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OMIBONE: Omics-driven computer model of bone regeneration for personalized treatment
Citation Link: https://doi.org/10.15480/882.14878
Publikationstyp
Journal Article
Date Issued
2024-10-18
Sprache
English
Author(s)
TORE-DOI
Journal
Volume
190
Article Number
117288
Citation
Bone 190: 117288 (2025)
Publisher DOI
Scopus ID
ISSN
87563282
Treatment of bone fractures are standardized according to the AO classification, which mainly refers to the mechanical stabilization required in a given situation but neglect individual differences due to patient's healing potential or accompanying diseases. Specially in elderly or immune-compromised patients, the complexity of individual constrains on a biological as well as mechanical level are hard to account for. Here, we introduce a novel framework that allows to predict bone regeneration outcome using combined proteomic and mechanical analyses in a computer model. The framework uses Ingenuity Pathway Analysis (IPA) software to link protein changes to alterations in biological processes and integrates these in an Agent-Based Model (ABM) of bone regeneration. This combined framework allows to predict bone formation and the potential of an individual to heal a given fracture setting. The performance of the framework was evaluated by replicating the experimental setup of a mouse femur fracture stabilized with an intramedullary pin. The model was informed by serum derived proteomics data. The tissue formation patterns were compared against experimental data based on x-ray and histology images. The results indicate the framework potential in predicting an individual's bone formation potential and hold promise as a concept to enable personalized bone healing predictions for a chosen fracture fixation.
Subjects
Agent Based Model (ABM)
Bone regeneration
Computational modeling
Ingenuity Pathway Analysis (IPA)
Personalized treatment
Proteomics
DDC Class
600: Technology
Publication version
publishedVersion
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1-s2.0-S8756328224002771-main.pdf
Type
Main Article
Size
6.8 MB
Format
Adobe PDF