Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, USA; Department of Orthopedic Surgery, Mayo Clinic, Rochester, MN, USA.
Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, USA; Department of Orthopedic Surgery, Mayo Clinic, Rochester, MN, USA.
Comput Biol Med. 2021 Oct;137:104833. doi: 10.1016/j.compbiomed.2021.104833. Epub 2021 Sep 9.
Osteoporosis-related vertebral compression fracture can occur under normal physiological activities. Bone metastasis is another source of vertebral fracture. Different loading rates, either high-energy traumas such as falls or low-energy traumas under normal physiological activities, can result in different fracture outcomes. The aim of the current study was to develop a quantitative computed tomography-based finite element analysis (QCT/FEA) technique for single vertebral bodies to predict fracture strength of three-level spine segments. Developed QCT/FEA technique was also used to characterize vertebral elastic moduli at two loading rates of 5 mm/min, representing a physiologic loading condition, and 12000 mm/min, representing a high-energy trauma. To this end, a cohort of human spine segments divided into three groups of intact, defect, and augmented were mechanically tested to fracture; then, experimental stiffness and fracture strength values were measured. Outcomes of this study showed no significant difference between the elastic modulus equations at the two testing speeds. Areal bone mineral density measured by dual x-ray absorptiometry (DXA/BMD) explained only 53% variability (R = 0.53) in fracture strength outcomes. However, QCT/FEA could explain 70% of the variability (R = 0.70) in experimentally measured fracture strength values. Adding disk degeneration grading, testing speed, and sex to QCT/FEA-estimated fracture strength values further increased the performance of our statistical model by 14% (adjusted R of 0.84 between the prediction and experimental fracture forces). In summary, our results indicated that a single-vertebra model, which is computationally less expensive and more time efficient, is capable of estimating fracture outcomes with acceptable performance (range: 70-84%).
骨质疏松性椎体压缩性骨折可在正常生理活动下发生。骨转移是另一种导致椎体骨折的原因。不同的加载速率,无论是高能量创伤如跌倒还是正常生理活动下的低能量创伤,都可能导致不同的骨折结果。本研究的目的是开发一种基于定量 CT 的有限元分析(QCT/FEA)技术,用于单椎体,以预测三级脊柱段的骨折强度。还使用开发的 QCT/FEA 技术来描述两种加载速率下的椎体弹性模量,分别为 5mm/min,代表生理加载条件,以及 12000mm/min,代表高能量创伤。为此,一组人类脊柱段分为完整、缺陷和增强三组进行机械测试至骨折;然后,测量实验刚度和骨折强度值。该研究的结果表明,两种测试速度下的弹性模量方程没有显著差异。双能 X 线吸收法(DXA/BMD)测量的面积骨密度仅解释了骨折强度结果的 53%(R=0.53)的可变性。然而,QCT/FEA 可以解释 70%的实验测量的骨折强度值的可变性(R=0.70)。将椎间盘退变分级、测试速度和性别添加到 QCT/FEA 估计的骨折强度值中,进一步将我们的统计模型的性能提高了 14%(预测和实验骨折力之间的调整 R 为 0.84)。总之,我们的结果表明,单椎体模型计算成本较低,效率更高,能够以可接受的性能(范围:70-84%)估计骨折结果。