A Comprehensive Evaluation of Multiple Enlarged Perivascular Space Segmentation Tools

Abstract Background Enlarged perivascular spaces (ePVS) are a marker of cerebral small vessel disease (SVD) detectable on magnetic resonance imaging (MRI). Due to their small size, diffuse distribution, and similar appearance to other markers of SVD, ePVS are inherently difficult to quantify on MRI, resulting in a lack of reliable quantification methods. We comprehensively evaluated and tested several automated ePVS segmentation algorithms by comparing their detection and segmentation performances to gold standard manual tracings. Method Vanderbilt Memory and Aging Project participants ( n = 30, 72.2±8.8 years, 47% female) underwent T1‐weighted, T2‐weighted, and fluid‐attenuated inversion recovery 3T MRI, and were manually traced by a neuroradiologist to measure ePVS burden. Five algorithms were used to segment ePVS on all participants: BigrBrain, SHIVA‐T1, MAPS‐T1, SegCSVD, and a locally developed nnU‐Net, Detection and Output of enlaRged pErivascular Spaces (DORES). To assess algorithm detection and segmentation capabilities, the Dice score, F1 score, absolute volume difference (AVD), and absolute element difference (AED) were calculated and compared against the expert manual rater separately for the basal ganglia and white matter. Result The algorithm with the highest overall performance was DORES, followed by SegCSVD. In the basal ganglia, the DORES achieved a Dice score of 0.73±0.09, F1 score of 0.72±0.10, AVD of 88±120, and AED of 29±33. SegCSVD, by contrast, achieved a Dice score of 0.56±0.09, F1 score of 0.52±0.08, AVD of 109±58, and AED of 52±53. In the white matter, DORES achieved a Dice score of 0.63±0.17, F1 score of 0.68±0.16, AVD of 327±629, and AED of 68±79. By comparison, SegCSVD achieved a Dice score of 0.39±0.18, an F1 score of 0.39±0.18, an AVD of 380±643, and an AED of 135±127 in the white matter. Conclusion We present a new deep‐learning algorithm, DORES, as an effective tool for segmenting ePVS in our cohort. Compared to other algorithms, DORES demonstrated higher accuracy, agreement, and validity across metrics of detection, segmentation, and correlations with manual tracings in both basal ganglia and white matter.

Authors

Institutions

Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70856_106612
Primary Topic
Cerebrospinal fluid and hydrocephalus
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Comprehensive Evaluation of Multiple Enlarged Perivascular Space Segmentation Tools

Niranjana Shashikumar, D. Liu, Yukti Vyas, Bennett A. Landman et al.
Alzheimer s & Dementia
Cerebrospinal fluid and hydrocephalus
article

A Comprehensive Evaluation of Multiple Enlarged Perivascular Space Segmentation Tools

Niranjana Shashikumar, D. Liu, Yukti Vyas, Bennett A. Landman, L. Taylor Davis, W Hudson Robb, T. Bryan Jackson, Angela L. Jefferson, James D LeFevre
article en

Abstract

Abstract Background Enlarged perivascular spaces (ePVS) are a marker of cerebral small vessel disease (SVD) detectable on magnetic resonance imaging (MRI). Due to their small size, diffuse distribution, and similar appearance to other markers of SVD, ePVS are inherently difficult to quantify on MRI, resulting in a lack of reliable quantification methods. We comprehensively evaluated and tested several automated ePVS segmentation algorithms by comparing their detection and segmentation performances to gold standard manual tracings. Method Vanderbilt Memory and Aging Project participants ( n = 30, 72.2±8.8 years, 47% female) underwent T1‐weighted, T2‐weighted, and fluid‐attenuated inversion recovery 3T MRI, and were manually traced by a neuroradiologist to measure ePVS burden. Five algorithms were used to segment ePVS on all participants: BigrBrain, SHIVA‐T1, MAPS‐T1, SegCSVD, and a locally developed nnU‐Net, Detection and Output of enlaRged pErivascular Spaces (DORES). To assess algorithm detection and segmentation capabilities, the Dice score, F1 score, absolute volume difference (AVD), and absolute element difference (AED) were calculated and compared against the expert manual rater separately for the basal ganglia and white matter. Result The algorithm with the highest overall performance was DORES, followed by SegCSVD. In the basal ganglia, the DORES achieved a Dice score of 0.73±0.09, F1 score of 0.72±0.10, AVD of 88±120, and AED of 29±33. SegCSVD, by contrast, achieved a Dice score of 0.56±0.09, F1 score of 0.52±0.08, AVD of 109±58, and AED of 52±53. In the white matter, DORES achieved a Dice score of 0.63±0.17, F1 score of 0.68±0.16, AVD of 327±629, and AED of 68±79. By comparison, SegCSVD achieved a Dice score of 0.39±0.18, an F1 score of 0.39±0.18, an AVD of 380±643, and an AED of 135±127 in the white matter. Conclusion We present a new deep‐learning algorithm, DORES, as an effective tool for segmenting ePVS in our cohort. Compared to other algorithms, DORES demonstrated higher accuracy, agreement, and validity across metrics of detection, segmentation, and correlations with manual tracings in both basal ganglia and white matter.

Alzheimer s & DementiaVol. 21(S2)
Vanderbilt University (US), Vanderbilt University Medical Center (US)
Gender equality
Openalex Percentile: Top 35%
Cerebrospinal fluid and hydrocephalus
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.