Institute for Biomechanics, ETH Zurich, Wolfgang-Pauli-Strasse 10, 8093 Zurich, Switzerland.
Bone. 2013 Jan;52(1):485-92. doi: 10.1016/j.bone.2012.09.008. Epub 2012 Sep 14.
Computational models are an invaluable tool to test different mechanobiological theories and, if validated properly, for predicting changes in individuals over time. Concise validation of in silico models, however, has been a bottleneck in the past due to a lack of appropriate reference data. Here, we present a strain-adaptive in silico algorithm which is validated by means of experimental in vivo loading data as well as by an in vivo ovariectomy experiment in the mouse. The maximum prediction error following four weeks of loading resulted in 2.4% in bone volume fraction (BV/TV) and 8.4% in other bone structural parameters. Bone formation and resorption rate did not differ significantly between experiment and simulation. The spatial distribution of formation and resorption sites matched in 55.4% of the surface voxels. Bone loss was simulated with a maximum prediction error of 12.1% in BV/TV and other bone morphometric indices, including a saturation level after a few weeks. Dynamic rates were more difficult to be accurately predicted, showing evidence for significant differences between simulation and experiment (p<0.05). The spatial agreement still amounted to 47.6%. In conclusion, we propose a computational model which was validated by means of experimental in vivo data. The predictive value of an in silico model may become of major importance if the computational model should be applied in clinical settings to predict bone changes due to disease and test the efficacy of potential pharmacological interventions.
计算模型是测试不同机械生物学理论的宝贵工具,如果经过适当验证,还可以预测个体随时间的变化。然而,由于缺乏适当的参考数据,过去简明验证计算模型一直是一个瓶颈。在这里,我们提出了一种应变自适应的计算算法,该算法通过实验体内加载数据以及在小鼠体内去卵巢实验进行了验证。经过四周的加载后,最大预测误差导致骨体积分数(BV/TV)的变化为 2.4%,其他骨结构参数的变化为 8.4%。实验和模拟之间的骨形成和吸收速率没有显著差异。形成和吸收部位的空间分布在 55.4%的表面体素中匹配。骨丢失用最大预测误差为 12.1%的 BV/TV 和其他骨形态计量学指标进行模拟,包括几周后达到饱和水平。动态速率更难准确预测,表明模拟与实验之间存在显著差异(p<0.05)。空间一致性仍然达到 47.6%。总之,我们提出了一种计算模型,该模型通过实验体内数据进行了验证。如果计算模型应在临床环境中应用于预测疾病引起的骨变化并测试潜在药物干预的效果,则其预测价值可能变得非常重要。