摘要
最小化的概念被定义为一种局灶性骨形成,其特征是破骨细胞之前没有骨吸收。在极小化、成骨和成骨过程中自闭症活动是解耦的。可以发现旧骨与新骨之间的线性边界。Frost等人推测,小梁的最小化可以在整个生命中持续下去。迷你概念建模并不是什么新鲜事,但是它的功能和本质还没有完全被理解。我们将从以下五个方面对基于最小化的地层进行综述:1.将最小化与远程化进行比较。灵对10项;2.描述组织学观察,以表征重塑和最小形成部位;3.提供骨合成剂的证据,这些药物可启动骨极小化4.探讨骨微区形成的机制和靶细胞;5.解释骨形成过程中成骨潜能和小梁连通性的增加;描绘m骨质疏松症中骨种植界面和种植体周围成骨的模式。这篇综述提供了一个关于最小化的全面和潜在的深入的知识。骨内平衡的研究及在提高骨质疏松牙种植成功率方面的应用前景。
关键词: 迷你模型,重塑,骨质疏松,种植,骨整合,eldecalcitol。
Current Molecular Medicine
Title:Bone Minimodeling, a Special Modeling Pattern and Potential as Therapeutic Target for Osteoporosis
Volume: 18 Issue: 4
关键词: 迷你模型,重塑,骨质疏松,种植,骨整合,eldecalcitol。
摘要: The concept of minimodeling is defined as a kind of focal bone formation that features the absence of preceding bone absorption by osteoclasts. In the process of minimodeling, osteogenetic and osteoclastic activities are decoupled. Linear boundary between old bone and new bone can be discovered. Frost et al. presumed that minimodeling in trabeculae can continue throughout life. The concept of minimodeling is not new, however its function and nature are still imperfectly understood. Our review will focus on minimodeling-based formation in 5 aspects below: 1. compare the minimodeling with remodeling regarding 10 items; 2. describe the histological observation to characterize remodeling and minimodeling formation sites; 3. present evidence of bone anabolic agents which start bone minimodeling; 4. discuss the mechanism and target cells involved in bone minimodeling; 5. interpretate the increased osteogenic potential and trabecular connectivity with minimodeling-based formation; 6. Depict modeling patterns of the bone implant interface and peri-implant osteogenesis in osteoporosis. This review provides an in-depth knowledge regarding minimodeling comprehensively and its potential contributions in skeletal homeostasis and application prospect in improving the success rate of dental implant in osteoporosis.
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Cite this article as:
Bone Minimodeling, a Special Modeling Pattern and Potential as Therapeutic Target for Osteoporosis, Current Molecular Medicine 2018; 18 (4) . https://dx.doi.org/10.2174/1566524018666181004113128
DOI https://dx.doi.org/10.2174/1566524018666181004113128 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
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