Application of subject-specific adaptive mechanical loading for bone healing in a mouse tail vertebral defect

Sci Rep. 2021 Jan 21;11(1):1861. doi: 10.1038/s41598-021-81132-8.

Abstract

Methods to repair bone defects arising from trauma, resection, or disease, continue to be sought after. Cyclic mechanical loading is well established to influence bone (re)modelling activity, in which bone formation and resorption are correlated to micro-scale strain. Based on this, the application of mechanical stimulation across a bone defect could improve healing. However, if ignoring the mechanical integrity of defected bone, loading regimes have a high potential to either cause damage or be ineffective. This study explores real-time finite element (rtFE) methods that use three-dimensional structural analyses from micro-computed tomography images to estimate effective peak cyclic loads in a subject-specific and time-dependent manner. It demonstrates the concept in a cyclically loaded mouse caudal vertebral bone defect model. Using rtFE analysis combined with adaptive mechanical loading, mouse bone healing was significantly improved over non-loaded controls, with no incidence of vertebral fractures. Such rtFE-driven adaptive loading regimes demonstrated here could be relevant to clinical bone defect healing scenarios, where mechanical loading can become patient-specific and more efficacious. This is achieved by accounting for initial bone defect conditions and spatio-temporal healing, both being factors that are always unique to the patient.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological / physiology
  • Animals
  • Coccyx / diagnostic imaging
  • Coccyx / injuries*
  • Disease Models, Animal
  • Female
  • Finite Element Analysis
  • Fracture Healing / physiology*
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Osteogenesis / physiology
  • Spinal Fractures / diagnostic imaging
  • Spinal Fractures / physiopathology*
  • Stress, Mechanical*
  • Tail
  • Weight-Bearing / physiology*
  • X-Ray Microtomography / methods