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Multi-Modal MRI Reconstruction with Spatial Alignment Network

2021-08-12 08:46:35
Kai Xuan, Lei Xiang, Xiaoqian Huang, Lichi Zhang, Shu Liao, Dinggang Shen, Qian Wang

Abstract

In clinical practice, magnetic resonance imaging (MRI) with multiple contrasts is usually acquired in a single study to assess different properties of the same region of interest in human body. The whole acquisition process can be accelerated by having one or more modalities under-sampled in the k-space. Recent researches demonstrate that, considering the redundancy between different contrasts or modalities, a target MRI modality under-sampled in the k-space can be better reconstructed with the helps from a fully-sampled sequence (i.e., the reference modality). It implies that, in the same study of the same subject, multiple sequences can be utilized together toward the purpose of highly efficient multi-modal reconstruction. However, we find that multi-modal reconstruction can be negatively affected by subtle spatial misalignment between different sequences, which is actually common in clinical practice. In this paper, we integrate the spatial alignment network with reconstruction, to improve the quality of the reconstructed target modality. Specifically, the spatial alignment network estimates the spatial misalignment between the fully-sampled reference and the under-sampled target images, and warps the reference image accordingly. Then, the aligned fully-sampled reference image joins the under-sampled target image in the reconstruction network, to produce the high-quality target image. Considering the contrast difference between the target and the reference, we particularly design the cross-modality-synthesis-based registration loss, in combination with the reconstruction loss, to jointly train the spatial alignment network and the reconstruction network. Our experiments on both clinical MRI and multi-coil k-space raw data demonstrate the superiority and robustness of our spatial alignment network. Code is publicly available at this https URL.

Abstract (translated)

URL

https://arxiv.org/abs/2108.05603

PDF

https://arxiv.org/pdf/2108.05603.pdf


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