Laifa Ma1, Weili Lin1, He Zhang2, and Gang Li1
1University of North Carolina at Chapel Hill, Chapel Hill, NC, United States, 2Fudan University, Shanghai, China
Synopsis
Keywords: Image Reconstruction, Brain
Motivation: The fetal brain MRI 3D volume is critical for development assessment. However, the inevitable fetal motion during MRI acquisition makes it challenging to reconstruct a high-quality fetal brain 3D volume from multiple stacks.
Goal(s): Herein, we propose a novel deep learning method for automated fetal brain MRI 3D volume reconstruction.
Approach: Firstly, a multi-scale feature fusion model is proposed to solve arbitrary motion correction. Secondly, an initial 3D volume is estimated by point spread function. Next, the proposed residual-based model is used to improve the quality of the initial 3D volume.
Results: The results demonstrate that the proposed method is effective and efficient.
Impact: The
proposed end-to-end method based on deep learning can solve arbitrary motion
correction of 2D slices and reconstruct high-resolution fetal brain MRI 3D
volumes effectively and efficiently.
Introduction
Fetal brain magnetic resonance imaging can provide more detailed and accurate 3D information of brain morphology, making it particularly critical for fetal brain malformation diagnosis and development assessment [1]. However, the inevitable fetal motion and maternal breathing during MRI acquisition can result in loss of structural continuity and corrupted volumetric information. Although fast imaging techniques can overcome the in-plane motion of individual 2D slices [2], the motion between slices still exists. Therefore, there is an urgent need to reconstruct high-quality fetal brain 3D volumes from multiple motion-corrupted 2D slices. Although the traditional iterative motion correction and reconstruction approaches have proven effective, they have two major limitations: 1) limited to capturing relatively small motion; and 2) time-consuming. Herein, we propose a novel end-to-end learning-based fetal brain MRI 3D volume reconstruction method. The main contributions are as follows. 1) A multi-scale feature fusion model is proposed to correct arbitrary motion of 2D slices. 2) A residual-based encoder-decoder model with a specifically designed perceptual loss reconstructs the high-resolution fetal brain MRI 3D volume with anatomically realistic details further by using an adversarial loss.Methods and Materials
We propose an end-to-end highly efficient fetal brain MRI 3D
volume reconstruction method based on deep learning, as shown in Fig. 1. It consists
of three steps: 1) motion estimation and correction, 2)
initial volume reconstruction, and 3) high-quality high-resolution volume
reconstruction.
First, a multi-scale feature fusion model is proposed to predict
motions of fetal brain MRI 2D slices. It includes a bottom-up path, a top-down
path, and lateral connections, as shown in Fig. 2. The bottom-up path is the
feature extraction backbone of the model, which is composed of basic residual
blocks to generate feature maps at four different scales. The top-down path
generates higher resolution features through up-sampling. Then, the feature
maps of the bottom-up and top-down paths are fused by lateral connections. The model
can capture both fine-grained details and global context information at
different scales, thus enabling the model to handle different slices with
different appearances. Similar to SVRnet [3], anchor points are used
to define motion parameters, and L1 loss is used to train the model.
Then, according to the predicted motion parameters, an initial
3D volume is estimated by point spread function. To improve the initial 3D
volume quality, we develop a residual-based encoder-decoder model, which can
learn an enriched set of textural and structural features, as shown in Fig.
3(a). To optimize the model for achieving better performance, we design a perceptual
loss, as shown in Fig. 3(b), which measures the difference between two 3D
volumes in terms of the feature map similarity, rather than pixel-wise
differences to preserve more textural and structural details. To produce
anatomically more realistic details on the reconstructed 3D volume, the
adversarial loss is introduced as in WGAN. A simple discriminator network is
proposed to calculate the Wasserstein distance between the ground truth 3D
volume and the reconstructed 3D volume, as shown in Fig. 3(b).
We developed the model based on 279 T2-weighted fetal brain MRI volumes between 21 and 38 weeks of gestational age. For training purpose, these fetal volumes were reconstructed using NiftyMIC[4] with 0.8 mm isotropic resolution. The datasets applied to simulate the fetal brain motion were divided into training (194), validation (30), and test (55) sets. The models were implemented with Pytorch, and trained on NVIDIA TITAN Xp GPU using Adam optimizer. The fetal motion simulation method is similar to [4].Results
The standard metrics Structural Similarity (SSIM) and Peak
Signal-to-Noise Ratio (PSNR) are used to evaluate the performance of methods. The
run time is used to evaluate efficiency. We adopted NiftyMIC [5] and
SVRTK [6] as baselines for comparison. In terms of PSNR, our method
improves by 7.14 and 2.96 compared to SVRTK and NiftyMIC, respectively.
According to SSIM, our method improves by 0.194 and 0.237, respectively. Compared
with these methods, the proposed method achieved the speedup of 167.9 and 21.8
times, respectively. Fig. 4 shows the representative reconstruction results
obtained by different methods.Conclusions
In this work, an end-to-end, highly efficient method based on
deep learning is proposed to reconstruct fetal brain MRI 3D volume. The multi-scale
feature fusion model can solve arbitrary motion correction of 2D slices. Our designed
residual-based encoder-decoder model can learn an enriched set of features to
reconstruct high-resolution fetal brain MRI 3D volume. The results demonstrate
the proposed method is able to reconstruct high-resolution 3D volumes with high
efficiency and accuracy. Acknowledgements
This work was supported in part by NIH grants (MH116225, MH117943 and MH123202 to G.L.).References
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