Abstract

Previous studies have indicated that white matter hyperintensities (WMH), the main radiological feature of small vessel disease, may evolve (i.e., shrink, grow) or stay stable over a period of time. Predicting these changes are challenging because it involves some unknown clinical risk factors that leads to a non-deterministic prediction task. In this study, we propose a deep learning model to predict the evolution of WMH from baseline to follow-up (i.e., 1-year later), namely "Disease Evolution Predictor" (DEP) model, which can be adjusted to become a non-deterministic model. The DEP model receives a baseline image as input and produces a map called "Disease Evolution Map" (DEM), which represents the evolution of WMH from baseline to follow-up. Two DEP models are proposed, namely DEP-UResNet and DEP-GAN, which are representatives of the supervised (i.e., need expert-generated manual labels to generate the output) and unsupervised (i.e., do not require manual labels produced by experts) deep learning algorithms respectively. To simulate the non-deterministic and unknown parameters involved in WMH evolution, we modulate a Gaussian noise array to the DEP model as auxiliary input. This forces the DEP model to imitate a wider spectrum of alternatives in the prediction results. The alternatives of using other types of auxiliary input instead, such as baseline WMH and stroke lesion loads are also proposed and tested. Based on our experiments, the fully supervised machine learning scheme DEP-UResNet regularly performed better than the DEP-GAN which works in principle without using any expert-generated label (i.e., unsupervised). However, a semi-supervised DEP-GAN model, which uses probability maps produced by a supervised segmentation method in the learning process, yielded similar performances to the DEP-UResNet and performed best in the clinical evaluation. Furthermore, an ablation study showed that an auxiliary input, especially the Gaussian noise, improved the performance of DEP models compared to DEP models that lacked the auxiliary input regardless of the model's architecture. To the best of our knowledge, this is the first extensive study on modelling WMH evolution using deep learning algorithms, which deals with the non-deterministic nature of WMH evolution.

Highlights

  • White matter hyperintensities (WMH), together with lacunar ischaemic strokes, lacunes, cerebral microbleeds, and perivascular∗∗ Corresponding author at: Centre for Clinical Brain Sciences, Chancellor’s Building, Edinburgh BioQuarter, 49 Little France Crescent, Edinburgh EH16 4SB, United Kingdom.spaces, are the main neuroradiological features of cerebral small vessel disease (SVD) (Wardlaw et al, 2013)

  • We investigated three different levels of human supervision in predicting WMH evolution: 1) supervised Disease Evolution Predictor” (DEP)-U-Residual Network (UResNet) using expert-generated manual labels, 2) unsupervised DEPGAN using Irregularity map (IM) produced by an unsupervised segmentation method of LOTS-IM (Rachmadi et al, 2019), and 3) semisupervised DEP-Generative Adversarial Network (GAN) using Probability map (PM) produced by a supervised segmentation method of UResNet

  • We proposed a training scheme to predict the evolution of WMH using deep learning algorithms, namely Disease Evolution Predictor (DEP) model

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Summary

Introduction

White matter hyperintensities (WMH), together with lacunar ischaemic strokes, lacunes, cerebral microbleeds, and perivascular∗∗ Corresponding author at: Centre for Clinical Brain Sciences, Chancellor’s Building, Edinburgh BioQuarter, 49 Little France Crescent, Edinburgh EH16 4SB, United Kingdom.spaces, are the main neuroradiological features of cerebral small vessel disease (SVD) (Wardlaw et al, 2013). White matter hyperintensities (WMH), together with lacunar ischaemic strokes, lacunes, cerebral microbleeds, and perivascular. WMH can be observed in T2-weighted and T2-fluid attenuated inversion recovery (T2-FLAIR) brain magnetic resonance images (MRI), sharing similar neuroradiological characteristics as the lacunar ischaemic infarcts and enlarged perivascular spaces WMH have been associated with stroke, ageing, and dementia progression (Prins and Scheltens, 2015; Wardlaw et al, 2017a). Recent studies have shown that WMH may decrease (i.e., shrink/regress), stay unchanged (i.e., stable), or increase (i.e., grow/progress) over a period of time (Ramirez et al, 2016). Variations in the WMH burden over time have been associated with patients’ comorbidities and clinical outcome (Chappell et al, 2017; Wardlaw et al, 2017b). We refer to theses changes as “evolution of WMH”

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