Abstract

Diffusion tensor imaging (DTI) is currently the unique imaging technique that can detect the structure of in-vivo human myocardium without invasivity and radiation. However, it is particularly sensitive to motions, especially respiratory motion that results in serious signal loss in diffusion-weighted (DW) images. This makes it impossible to accurately measure cardiac microscopic structural properties. To cope with such problem, this paper proposes an unsupervised dense-encoder-fusion-decoder network (DEFD-net) to compensate for signal loss in cardiac DW images, which allows investigating in-vivo myocardium structure more accurately. The DEFD-net consists of three modules, namely dense-encoder, fusion module and decoder module. The dense-encoder and decoder are trained firstly with DW images acquired at different trigger delays in an unsupervised manner for extracting local and global features. A fusion strategy is then designed to fuse the extracted features. Finally, the well-trained decoder is used to reconstruct the fused DW image from the fused features. To validate the superiority of the proposed method, comparison with existing methods such as PCAMIP, WIF and U2Fusion is performed on both simulated and acquired datasets. The experimental results showed that the proposed method effectively compensates for motion-induced signal loss in DW images, thus leading to much better DW image quality with respect to existing methods. Moreover, the subsequently derived myocardium fiber structure is more regular.

Highlights

  • According to the latest WHO (World Health Organization) report, more than 11.7 million people died of cardiovascular disease each year, and 80% of cardiovascular deaths were caused by myocardial infarction and stroke [1]

  • The simulated cardiac diffusion weighted (DW) images were obtained with the method proposed by Wang et al [31], in which 14 slices of CCBM heart were selected for modeling and simulation

  • We proposed a DEFD-net network for investigating in-vivo cardiac Diffusion Tensor Imaging (DTI) properties from DW images acquired at the end of diastole phase under free-breathing with multiple trigger delays

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Summary

Introduction

According to the latest WHO (World Health Organization) report, more than 11.7 million people died of cardiovascular disease each year, and 80% of cardiovascular deaths were caused by myocardial infarction and stroke [1]. The cardiovascular diseases are closely related to the structure of myocardial fibers. Investigating the structure of myocardial fibers can potentially make early diagnosis of cardiovascular diseases become possible and have important significance in explaining the causes of cardiovascular diseases [2],[3]. Diffusion Tensor Imaging (DTI) is currently the unique imaging technique that can detect non-invasively the myocardial structure of in-vivo human heart without radiation [4]–[7]. It estimates myocardial fiber orientations by measuring the diffusion displacement distribution of water molecules in fibrous tissue from diffusion weighted (DW) images along different diffusion gradient directions. Diffusion metrics, including fractional anisotropy (FA), mean diffusivity (MD) and helix angle (HA) are often calculated from DTI for describing the myocardium structure [6]–[8]

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