TY - JOUR
T1 - Automatic spatial estimation of white matter hyperintensities evolution in brain MRI using disease evolution predictor deep neural networks
AU - Rachmadi, Muhammad Febrian
AU - Valdés-Hernández, Maria Del C
AU - Makin, Stephen
AU - Wardlaw, Joanna
AU - Komura, Taku
N1 - Funds from the Indonesia Endowment Fund for Education (LPDP), Ministry of Finance, Republic of Indonesia (MFR); Row Fogo Charitable Trust (Grant No. BRO-D.FID3668413)(MCVH); Wellcome Trust (patient recruitment, scanning, primary study Ref No. WT088134/Z/09/A); Fondation Leducq (Perivascular Spaces Transatlantic Network of Excellence); EU Horizon 2020 (SVDs@Target); and the MRC UK Dementia Research Institute at the University of Edinburgh (Wardlaw programme) are gratefully acknowledged. The Titan Xp used for this research was donated by the NVIDIA Corporation.
PY - 2020/7
Y1 - 2020/7
N2 - 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.
AB - 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.
KW - White matter hyperintensities (WMH)
KW - WMH Evolution
KW - Disease evolution predictor (DEP) models
KW - DEP Generative adversarial network (DEP-GAN)
KW - Small vessel disease (SVD)
KW - DEP U-Residual Network (DEP-UResNet)
KW - REGRESSION
KW - SMALL VESSEL DISEASE
KW - COGNITIVE CONSEQUENCES
KW - RISK-FACTORS
KW - VOLUME
KW - IMAGES
KW - DYNAMICS
KW - STROKE LESION SEGMENTATION
KW - PROGRESSION
KW - INSIGHTS
UR - http://europepmc.org/abstract/med/32428823
UR - http://www.scopus.com/inward/record.url?scp=85084653087&partnerID=8YFLogxK
U2 - 10.1016/j.media.2020.101712
DO - 10.1016/j.media.2020.101712
M3 - Article
C2 - 32428823
VL - 63
SP - 101712
JO - Medical image analysis
JF - Medical image analysis
M1 - 101712
ER -