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Updated: May 28, 2026

Evaluation of the Cognitive Performance of Hypertensive Patients with Silent Cerebrovascular Lesions
Published on: April 23, 2021
Complexity of MRI white matter hyperintensity assessments in relation to cognition in aging and dementia from the
Fu-qiang Gao1, Richard H Swartz, Philip Scheltens
1LC Campbell Cognitive Neurology Research Unit, Heart and Stroke Foundation Centre for Stroke Recovery, University of Toronto, Toronto, ON, Canada. fgao@sri.utoronto.ca
Purpose:
Quantification methods for white matter hyperintensities (WMH) on Magnetic Resonance Imaging are heterogeneous, deterring their application. This study compared three WMH rating scales, varying in complexity, and a volumetric method, to evaluate trade-offs between complexity and clinical utility in differentiating dementia subgroups and in correlating with cognition.
Methods:
WMH were rated using the Fazekas, Age-Related White Matter Changes (ARWMC) and Scheltens scales, and segmented by computational volumetry in 108 patients with Alzheimer's Disease (AD), 23 with Mild Cognitive Impairment (MCI) and 34 normal controls (NC). Global and hippocampal atrophy, age and education, were accounted for in correlations of WMH with cognitive domains.
Results:
Intra- and inter-rater reliability were high (intraclass correlation coefficients = 0.88-0.97) across rating scales. WMH scores of all scales were highly correlated with volumes (Spearman r = 0.78-0.90, Ps < 0.001), as well as with each other (Spearman r = 0.86-0.91, Ps < 0.001). The Fazekas scale showed significant separation between AD, MCI and NC using non-parametric analysis, while the ARWMC and Scheltens' scales, and WMH volumes demonstrated significant correlations (standardized β = -0.19 to -0.24, Ps < 0.05) with cognitive domain scores using multivariate regression analysis, controlling for age, education, global and hippocampal atrophy in patients with AD.
Conclusions:
This study suggests that the degree of complexity of WMH rating scales did not affect validation against WMH volumes, but did vary in validation against cognition. The simplest scale performed best in separating cognitive subgroups, but the more complex scales and quantification correlated better with cognitive measures, especially executive function. Hence the best choice of scale depends on the particular application.
Insights
Comparing white matter hyperintensities (WMH) scales for dementia diagnosis, this study found simpler scales better for subgroup separation, while complex scales and volumetry correlated more with cognitive function, especially executive function.
Area of Science:
- Neuroimaging
- Neurology
- Radiology
Background:
- White matter hyperintensities (WMH) quantification methods on MRI are inconsistent, limiting clinical application.
- Standardized WMH assessment is crucial for understanding neurodegenerative diseases.
Purpose of the Study:
- To compare the clinical utility of three WMH rating scales (Fazekas, ARWMC, Scheltens) and a volumetric method.
- To evaluate the trade-offs between scale complexity and their ability to differentiate dementia subgroups and correlate with cognition.
Main Methods:
- WMH were rated using Fazekas, ARWMC, and Scheltens scales and computationally segmented for volume in 108 Alzheimer's Disease (AD), 23 Mild Cognitive Impairment (MCI), and 34 normal control (NC) patients.
- Correlations with cognitive domains controlled for age, education, and global/hippocampal atrophy.
Main Results:
- High intra- and inter-rater reliability (ICC=0.88-0.97) for all rating scales.
- WMH scores strongly correlated with volumes (r=0.78-0.90) and with each other (r=0.86-0.91).
- Fazekas scale separated AD, MCI, and NC; ARWMC, Scheltens, and volumes correlated with cognition (β=-0.19 to -0.24).
Conclusions:
- WMH scale complexity did not impact validation against volumes but affected cognitive correlation.
- Simpler scales excelled at subgroup separation, while complex scales/quantification better predicted cognitive measures, particularly executive function.
- The optimal WMH assessment method depends on the specific clinical or research application.
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