Division of Orthopaedic Surgery, Shriners Hospital for Children, Montreal Children Hospital, McGill University , Montreal, QC , Canada ; Department of Orthopaedic Surgery, University of Dammam , Dammam , Saudi Arabia.
Division of Orthopaedic Surgery, Shriners Hospital for Children, Montreal Children Hospital, McGill University , Montreal, QC , Canada ; Department of Orthopaedic Surgery, King Abdulaziz University , Jeddah , Saudi Arabia.
Front Endocrinol (Lausanne). 2014 Dec 10;5:214. doi: 10.3389/fendo.2014.00214. eCollection 2014.
Distraction osteogenesis (DO) is a surgical technique where gradual and controlled separation of two bony fragments following an osteotomy leads to the induction of new bone formation in the distracted gap. DO is used for limb lengthening, correction of bony deformities, and the replacement of bone loss secondary to infection, trauma, and tumors. Although DO gives satisfactory results in most cases, one major drawback of this technique is the prolonged period of time the external fixator has to be kept on until the newly formed bone consolidates thus leading to numerous complications. Numerous attempts at accelerating bone formation during DO have been reported. One specific approach is manipulation of the mechanical environment during DO by applying changes in the standard protocol of distraction. Attempts at changing this mechanical environment led to mixed results. Increasing the rate or applying acute distraction, led to poor bone formation in the distracted zone. On the other hand, the addition of compressive forces (such as weight bearing, alternating distraction with compression or by over-lengthening, and then shortening) has been reported to increase bone formation. It still remains unclear why these alterations may lead to changes in bone formation. While the cellular and molecular changes occurring during the standard DO protocol, specifically increased expression of transforming growth factor-β1, platelet-derived growth factor, insulin-like growth factor, basic fibroblast growth factor, vascular endothelial growth factor, and bone morphogenic proteins have been extensively investigated, the literature is sparse on the changes occurring when this protocol is altered. It is the purpose of this article to review the pertinent literature on the changes in the expression of various proteins and molecules as a result of changes in the mechanical loading technique in DO and try to define potential future research directions.
骨牵引成骨术(DO)是一种外科技术,通过对骨切开术后的两块骨碎片进行逐渐和受控的分离,导致在牵引间隙中诱导新骨形成。DO 用于肢体延长、矫正骨畸形以及感染、创伤和肿瘤引起的骨丢失的替代。尽管在大多数情况下 DO 都能取得满意的效果,但该技术的一个主要缺点是外部固定器必须保持很长时间,直到新形成的骨巩固,从而导致许多并发症。已经有许多尝试在 DO 期间加速骨形成的报道。一种特定的方法是通过改变 DO 的标准方案来操纵机械环境。尝试改变这种机械环境导致了混合结果。增加速度或施加急性牵引会导致牵引区骨形成不良。另一方面,施加压缩力(例如负重、交替牵引与压缩或过度延长然后缩短)已被报道可增加骨形成。为什么这些改变可能导致骨形成的变化仍然不清楚。虽然在标准 DO 方案中发生的细胞和分子变化,特别是转化生长因子-β1、血小板衍生生长因子、胰岛素样生长因子、碱性成纤维细胞生长因子、血管内皮生长因子和骨形态发生蛋白的表达增加已经得到了广泛的研究,但关于改变方案时发生的变化的文献却很少。本文的目的是回顾关于在 DO 中改变机械加载技术时各种蛋白质和分子表达变化的相关文献,并尝试定义潜在的未来研究方向。