骨形态发生蛋白-2 存在时反向动化促进大鼠股骨大节段缺损的愈合。
Improved healing of large segmental defects in the rat femur by reverse dynamization in the presence of bone morphogenetic protein-2.
机构信息
Center for Advanced Orthopaedic Studies, Beth Israel Deaconess Medical Center, Harvard Medical School, 330, Brookline Avenue, RN-115, Boston, MA 02215, USA. V. Glatt:
出版信息
J Bone Joint Surg Am. 2012 Nov 21;94(22):2063-73. doi: 10.2106/JBJS.K.01604.
BACKGROUND
Large segmental defects in bone do not heal well and present clinical challenges. This study investigated modulation of the mechanical environment as a means of improving bone healing in the presence of bone morphogenetic protein (BMP)-2. Although the influence of mechanical forces on the healing of fractures is well established, no previous studies, to our knowledge, have described their influence on the healing of large segmental defects. We hypothesized that bone-healing would be improved by initial, low-stiffness fixation of the defect, followed by high-stiffness fixation during the healing process. We call this reverse dynamization.
METHODS
A rat model of a critical-sized femoral defect was used. External fixators were constructed to provide different degrees of stiffness and, importantly, the ability to change stiffness during the healing process in vivo. Healing of the critical-sized defects was initiated by the implantation of 11 μg of recombinant human BMP (rhBMP)-2 on a collagen sponge. Groups of rats receiving BMP-2 were allowed to heal with low, medium, and high-stiffness fixators, as well as under conditions of reverse dynamization, in which the stiffness was changed from low to high at two weeks. Healing was assessed at eight weeks with use of radiographs, histological analysis, microcomputed tomography, dual x-ray absorptiometry, and mechanical testing.
RESULTS
Under constant stiffness, the low-stiffness fixator produced the best healing after eight weeks. However, reverse dynamization provided considerable improvement, resulting in a marked acceleration of the healing process by all of the criteria of this study. The histological data suggest that this was the result of intramembranous, rather than endochondral, ossification.
CONCLUSIONS
Reverse dynamization accelerated healing in the presence of BMP-2 in the rat femur and is worthy of further investigation as a means of improving the healing of large segmental bone defects.
CLINICAL RELEVANCE
These data provide the basis of a novel, simple, and inexpensive way to improve the healing of critical-sized defects in long bones. Reverse dynamization may also be applicable to other circumstances in which bone-healing is problematic.
背景
大段骨缺损不易愈合,存在临床挑战。本研究探讨了调节力学环境作为改善骨形态发生蛋白(BMP)-2 存在下骨愈合的一种方法。尽管机械力对骨折愈合的影响已得到充分证实,但据我们所知,以前没有研究描述过它们对大段骨缺损愈合的影响。我们假设,通过最初的低刚度固定缺陷,然后在愈合过程中采用高刚度固定,可以改善骨愈合。我们称之为反向动化。
方法
采用大鼠股骨临界尺寸缺损模型。构建外固定器以提供不同程度的刚度,重要的是,能够在体内愈合过程中改变刚度。通过在胶原蛋白海绵上植入 11μg 重组人 BMP(rhBMP)-2 来启动临界尺寸缺损的愈合。接受 BMP-2 治疗的大鼠组分别采用低、中、高刚度固定器以及反向动化固定器进行愈合,其中在两周时刚度从低变为高。在 8 周时,通过 X 线片、组织学分析、微计算机断层扫描、双 X 射线吸收测定法和力学测试评估愈合情况。
结果
在刚度恒定的情况下,低刚度固定器在 8 周后产生了最佳的愈合效果。然而,反向动化提供了相当大的改善,通过本研究的所有标准都显著加速了愈合过程。组织学数据表明,这是膜内而不是软骨内成骨的结果。
结论
反向动化加速了大鼠股骨中 BMP-2 存在下的愈合,值得进一步研究,作为改善长骨大段骨缺损愈合的一种方法。
临床意义
这些数据为一种新颖、简单且经济的方法提供了基础,可改善长骨临界尺寸缺损的愈合。反向动化也可能适用于其他存在骨愈合问题的情况。