP-2 is efficacious and may improve safety when treating CMF open fractures. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 107B: 1491-1503, 2019.
最近战场上至少有 26%的创伤发生在颅面区域。重组人骨形态发生蛋白 2(rhBMP-2)用于治疗颅面开放性骨折,但与使用 rhBMP-2 相关的几种并发症已经被报道。本研究测试了较低(推荐剂量的 30%)剂量的 rhBMP-2 治疗下颌骨骨折的疗效和安全性。rhBMP-2 通过聚氨酯(PUR)和羟基磷灰石/β-磷酸三钙(Mastergraft®)支架递送至小型猪的 2cm 节段性下颌骨缺损中。术后 4、8 和 12 周时,使用临床计算机断层扫描(CT)和 rhBMP-2 分析骨再生情况,并分析血清和手术部位引流液中的炎症标志物浓度。CT 扫描显示,用 PUR-Mastergraft®+rhBMP-2 治疗的猪完全桥接了骨骼,而阴性对照组显示不完全桥接(n=6)。再生骨的体积分析表明,PUR-Mastergraft®+rhBMP-2 治疗在 4 周时比对照组产生了显著更多的骨,这种趋势一直持续到 12 周。引流液样本和唾液中的炎症分析物存在变化,但血清中没有,表明存在局部愈合反应。重要的是,rhBMP-2 组与对照组相比,炎症分析物没有过度增加。用低剂量 rhBMP-2 治疗可增加小型猪下颌骨连续性缺损的骨再生能力,并恢复骨质量。未观察到 rhBMP-2 的负面并发症,如炎症分析物水平过高。这些结果表明,用低剂量 rhBMP-2 治疗在治疗颅面开放性骨折时是有效的,并且可能提高安全性。2018 年 Wiley 期刊公司。J 生物医学材料研究杂志 B 部分:应用生物材料 107B:1491-1503,2019 年。