There are increasing concerns over gadolinium-based-contrast-agents-administration(GBCA). A deep-learning (DL) method was developed to reduce the gadolinium dose in Contrast-Enhanced-MRI (CE-MRI). The proposed method includes an acquisition step(pre-contrast, 10% low-dose and full-dose CE-MRI with T1-weighted-IR-FSPGR), a pre-processing step and a deep learning model trained to predict full-dose CE-MRI from pre-contrast and low-dose images. Evaluated on a clinical neuro CE-MRI dataset (10 patients for training and another 20 patients for evaluation), both quantitative metrics and radiologists’ ratings showed the proposed method achieved improved synthesis, with better motion-artifact-suppression and NO significant differences in contrast-enhancement quality, compared with ground-truth full-dose CE-MRI. Thus, using the proposed Deep Learning method, GBCA can be reduced, by at-least-10-fold, while preserving image quality and diagnostic information.
Imaging Protocol: High-resolution 3D T1-weighted inversion-recovery prepped fast-spoiled-gradient-echo imaging (IR-FSPGR, T1 BRAVO, TR/TE/TI 9.5/3.8/400ms, matrix 512x512, FOV 240mm, thickness 1mm) was collected using 3T MRI scanners (GE Healthcare) on 30 patients ($$$48.5 \pm 19.2$$$ years, 17 males) receiving clinically indicated CE-MRI with clinical protocol. The protocol, as shown in Figure 1, includes following 3 sequences: high-resolution pre-contrast, post-contrast images with 10% low-dose and 100% full-dose of gadobenate dimeglumine (0.01 and 0.1 mmol/kg, respectively).
Pre-processing: The workflow of the method is shown in Figure 2. To remove systematic differences in non-enhancing regions and mitigate the variability of transmit and receive gains, co-registration and signal normalization was conducted based on average voxel value within masks.
Training Deep Learning model: The detailed model architecture (Figure 3) is an encoder-decoder convolutional neural network (CNN) with bypass connections and residual connections as U-Net[5,6]. The deep network implicitly learns the guided denoising of noisy contrast uptake in low-dose CE-MRI to synthesize full-dose CE-MRI from pre-contrast and low-dose CE-MRI. We trained the model using the first 10 cases and evaluated the trained model on the other 20 patients. In the training we used Mean-Absolute-Error cost function and the ADAM[7] method.
Assessment: The acquired low-dose, real full-dose, and the synthesized full-dose post-contrast images were compared quantitatively using peak-signal-to-noise-ratios (PSNR), structural-similarity-indexes (SSIM) and qualitative scores by 2 neuroradiologists.
Based on the quantitative similarity metrics, the proposed DL method yielded significant (p<0.001) improvements over the $$$10\%$$$ low-dose images, with over 5dB PSNR gains, $$$11.0\%$$$ SSIM increases and significant improvements in qualitative ratings.
From radiologists’ ratings (Figure 4), there were no significant differences (both p>0.05) in image quality or contrast enhancement between the synthesized and acquired full-dose images. In addition, significantly better (p<0.05) artifact suppression was noted.
Figure 5 shows a visual comparison between pre-dose MRI, 10% low-dose CE-MRI, reference full-dose CE-MRI and the synthesized CE-MRI using the proposed method. The synthesized image demonstrates high image quality, preserved contrast enhancements and less motion artifacts.
The proposed deep learning based method enables a 90% reduction of Gadolinium dose, which significantly reduces risks for patients. It can also be used to enhance image quality for cases where low contrast dose has already been administrated for reasons (e.g. pediatric imaging).
The proposed technique can be further improved by using more controlled experiment designs to mitigate the effects of different imaging settings and timing. In addition, further performance improvement can be achieved with 3D models and different cost functions[8]. It is reasonable to explore further reduction of Gadolinium dosage above the 90% reduction, by incorporating improved DL algorithms, using larger training datasets with more variable pathologies as well as other complimentary information from multi-contrast MRI and clinical history.