Quan Renfu, Ni Yueming, Zhang Liang, Xu Jinwei, Zheng Xuan, Yang Disheng
Department of Orthopedics, Xiaoshan Traditional Chinese Medical Hospital, Hangzhou 311200, ZhengJiang Province, China.
Department of Orthopedics, Xiaoshan Traditional Chinese Medical Hospital, Hangzhou 311200, ZhengJiang Province, China.
J Mech Behav Biomed Mater. 2014 Jul;35:102-10. doi: 10.1016/j.jmbbm.2014.03.007. Epub 2014 Apr 12.
Vertebroplasty using poly(methyl methacrylate) (PMMA) bone cement is the most common method to treat osteoporotic vertebral fractures. However, several questions of interest remain to be clarified, including how does PMMA affect the cement-bone interface area and surrounding bone tissue, can damaged bone tissues be repaired, how will PMMA change the bone interface over the long-term, and what happens to PMMA itself? The purpose of this study is to investigate these concerns and provide a basis for clinical evaluation. We made bone defects in the lumbar vertebrae of New Zealand rabbits as a model of osteoporosis and injected them with bone cement. A mechanical testing machine was used to perform axial compression, three-point bending, and twisting resistance tests to observe and investigate the short- and long-term biomechanical properties of PMMA after implantation. Optical, fluorescence, scanning electron microscopy, and nanoindentation were used to observe the changes in the interface microstructure. PMMA can rapidly establish the strong support with stable function in the near future. Biomechanical experiments showed that biomechanical property of bone cement group was significantly higher than those in the other two groups (P<0.05) biomechanical property of bone cement group may decline with the time, but it's still better than that of OP in the control group (P<0.05). Histomorphological observation result shows that under osteoporosis state the bone grows slower, also bone's rebuilding time extended. And in the later period, main bone's continuous osteoporosis has some impact on the interface. Nano-indentation testing shows that the young modulus and stiffness of the interface among bone, material and interface were significantly differences (P<0.05). Bone cement had gave the best nano indentation hardness, then was interface and bone tissue. PMMA bone cement was able to quickly support and stabilize the defect in the short term, and bone growth restarted at the bone interface and was tightly integrated. However, over the long-term, fluorescent signal was weakened, osteoclasts appeared, the mechanical indicators for both the interface and the whole vertebra decreased, and bone resorption was eventually greater than bone formation, resulting in bone loss. Therefore, vertebroplasty is not the end of treatment, and we need to further study ways to improve the bone cement material, which is crucial for long-term vertebroplasty efficacy, to better treat osteoporosis.
使用聚甲基丙烯酸甲酯(PMMA)骨水泥进行椎体成形术是治疗骨质疏松性椎体骨折最常用的方法。然而,仍有几个问题有待阐明,包括PMMA如何影响骨水泥-骨界面区域和周围骨组织、受损骨组织能否修复、PMMA长期如何改变骨界面以及PMMA本身会发生什么?本研究的目的是探讨这些问题,并为临床评估提供依据。我们在新西兰兔的腰椎制造骨缺损作为骨质疏松模型,并向其中注入骨水泥。使用机械试验机进行轴向压缩、三点弯曲和抗扭转试验,以观察和研究PMMA植入后的短期和长期生物力学性能。采用光学、荧光、扫描电子显微镜和纳米压痕法观察界面微观结构的变化。PMMA能够在短期内迅速建立起功能稳定的强力支撑。生物力学实验表明,骨水泥组的生物力学性能明显高于其他两组(P<0.05),骨水泥组的生物力学性能可能会随时间下降,但仍优于对照组中的骨质疏松组(P<0.05)。组织形态学观察结果表明,在骨质疏松状态下,骨生长较慢,骨重建时间也延长。并且在后期,主要骨的持续骨质疏松对界面有一定影响。纳米压痕测试表明,骨、材料和界面之间的界面杨氏模量和刚度存在显著差异(P<0.05)。骨水泥的纳米压痕硬度最佳,其次是界面和骨组织。PMMA骨水泥在短期内能够迅速支撑并稳定缺损部位,骨生长在骨界面重新开始并紧密融合。然而,从长期来看,荧光信号减弱,破骨细胞出现,界面和整个椎体的力学指标下降,最终骨吸收大于骨形成,导致骨质流失。因此,椎体成形术并非治疗的终点,我们需要进一步研究改进骨水泥材料的方法,这对于椎体成形术的长期疗效至关重要,以便更好地治疗骨质疏松症。