Müller Ralph
Institute for Biomedical Engineering, Swiss Federal Institute of Technology (ETH) and University of Zürich.
Osteoporos Int. 2005 Mar;16 Suppl 2:S25-35. doi: 10.1007/s00198-004-1701-7. Epub 2004 Aug 31.
The mechanical behavior of trabecular bone depends on the internal bone structure. It is generally accepted now that the trabecular bone structure is a result of a load adaptive bone remodeling. The mathematical laws that relate bone remodeling to the local state of stress and strain, however, are still under investigation. The aim of this project was to investigate if changes in the trabecular architecture as observed with age-related bone loss and osteoporosis can be predicted from a computer model that simulates bone resorption after hormone depletion based on realistic models of trabecular microstructure using micro-computed tomography (muCT). A compact desktop muCT providing a nominal isotropic resolution of 14 mum was used to measure two groups of seven trabecular bone specimens from pre-menopausal and post-menopausal women respectively. A novel algorithm was developed to simulate age-related bone loss for the specimens in the first group. The algorithm, also referred to as simulated bone atrophy (SIBA), describes a truly three-dimensional approach and is based directly on cellular bone remodeling with an underlying realistic time frame. Bone resorption is controlled by osteoclastic penetration depth and bone formation is governed by the efficiency level of the osteoblasts. The simulation itself describes an iterative process with a cellular remodeling cycle of 197 days. Activation frequency is controllable and can be adjusted for the different phases of pre-, peri- and post-menopause. For our simulations, osteoblastic and osteoclastic activities were in balance until the onset of menopause, set to be at the age of 50 years. In that period, the structure remained almost constant. After the onset of menopause an imbalance in the cell activities was modeled resulting in a net bone loss. The doubling of the activation frequency in the peri-menopausal phase caused a pronounced loss. Using advanced animation tools and quantitative bone morphometry, the changes in bone architecture associated with the bone loss were monitored over an average observation time of 43 years until the age of 80 years. In that time, bone volume density decreased monotonously with the progression of the simulation for all specimens. Right after the onset of menopause, bone was lost fast, where with the progression of age losses slowed down. The structures at the end-point of the simulations were then compared qualitatively and quantitatively to the structures of the post-menopausal group with all morphometric indices being within a narrow margin of error. These results suggest the feasibility of transforming "normal" to "osteopenic" bone on a microstructural level yielding in realistic bone models similar in appearance as well as in structural behavior if compared to a post-menopausal group of women.
松质骨的力学行为取决于其内部结构。现在人们普遍认为,松质骨结构是负载适应性骨重塑的结果。然而,将骨重塑与局部应力和应变状态联系起来的数学定律仍在研究之中。本项目的目的是研究能否通过一个计算机模型预测与年龄相关的骨质流失和骨质疏松症中观察到的松质骨结构变化。该计算机模型基于使用微型计算机断层扫描(μCT)的真实松质骨微观结构模型,模拟激素缺乏后的骨吸收。使用一台标称各向同性分辨率为14μm的紧凑型台式μCT分别测量两组来自绝经前和绝经后女性的七块松质骨标本。开发了一种新算法来模拟第一组标本中与年龄相关的骨质流失。该算法,也称为模拟骨萎缩(SIBA),描述了一种真正的三维方法,直接基于具有潜在真实时间框架的细胞骨重塑。骨吸收由破骨细胞穿透深度控制,骨形成由成骨细胞的效率水平控制。模拟本身描述了一个迭代过程,细胞重塑周期为197天。激活频率是可控的,可以针对绝经前、围绝经期和绝经后的不同阶段进行调整。在我们的模拟中,直到绝经开始(设定为50岁),成骨细胞和破骨细胞的活动保持平衡。在此期间,结构几乎保持不变。绝经开始后,模拟细胞活动的不平衡导致净骨质流失。围绝经期激活频率加倍导致明显的骨质流失。使用先进的动画工具和定量骨形态计量学,在平均43年的观察期内监测与骨质流失相关的骨结构变化,直至80岁。在这段时间里,所有标本的骨体积密度随着模拟的进行单调下降。绝经刚开始时,骨质快速流失,随着年龄增长,流失速度减缓。然后将模拟终点的结构与绝经后组的结构进行定性和定量比较,所有形态计量指标的误差范围都很窄。这些结果表明,在微观结构水平上,将“正常”骨转化为“骨质减少”骨是可行的,与绝经后女性组相比,生成的真实骨模型在外观和结构行为上都很相似。