Suhyun Ahn

Wonjung Park, Suhyun Ahn, Jinah Park

Lateral ventricle (LV) shape analysis holds promise as a biomarker for neurological diseases; however, challenges remain due to substantial shape variability across individuals and segmentation difficulties arising from limited MRI resolution. We introduce LV-Net, a novel framework for producing individualized 3D LV meshes from brain MRI by deforming an anatomy-aware joint LV-hippocampus template mesh. By incorporating anatomical relationships embedded within the joint template, LV-Net reduces boundary segmentation artifacts and improves reconstruction robustness. In addition, by classifying the vertices of the template mesh based on their anatomical adjacency, our method enhances point correspondence across subjects, leading to more accurate LV shape statistics. We demonstrate that LV-Net achieves superior reconstruction accuracy, even in the presence of segmentation imperfections, and delivers more reliable shape descriptors across diverse datasets. Finally, we apply LV-Net to Alzheimer's disease analysis, identifying LV subregions that show significantly associations with the disease relative to cognitively normal controls. The codes for LV shape modeling are available at https://github.com/PWonjung/LV_Shape_Modeling.

Wonjung Park, Suhyun Ahn, Jinah Park

The deformation of the lateral ventricle (LV) shape is widely studied to identify specific morphometric changes associated with diseases. Since LV enlargement is considered a relative change due to brain atrophy, local longitudinal LV deformation can indicate deformation in adjacent brain areas. However, conventional methods for LV shape analysis focus on modeling the solely segmented LV mask. In this work, we propose a novel deep learning-based approach using peripheral area projection, which is the first attempt to analyze LV considering its surrounding areas. Our approach matches the baseline LV mesh by deforming the shape of follow-up LVs, while optimizing the corresponding points of the same adjacent brain area between the baseline and follow-up LVs. Furthermore, we quantitatively evaluated the deformation of the left LV in normal (n=10) and demented subjects (n=10), and we found that each surrounding area (thalamus, caudate, hippocampus, amygdala, and right LV) projected onto the surface of LV shows noticeable differences between normal and demented subjects.