A robust automated segmentation method for white matter hyperintensity of vascular-origin

White matter hyperintensity (WMH) is a primary manifestation of small vessel disease (SVD), leading to vascular cognitive impairment and other disorders. Accurate WMH quantification is vital for diagnosis and prognosis, but current automatic segmentation methods often fall short, especially across different datasets. The aims of this study are to develop and validate a robust deep learning segmentation method for WMH of vascular-origin. In this study, we developed a transformer-based method for the automatic segmentation of vascular-origin WMH using both 3D T1 and 3D T2-FLAIR images. Our initial dataset comprised 126 participants with varying WMH burdens due to SVD, each with manually segmented WMH masks used for training and testing. External validation was performed on two independent datasets: the WMH Segmentation Challenge 2017 dataset (170 subjects) and an in-house vascular risk factor dataset (70 subjects), which included scans acquired on eight different MRI systems at field strengths of 1.5T, 3T, and 5T This approach enabled a comprehensive assessment of the method's generalizability across diverse imaging conditions. We further compared our method against LGA, LPA, BIANCA, UBO-detector and TrUE-Net in optimized settings. Our method consistently outperformed others, achieving a median Dice coefficient of 0.78 ± 0.09 in our primary dataset, 0.72 ± 0.15 in the external dataset 1, and 0.72 ± 0.14 in the external dataset 2. The relative volume errors were 0.15 ± 0.14, 0.50 ± 0.86, and 0.47 ± 1.02, respectively. The true positive rates were 0.81 ± 0.13, 0.92 ± 0.09, and 0.92 ± 0.12, while the false positive rates were 0.20 ± 0.09, 0.40 ± 0.18, and 0.40 ± 0.19. None of the external validation datasets were used for model training; instead, they comprise previously unseen MRI scans acquired from different scanners and protocols. This setup closely reflects real-world clinical scenarios and further demonstrates the robustness and generalizability of our model across diverse MRI systems and acquisition settings. As such, the proposed method provides a reliable solution for WMH segmentation in large-scale cohort studies.

Authors

Institutions

Publication Details

Journal
NeuroImage
Published
2025-05-17
DOI
https://doi.org/10.1016/j.neuroimage.2025.121279
Primary Topic
Cerebrovascular and Carotid Artery Diseases
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A robust automated segmentation method for white matter hyperintensity of vascular-origin

Junjian Zhang, Shenjia Wu, Jiu Jiang, Haoying He et al.
NeuroImage
Cerebrovascular and Carotid Artery Diseases
article

A robust automated segmentation method for white matter hyperintensity of vascular-origin

Junjian Zhang, Shenjia Wu, Jiu Jiang, Haoying He, Fan Fan, T. Sun, Chu He, Dong Sun, Zhipeng Xu, Sisi Peng, Hao Song, Dongwei Lu
article en

Abstract

White matter hyperintensity (WMH) is a primary manifestation of small vessel disease (SVD), leading to vascular cognitive impairment and other disorders. Accurate WMH quantification is vital for diagnosis and prognosis, but current automatic segmentation methods often fall short, especially across different datasets. The aims of this study are to develop and validate a robust deep learning segmentation method for WMH of vascular-origin. In this study, we developed a transformer-based method for the automatic segmentation of vascular-origin WMH using both 3D T1 and 3D T2-FLAIR images. Our initial dataset comprised 126 participants with varying WMH burdens due to SVD, each with manually segmented WMH masks used for training and testing. External validation was performed on two independent datasets: the WMH Segmentation Challenge 2017 dataset (170 subjects) and an in-house vascular risk factor dataset (70 subjects), which included scans acquired on eight different MRI systems at field strengths of 1.5T, 3T, and 5T This approach enabled a comprehensive assessment of the method's generalizability across diverse imaging conditions. We further compared our method against LGA, LPA, BIANCA, UBO-detector and TrUE-Net in optimized settings. Our method consistently outperformed others, achieving a median Dice coefficient of 0.78 ± 0.09 in our primary dataset, 0.72 ± 0.15 in the external dataset 1, and 0.72 ± 0.14 in the external dataset 2. The relative volume errors were 0.15 ± 0.14, 0.50 ± 0.86, and 0.47 ± 1.02, respectively. The true positive rates were 0.81 ± 0.13, 0.92 ± 0.09, and 0.92 ± 0.12, while the false positive rates were 0.20 ± 0.09, 0.40 ± 0.18, and 0.40 ± 0.19. None of the external validation datasets were used for model training; instead, they comprise previously unseen MRI scans acquired from different scanners and protocols. This setup closely reflects real-world clinical scenarios and further demonstrates the robustness and generalizability of our model across diverse MRI systems and acquisition settings. As such, the proposed method provides a reliable solution for WMH segmentation in large-scale cohort studies.

NeuroImageVol. 315
Wuhan University (CN), Zhongnan Hospital of Wuhan University (CN), Wuchang University of Technology (CN)
Zero hunger
Openalex Percentile: Top 82%
Cerebrovascular and Carotid Artery Diseases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.