Abstract

Fragility fractures are a major socioeconomic problem. A non-invasive, computationally-efficient method for the identification of fracture risk scenarios under the representation of neuro-musculoskeletal dynamics does not exist. We introduce a computational workflow that integrates modally-reduced, quantitative CT-based finite-element models into neuro-musculoskeletal flexible multibody simulation (NfMBS) for early bone fracture risk assessment. Our workflow quantifies the bone strength via the osteogenic stresses and strains that arise due to the physiological-like loading of the bone under the representation of patient-specific neuro-musculoskeletal dynamics. This allows for non-invasive, computationally-efficient dynamic analysis over the enormous parameter space of fracture risk scenarios, while requiring only sparse clinical data. Experimental validation on a fresh human femur specimen together with femur strength computations that were consistent with literature findings provide confidence in the workflow: The simulation of an entire squat took only 38 s CPU-time. Owing to the loss (16% cortical, 33% trabecular) of bone mineral density (BMD), the strain measure that is associated with bone fracture increased by 31.4%; and yielded an elevated risk of a femoral hip fracture. Our novel workflow could offer clinicians with decision-making guidance by enabling the first combined in-silico analysis tool using NfMBS and BMD measurements for optimized bone fracture risk assessment.

Highlights

  • It is of major importance to reliably and rapidly obtain information on the dynamic in-vivo bone stresses and strains as these are fundamental parameters in mechanostat theory that characterizes the interplay between dynamic mechanical loading and musculoskeletal health[1]: Dynamic bone stresses and strains control bone remodeling[2,3] are indicators of bone fractures[2,4,5] and allow for tailored and monitored clinical treatment[6]

  • We modeled osteoporotic bone as described by Little and coworkers[46], which provided insight into the change of osteogenic parameters during dynamic squat motion for the fracture risk assessment after bone mineral density (BMD)-loss leading to osteoporotic conditions in the previously analyzed femur specimen

  • It has been shown that patient-specific finite-element analysis (FEA) that utilizes quantitative CT (QCT) for material property identification is beneficial over dual-energy X-ray absorptiometry-based (DXA)-based BMD measurement for diagnosis and medication effect assessment in osteoporotic patients[2,3,29,30]

Read more

Summary

Introduction

It is of major importance to reliably and rapidly obtain information on the dynamic in-vivo bone stresses and strains as these are fundamental parameters in mechanostat theory that characterizes the interplay between dynamic mechanical loading and musculoskeletal health[1]: Dynamic bone stresses and strains control bone remodeling[2,3] are indicators of bone fractures[2,4,5] and allow for tailored and monitored clinical treatment[6]. Finite-element analysis (FEA) has been used extensively to address musculoskeletal research questions by means of non-invasive computational analysis; e.g., to study the mechanical behavior of human bones[13,15,16,17,18], bone remodeling[19,20,21], bone adaption[22,23] and/or to estimate the progression of osteoarthritis in normal and overweight subjects[24,25,26] Thereby, it has become a state-of-the-art method to assign the Hounsfield units (HU) of computed tomography (CT) imaging data to the finite-element mesh to capture the patient-specific bone density distribution[14,17]. Another application of these NMBS is the extraction of boundary conditions for FEA23 or the co-simulation of FEA and NMBS that can be used to investigate, for e.g., the effects of gait modifications[39,40]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call