Validation of a Regression Technique for Segmentation of White Matter Hyperintensities in Alzheimer’s Disease

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Abstract
Segmentation and volumetric quantification of white matter hyperintensities (WMHs) is essential in assessment and monitoring of the vascular burden in aging and Alzheimer's disease (AD), especially when considering their effect on cognition. Manually segmenting WMHs in large cohorts is technically unfeasible due to time and accuracy concerns. Automated tools that can detect WMHs robustly and with high accuracy are needed. Here, we present and validate a fully automatic technique for segmentation and volumetric quantification of WMHs in aging and AD. The proposed technique combines intensity and location features from multiple magnetic resonance imaging contrasts and manually labeled training data with a linear classifier to perform fast and robust segmentations. It provides both a continuous subject specific WMH map reflecting different levels of tissue damage and binary segmentations. The method was used to detect WMHs in 80 elderly/AD brains (ADC data set) as well as 40 healthy subjects at risk of AD (PREVENT-AD data set). Robustness across different scanners was validated using ten subjects from ADNI2/GO study. Voxel-wise and volumetric agreements were evaluated using Dice similarity index (SI) and intra-class correlation (ICC), yielding ICC = 0.96, SI = 0.62±0.16 for ADC data set and ICC = 0.78, SI = 0.51 ± 0.15 for PREVENT-AD data set. The proposed method was robust in the independent sample yielding SI = 0.64 ± 0.17 with ICC = 0.93 for ADNI2/GO subjects. The proposed method provides fast, accurate, and robust segmentations on previously unseen data from different models of scanners, making it ideal to study WMHs in large scale multi-site studies.
Funding Information
  • Canadian Institutes of Health Research (MOP-111169)
  • National Institutes of Health Grant (U01 AG024904)
  • les Fonds de Research Santé Québec Pfizer Innovation
  • Center for Scientific Review (K01 AG030514, P30AG010129)
  • NSERC CREATE (4140438 - 2012)

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