In this study, a real-time processing method for GRASE myelin water imaging is proposed by using an artificial neural network. Two different networks, one pairing multi-echo measurement with myelin water fraction and the other pairing multi-echo measurement with T2 distribution, were developed. Both networks took <1.5 sec for the whole brain processing (FOV = 240×180×112 mm3 and matrix = 160×120×28) with less than 5% error in white matter.
[Dataset]
To train and evaluate the ANNs, GRASE MWI data of 35 subjects (18 healthy controls (HC) and 17 MS patients) were utilized.1 The dataset was acquired with FOV = 240×180×112 mm3, matrix size = 160×120×28, and 32 echoes (TE1 = 10 ms; echo spacing of 10 ms). As a conventional method, the rNNLS method with stimulated echo correction was applied.4 For the network training, 12 slices of 28 slices covering a large white matter volume were selected. The total number of voxels was about 70,000 per subject.
[Artificial neural network I, II]
The ANN I was designed to generate a MWF from a T2 decay curve by training the network with the 32-echo measurement as the input and the MWF from the rNNLS as the label (Fig. 1). The network consisted of 4 layers: an input layer, 4 hidden layers (96, 128, 160, and 240 neurons each), and an output layer. A leaky ReLU was used as an non-linear activation function. The loss function was defined as the mean squared error between the network output and the label data.
The ANN II generates a T2 distribution from a T2 decay curve by training the network with the 32-echo measurement as the input and the T2 distribution from the rNNLS as the label (Fig. 1). The network structure was the same as the ANN I except for the output layer (120 neurons). To enforce nonnegative values in the T2 distribution, the negative values in the output were forced to zero.
[Evaluation]
As the first step, three different subject
compositions (14 HC only; 15 MS only; 7 HC and 8 MS combined) were trained to
test the effects of the subject type. Then, the training data size was
increased from 2 to 25 subjects to check the sufficient size for
generalization. Nine subjects (4 HC and 5 MS), not included in the training, were
used for this test. For the evaluation, the normalized root mean-squared error (NRMSE) was
calculated for the white matter mask including lesions.
Additionally, an ROI analysis for the five ROIs was performed. Lastly, the conventional MWI and the ANN II maps were compared
with three different thresholds (30, 40, and 50 ms). The processing time of both methods was measured on the same quad-core computer (Intel
i7-4790 CPU).
When the three subject compositions were compared, the training data with MS had smaller NRMSE (5.92%) than the data without MS (11.43%). For increasing number of training datasets, NRMSE saturated around 20 to 25 subjects. So the final networks were trained with 24 subjects (half HC and half MS). The remaining ten subjects (5 HC and 5 MS) were used for test.
The MWIs of the three methods with the difference maps in ×10 range are displayed in Fig. 2. The difference maps confirmed that the three results look similar. The average NRMSE was 4.67% in ANN I (HC:4.56%, MS:4.77%), and 4.79% in ANN II (HC:4.76%, MS:4.82%). The ROI analysis results (Table 1) show that the average MWFs in the five ROIs are not statistically different.
In Figure 3, the T2 distributions from ANN II and rNNLS are displayed, demonstrating the similarity in their shapes. Both methods revealed similar MWF maps even with the different thresholds, suggesting robustness of the ANN II in generating T2 distribution.
The processing time for the ANNs was <1.5 sec, which was shorter by 7200 times than that of the conventional method (>3 hours) on the same CPU.
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