4.5 Article

Embedded axonal fiber tracts improve finite element model predictions of traumatic brain injury

期刊

BIOMECHANICS AND MODELING IN MECHANOBIOLOGY
卷 19, 期 3, 页码 1109-1130

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s10237-019-01273-8

关键词

Multi-scale finite element modeling; Axonal injury prediction; Diffusion tensor imaging; Tractography; Axonal tract network

资金

  1. NIH HHS [R56NS055951, R01NS097549] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS097549, R56 NS055951] Funding Source: Medline

向作者/读者索取更多资源

With the growing rate of traumatic brain injury (TBI), there is an increasing interest in validated tools to predict and prevent brain injuries. Finite element models (FEM) are valuable tools to estimate tissue responses, predict probability of TBI, and guide the development of safety equipment. In this study, we developed and validated an anisotropic pig brain multi-scale FEM by explicitly embedding the axonal tract structures and utilized the model to simulate experimental TBI in piglets undergoing dynamic head rotations. Binary logistic regression, survival analysis with Weibull distribution, and receiver operating characteristic curve analysis, coupled with repeated k-fold cross-validation technique, were used to examine 12 FEM-derived metrics related to axonal/brain tissue strain and strain rate for predicting the presence or absence of traumatic axonal injury (TAI). All 12 metrics performed well in predicting of TAI with prediction accuracy rate of 73-90%. The axonal-based metrics outperformed their rival brain tissue-based metrics in predicting TAI. The best predictors of TAI were maximum axonal strain times strain rate (MASxSR) and its corresponding optimal fraction-based metric (AF-MASxSR(7.5)) that represents the fraction of axonal fibers exceeding MASxSR of 7.5 s(-1). The thresholds compare favorably with tissue tolerances found in in-vitro/in-vivo measurements in the literature. In addition, the damaged volume fractions (DVF) predicted using the axonal-based metrics, especially MASxSR (DVF = 0.05-4.5%), were closer to the actual DVF obtained from histopathology (AIV = 0.02-1.65%) in comparison with the DVF predicted using the brain-related metrics (DVF = 0.11-41.2%). The methods and the results from this study can be used to improve model prediction of TBI in humans.

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