Institute for Modelling and Simulation of Biomechanical Systems, University of Stuttgart, Stuttgart, Germany; Stuttgart Center for Simulation Science (SC SimTech), Stuttgart, Germany. Electronic address: http://bit.ly/2Tqx_PA.
Institute for Modelling and Simulation of Biomechanical Systems, University of Stuttgart, Stuttgart, Germany; Stuttgart Center for Simulation Science (SC SimTech), Stuttgart, Germany.
Acta Biomater. 2020 Apr 1;106:193-207. doi: 10.1016/j.actbio.2020.02.007. Epub 2020 Feb 11.
Throughout the process of aging, dynamic changes of bone material, micro- and macro-architecture result in a loss of strength and therefore in an increased likelihood of fragility fractures. To date, precise contributions of age-related changes in bone (re)modeling and (de)mineralization dynamics to this fragility increase are not completely understood. Here, we present an image-based deep learning approach to quantitatively describe the effects of short-term aging and adaptive response to cyclic loading applied to proximal mouse tibiae and fibulae. Our approach allowed us to perform an end-to-end age prediction based on μCT imaging to determine the dynamic biological process of aging during a two week period, therefore permitting short-term bone aging analysis with 95% accuracy in predicting time points. In a second application, our deep learning analysis reveals that two weeks of in vivo mechanical loading are associated with an underlying rejuvenating effect of 5 days. Additionally, by quantitatively analyzing the learning process, we could, for the first time, identify the localization of the age-relevant encoded information and demonstrate 89% load-induced similarity of these locations in the loaded tibia with younger control bones. These data therefore suggest that our method enables identifying a general prognostic phenotype of a certain skeletal age as well as a temporal and localized loading-treatment effect on this apparent skeletal age for the studied mouse tibia and fibula. Future translational applications of this method may provide an improved decision-support method for osteoporosis treatment at relatively low cost. STATEMENT OF SIGNIFICANCE: Bone is a highly complex and dynamic structure that undergoes changes during the course of aging as well as in response to external stimuli, such as loading. Automatic assessment of "age" and "state" of the bone may lead to early prognosis of deceases such as osteoporosis and enables evaluating the effects of certain treatments. Here, we present an artificial intelligence-based method capable of automatically predicting the skeletal age from μCT images with 95% accuracy. Additionally, we utilize it to demonstrate the rejuvenation effects of in-vivo loading treatment on bones. We further, for the first time, break down aging-related local changes in bone by quantitatively analyzing "what the age assessment model has learned" and use this information to investigate the structural details of rejuvenation process.
在整个衰老过程中,骨的物质、微观和宏观结构的动态变化导致强度丧失,从而增加了脆性骨折的可能性。迄今为止,年龄相关的骨(再)建模和(去)矿化动力学变化对这种脆弱性增加的确切贡献尚不完全清楚。在这里,我们提出了一种基于图像的深度学习方法,定量描述短期衰老和对应用于近侧小鼠胫骨和腓骨的循环加载的适应性反应对脆性增加的影响。我们的方法允许我们基于 μCT 成像进行端到端的年龄预测,以确定两周内衰老的动态生物学过程,从而以 95%的准确度进行短期骨龄分析,预测时间点。在第二个应用中,我们的深度学习分析表明,两周的体内机械加载与 5 天的潜在再生作用有关。此外,通过对学习过程进行定量分析,我们首次能够确定与年龄相关的编码信息的定位,并证明在加载的胫骨中,这些位置与年轻对照骨骼的加载诱导相似性为 89%。因此,这些数据表明,我们的方法能够识别特定骨骼年龄的一般预后表型,以及对所研究的小鼠胫骨和腓骨的这种明显骨骼年龄的时间和局部加载治疗效果。该方法的未来转化应用可能为骨质疏松症治疗提供一种相对低成本的改进决策支持方法。
骨骼是一种高度复杂和动态的结构,在衰老过程中以及对外界刺激(如加载)的反应中会发生变化。骨骼“年龄”和“状态”的自动评估可能导致骨质疏松症等疾病的早期预后,并能够评估某些治疗方法的效果。在这里,我们提出了一种基于人工智能的方法,能够以 95%的准确度从 μCT 图像中自动预测骨骼年龄。此外,我们利用它来证明体内加载治疗对骨骼的再生作用。我们进一步,首次通过定量分析“年龄评估模型学到了什么”来分解与年龄相关的骨骼局部变化,并利用这些信息来研究再生过程的结构细节。