Savelli Giacomo, Oliviero Sara, La Mattina Antonino A, Viceconti Marco
Department of Industrial Engineering, Alma Mater Studiorum - University of Bologna, Bologna, Italy.
Medical Technology Lab, IRCSS - Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136, Bologna, Italy.
Ann Biomed Eng. 2025 Mar;53(3):578-587. doi: 10.1007/s10439-024-03636-4. Epub 2024 Nov 22.
Osteoporosis represents a major healthcare concern. The development of novel treatments presents challenges due to the limited cost-effectiveness of clinical trials and ethical concerns associated with placebo-controlled trials. Computational models for the design and assessment of biomedical products (In Silico Trials) are emerging as a promising alternative. In this study, a novel In Silico Trial technology (BoneStrength) was applied to replicate the placebo arms of two concluded clinical trials and its accuracy in predicting hip fracture incidence was evaluated. Two virtual cohorts (N = 1238 and 1226, respectively) were generated by sampling a statistical anatomy atlas based on CT scans of proximal femurs. Baseline characteristics were equivalent to those reported for the clinical cohorts. Fall events were sampled from a Poisson distribution. A multiscale stochastic model was implemented to estimate the impact force associated to each fall. Finite Element models were used to predict femur strength. Fracture incidence in 3 years follow-up was computed with a Markov chain approach; a patient was considered fractured if the impact force associated with a fall exceeded femur strength. Ten realizations of the stochastic process were run to reach convergence. Each realization required approximately 2500 FE simulations, solved using High-Performance Computing infrastructures. Predicted number of fractures was 12 ± 2 and 18 ± 4 for the two cohorts, respectively. The predicted incidence range consistently included the reported clinical data, although on average fracture incidence was overestimated. These findings highlight the potential of BoneStrength for future applications in drug development and assessment.
骨质疏松症是一个重大的医疗保健问题。由于临床试验的成本效益有限以及与安慰剂对照试验相关的伦理问题,新型治疗方法的开发面临挑战。用于生物医学产品设计和评估的计算模型(计算机模拟试验)正成为一种有前途的替代方法。在本研究中,一种新型的计算机模拟试验技术(骨强度)被应用于复制两项已完成临床试验的安慰剂组,并评估其预测髋部骨折发生率的准确性。通过对基于股骨近端CT扫描的统计解剖图谱进行采样,生成了两个虚拟队列(分别为N = 1238和1226)。基线特征与临床队列报告的特征相当。跌倒事件从泊松分布中采样。实施了一个多尺度随机模型来估计每次跌倒相关的冲击力。使用有限元模型来预测股骨强度。采用马尔可夫链方法计算3年随访中的骨折发生率;如果与跌倒相关的冲击力超过股骨强度,则认为患者发生骨折。运行随机过程的十次实现以达到收敛。每次实现大约需要2500次有限元模拟,使用高性能计算基础设施进行求解。两个队列预测的骨折数量分别为12±2和18±4。尽管平均骨折发生率被高估,但预测的发生率范围始终包括报告的临床数据。这些发现突出了骨强度在未来药物开发和评估中的应用潜力。