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An in silico micro-multiphysics agent-based approach for simulating bone regeneration in a mouse femur defect model.
Kendall, Jack J; Ledoux, Charles; Marques, Francisco C; Boaretti, Daniele; Schulte, Friederike A; Morgan, Elise F; Müller, Ralph.
Afiliación
  • Kendall JJ; Institute for Biomechanics, ETH Zurich, Zurich, Switzerland.
  • Ledoux C; Center for Multiscale and Translational Mechanobiology, Boston University, Boston, MA, United States.
  • Marques FC; Institute for Biomechanics, ETH Zurich, Zurich, Switzerland.
  • Boaretti D; Institute for Biomechanics, ETH Zurich, Zurich, Switzerland.
  • Schulte FA; Institute for Biomechanics, ETH Zurich, Zurich, Switzerland.
  • Morgan EF; Institute for Biomechanics, ETH Zurich, Zurich, Switzerland.
  • Müller R; Center for Multiscale and Translational Mechanobiology, Boston University, Boston, MA, United States.
Front Bioeng Biotechnol ; 11: 1289127, 2023.
Article en En | MEDLINE | ID: mdl-38164405
ABSTRACT
Bone defects represent a challenging clinical problem as they can lead to non-union. In silico models are well suited to study bone regeneration under varying conditions by linking both cellular and systems scales. This paper presents an in silico micro-multiphysics agent-based (micro-MPA) model for bone regeneration following an osteotomy. The model includes vasculature, bone, and immune cells, as well as their interaction with the local environment. The model was calibrated by time-lapsed micro-computed tomography data of femoral osteotomies in C57Bl/6J mice, and the differences between predicted bone volume fractions and the longitudinal in vivo measurements were quantitatively evaluated using root mean square error (RMSE). The model performed well in simulating bone regeneration across the osteotomy gap, with no difference (5.5% RMSE, p = 0.68) between the in silico and in vivo groups for the 5-week healing period - from the inflammatory phase to the remodelling phase - in the volume spanning the osteotomy gap. Overall, the proposed micro-MPA model was able to simulate the influence of the local mechanical environment on bone regeneration, and both this environment and cytokine concentrations were found to be key factors in promoting bone regeneration. Further, the validated model matched clinical observations that larger gap sizes correlate with worse healing outcomes and ultimately simulated non-union. This model could help design and guide future experimental studies in bone repair, by identifying which are the most critical in vivo experiments to perform.
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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Bioeng Biotechnol Año: 2023 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Bioeng Biotechnol Año: 2023 Tipo del documento: Article País de afiliación: Suiza