<scp> segcsvd <sub>WMH</sub> </scp> : A Convolutional Neural Network‐Based Tool for Quantifying White Matter Hyperintensities in Heterogeneous Patient Cohorts

White matter hyperintensities (WMH) of presumed vascular origin are a magnetic resonance imaging (MRI)-based biomarker of cerebral small vessel disease (CSVD). WMH are associated with cognitive decline and increased risk of stroke and dementia, and are commonly observed in aging, vascular cognitive impairment, and neurodegenerative diseases. The reliable and rapid measurement of WMH in large-scale multisite clinical studies with heterogeneous patient populations remains challenging, where the diversity of imaging characteristics across studies adds additional complexity to this task. We present segcsvd<sub>WMH</sub>, a convolutional neural network-based tool developed to provide reliable and accurate WMH quantification across diverse clinical datasets. segcsvd<sub>WMH</sub> was developed using a large dataset consisting of over 700 fluid-attenuated inversion recovery MRI scans from seven multisite studies, spanning a wide range of clinical populations, WMH burdens, and imaging protocols. Model training incorporated anatomical information through a novel hierarchical segmentation approach, together with extensive data augmentation techniques to improve performance across varied imaging conditions. Benchmarked against three widely available segmentation tools, segcsvd<sub>WMH</sub> demonstrated superior accuracy, achieving mean Dice score improvements of 7.8% ± 9.7% over HyperMapp3r, 21.8% ± 8.6% over SAMSEG, and 43.5% ± 7.1% over WMH-SynthSeg across four diverse test datasets. segcsvd<sub>WMH</sub> also maintained consistently high Dice scores across these test datasets (mean DSC = 0.86 ± 0.08), and exhibited strong, stable correlations with periventricular, deep, and total WMH ground truth volumes (mean r = 0.99 ± 0.01). Additionally, segcsvd<sub>WMH</sub> was robust to low and moderate levels of simulated MRI spike noise artifacts and maintained strong performance across a range of binary segmentation thresholds and WMH burden levels. These findings suggest that segcsvd<sub>WMH</sub> may provide more accurate and robust WMH segmentation performance for heterogeneous clinical datasets characterized by varying degrees of CSVD severity.

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Publication Details

Journal
Human Brain Mapping
Published
2024-12-15
DOI
https://doi.org/10.1002/hbm.70104
Citations
8
Primary Topic
Cerebrovascular and Carotid Artery Diseases
Type
article
Field-Weighted Citation Impact
3.35

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article

segcsvd WMH : A Convolutional Neural Network‐Based Tool for Quantifying White Matter Hyperintensities in Heterogeneous Patient Cohorts

Anthony E. Lang, Andrew Lim, Joanna Marguerite Wardlaw, Robert Bartha et al.
8 citations
Human Brain Mapping
Cerebrovascular and Carotid Artery Diseases
3.35
article

segcsvd WMH : A Convolutional Neural Network‐Based Tool for Quantifying White Matter Hyperintensities in Heterogeneous Patient Cohorts

Anthony E. Lang, Andrew Lim, Joanna Marguerite Wardlaw, Robert Bartha, Bradley J. MacIntosh, Maria del Carmen Valdés Hernández, Vanessa Yhap, Erin Gibson, Sandra E. Black, Maged Goubran, Sean Symons, Navneet Singh, Alan R. Moody, Julie Ottoy, Sanjeev Kumar, Malcolm A. Binns, Joel Ramirez, Stephanie Berberian, Roberto Duarte Coello, Christopher J.M. Scott, Fuqiang Gao, Maria Carmela Tartaglia, Lauren Abby Woods, Mario Masellis, Richard H. Swartz
article en
8 citations

Abstract

White matter hyperintensities (WMH) of presumed vascular origin are a magnetic resonance imaging (MRI)-based biomarker of cerebral small vessel disease (CSVD). WMH are associated with cognitive decline and increased risk of stroke and dementia, and are commonly observed in aging, vascular cognitive impairment, and neurodegenerative diseases. The reliable and rapid measurement of WMH in large-scale multisite clinical studies with heterogeneous patient populations remains challenging, where the diversity of imaging characteristics across studies adds additional complexity to this task. We present segcsvd<sub>WMH</sub>, a convolutional neural network-based tool developed to provide reliable and accurate WMH quantification across diverse clinical datasets. segcsvd<sub>WMH</sub> was developed using a large dataset consisting of over 700 fluid-attenuated inversion recovery MRI scans from seven multisite studies, spanning a wide range of clinical populations, WMH burdens, and imaging protocols. Model training incorporated anatomical information through a novel hierarchical segmentation approach, together with extensive data augmentation techniques to improve performance across varied imaging conditions. Benchmarked against three widely available segmentation tools, segcsvd<sub>WMH</sub> demonstrated superior accuracy, achieving mean Dice score improvements of 7.8% ± 9.7% over HyperMapp3r, 21.8% ± 8.6% over SAMSEG, and 43.5% ± 7.1% over WMH-SynthSeg across four diverse test datasets. segcsvd<sub>WMH</sub> also maintained consistently high Dice scores across these test datasets (mean DSC = 0.86 ± 0.08), and exhibited strong, stable correlations with periventricular, deep, and total WMH ground truth volumes (mean r = 0.99 ± 0.01). Additionally, segcsvd<sub>WMH</sub> was robust to low and moderate levels of simulated MRI spike noise artifacts and maintained strong performance across a range of binary segmentation thresholds and WMH burden levels. These findings suggest that segcsvd<sub>WMH</sub> may provide more accurate and robust WMH segmentation performance for heterogeneous clinical datasets characterized by varying degrees of CSVD severity.

Human Brain MappingVol. 45(18)
Western University (CA), Oslo University Hospital (NO), Sunnybrook Health Science Centre (CA), University Health Network (CA), Centre for Addiction and Mental Health (CA), University of Toronto (CA), Toronto Western Hospital (CA), Health Sciences Centre (CA), Baycrest Hospital (CA), Public Health Ontario (CA), University of Edinburgh (GB)
Canadian Institutes of Health Research
Openalex Percentile: Top 7%
Cerebrovascular and Carotid Artery Diseases
3.35
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