segcsvd PVS : A Convolutional Neural Network‐Based Tool for Quantification of Enlarged Perivascular Spaces ( PVS ) on T 1 ‐Weighted Images

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Authors: Erin Gibson, Joel Ramirez, Lauren Abby Woods, Stephanie A. Berberian, Julie Ottoy, Christopher J.M. Scott, Vanessa Yhap, Fuqiang Gao, Roberto Duarte Coello, Maria del Carmen Valdés Hernández, Anthony Edward Lang, Maria Carmela Tartaglia
+12 more Sanjeev Kumar, Malcolm A. Binns, Robert Bartha, Sean P. Symons, Richard H. Swartz, Mario Masellis, Navneet Singh, Bradley J. MacIntosh, Joanna Marguerite Wardlaw, Sandra E. Black, Andrew S. P. Lim, Maged Goubran
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References: 16

Abstract

ABSTRACT Enlarged perivascular spaces (PVS) are imaging markers of cerebral small vessel disease (CSVD) that are associated with age, disease phenotypes, and overall health. Quantification of PVS is challenging but necessary to expand an understanding of their role in cerebrovascular pathology. Accurate and automated segmentation of PVS on T 1 ‐weighted images would be valuable given the widespread use of T 1 ‐weighted imaging protocols in multisite clinical and research datasets. We introduce segcsvd PVS , a convolutional neural network (CNN)‐based tool for automated PVS segmentation on T 1 ‐weighted images. segcsvd PVS was developed using a novel hierarchical approach that builds on existing tools and incorporates robust training strategies to enhance the accuracy and consistency of PVS segmentation. Performance was evaluated using a comprehensive evaluation strategy that included comparison to existing benchmark methods, ablation‐based validation, accuracy validation against manual ground truth annotations, correlation with age‐related PVS burden as a biological benchmark, and extensive robustness testing. segcsvd PVS achieved strong object‐level performance for basal ganglia PVS (DSC = 0.78), exhibiting both high sensitivity (SNS = 0.80) and precision (PRC = 0.78). Although voxel‐level precision was lower (PRC = 0.57), manual correction improved this by only ~3%, indicating that the additional voxels reflected primary boundary‐ or extent‐related differences rather than correctable false positive error. For non‐basal ganglia PVS, segcsvd PVS outperformed benchmark methods, exhibiting higher voxel‐level performance across several metrics (DSC = 0.60, SNS = 0.67, PRC = 0.57, NSD = 0.77), despite overall lower performance relative to basal ganglia PVS. Additionally, the association between age and segmentation‐derived measures of PVS burden was consistently stronger and more reliable for segcsvd PVS compared to benchmark methods across three cohorts (test6, ADNI, CAHHM), providing further evidence of the accuracy and consistency of its segmentation output. segcsvd PVS demonstrates robust performance across diverse imaging conditions and improved sensitivity to biologically meaningful associations, supporting its utility as a T 1 ‐based PVS segmentation tool.

Fields of Study & Subjects

Medical Image Segmentation Techniques Retinal Imaging and Analysis Cerebrovascular and genetic disorders

Publication details

Journal / source
Human Brain Mapping
Volume
47
Issue
2
Pages
e70462–e70462
Publication date
1 February 2026
Language
EN