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Darvishi, V.

Publications and source records attributed to Darvishi, V..

2 recordsLinked to original sources

PARS: an automated, open-source pipeline for subject-specific finite element head modelling from MRI

Converting medical images into anatomically detailed, subject-specific finite element (FE) models is a long-standing bottleneck in brain computational modelling. These models are used to predict brain tissue deformation, e.g. in traumatic brain injury, particle diffusion in brain drug delivery, and other biophysical phenomena across neurological disorders. However, existing model creation workflows depend on manual image segmentation, proprietary meshing software, and labourintensive repair of meningeal and interface structures, limiting reproducibility and cohort analysis. Here we present PARS, a fully automated, open-source pipeline that converts a T1-weighted MRI scan into a simulation-ready FE head model. PARS combines anatomical parcellation with tissue maps and uses iterative neighbourhood-based reclassification, yielding a gap-free whole-head label volume. The volume is directly converted into a hexahedral mesh, augmented with algorithmically reconstructed falx, tentorium, pia and dura mater, and refined by Laplacian smoothing under a node-locking scheme that controls element quality and the explicit-solver stable timestep. We evaluated PARS on 23 subjects spanning cranial volumes of 832-1,329 cm3, at 1.0, 1.5 and 2.0 mm MRI resolutions. At 1 mm, meshes achieved a median Scaled Jacobian of 0.976{+/-}0.012, and total intracranial volume error of 0.54{+/-}0.19%; quality remained high at 1.5 mm (SJ: 0.933{+/-}0.018) and 2 mm (SJ: 0.921{+/-}0.016). Model creation runtime ranged from 9 to 38 minutes per subject. Models generated by PARS have been validated against cadaveric brain displacement data and demonstrated utility across traumatic brain injury and normal pressure hydrocephalus research. PARS provides an open-access, reproducible resource that substantially lowers the barriers to subject-specific brain modelling.

bioengineering↗

Patient-informed biomechanical modelling reveals mechanical mechanism of brain damage in idiopathic normal pressure hydrocephalus

Idiopathic normal pressure hydrocephalus (iNPH) is a globally growing neurological disorder in older adults, radiologically characterised by enlargement of ventricles. However, it remains unknown whether ventricular enlargement can produce biomechanical loading large enough to drive brain morphological changes and tissue damage. Here, we develop an anatomically detailed biomechanical model of ageing human brain and apply ventricular enlargement using a three-dimensional displacement field derived from MRI of iNPH patients and age-matched controls. The model accurately reproduces radiological markers of iNPH, including Evans index, callosal angle and high-convexity sulcal narrowing. It further predicts large mechanical strains in periventricular white matter, particularly within the corpus callosum and anterior thalamic radiations, tracts consistently implicated in iNPH imaging abnormalities. These findings provide strong evidence that ventricular enlargement induces mechanical strain that contributes to iNPH brain abnormalities, which can potentially be reversed by reducing strain following shunting surgery. The biomechanical brain model forms the foundation of a predictive digital platform and future "digital twin" technology to support diagnosis, patient stratification and treatment planning in iNPH. Key PointsO_LIWe develop an anatomically detailed biomechanical model of the brain, incorporating sulci, septum pellucidum and all four ventricles. C_LIO_LIA novel data-driven loading approach is introduced which uses 3D displacement fields from finite element-based registration of healthy and iNPH patient MRI, replacing the arbitrary pressure gradients of previous models. C_LIO_LIThe model predictions closely match established radiological markers measured in iNPH patients, including Evans index, callosal angle and high-convexity sulcal narrowing. C_LIO_LIVentricular enlargement generates large mechanical strains concentrated in periventricular white matter, providing a biomechanical explanation for the structural abnormalities observed in iNPH. C_LI

bioengineering↗