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A Photopolymerizable Hyaluronic Acid-Collagen Model of the Invasive Glioma Microenvironment with Interstitial Flow
Published on: October 18, 2024
Comparing finite elements and finite differences for developing diffusive models of glioma growth
Alexandros Roniotis1, Kostas Marias, Vangelis Sakkalis
1Institute of Computer Science, Foundation for Research and Technology (FORTH), Heraklion 71110, Greece. roniotis@ics.forth.gr
Summary
This study compares finite element (FE) and finite difference (FD) methods for simulating glioma brain tumor growth. Results show how mesh variations impact computational accuracy and efficiency in these diffusion-reaction models.
Area of Science:
- Computational biology
- Mathematical oncology
- Biomedical modeling
Background:
- Glioma, an aggressive brain tumor, necessitates accurate mathematical models for understanding its development.
- Diffusion-reaction equations (DREs) are commonly employed to simulate glioma's spatiotemporal cell concentration dynamics.
- Finite difference (FD) and finite element (FE) methods are prevalent numerical techniques for solving DREs in these models.
Purpose of the Study:
- To experimentally compare the performance of finite element (FE) and finite difference (FD) methods in the context of glioma modeling.
- To investigate the influence of different brain mesh configurations on the computational consistency, simulation time, and overall efficiency of DRE-based glioma models.
Main Methods:
- Implementation and comparison of FE and FD numerical methods for solving the diffusion-reaction equation.
- Experimental analysis using a glioma model with a known analytical solution to quantify errors.
- Evaluation of computational consistency, simulation duration, and model efficiency across varying mesh structures.
Main Results:
- The study presents experimental findings comparing the accuracy and efficiency of FE and FD methods for glioma simulation.
- Variations in brain mesh resolution significantly affect the computational performance and consistency of the models.
- Quantifiable error metrics were calculated for both methods using a validated test case.
Conclusions:
- Both FE and FD methods offer viable approaches for simulating glioma progression, with performance influenced by mesh strategy.
- Understanding the trade-offs between mesh complexity, computational cost, and accuracy is crucial for selecting appropriate numerical methods.
- This comparative analysis provides valuable insights for developing more efficient and accurate computational tools for glioma research.

