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Dairong Cao

Publications and source records attributed to Dairong Cao.

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FlexDTI: Flexible diffusion gradient encoding scheme-based highly efficient diffusion tensor imaging using deep learning

Objective: Most deep neural network-based diffusion tensor imaging methods require the diffusion gradients' number and directions in the data to be reconstructed to match those in the training data. This work aims to develop and evaluate a novel dynamic-convolution-based method called FlexDTI for highly efficient diffusion tensor reconstruction with flexible diffusion encoding gradient scheme. Approach: FlexDTI was developed to achieve high-quality DTI parametric mapping with flexible number and directions of diffusion encoding gradients. The method used dynamic convolution kernels to embed diffusion gradient direction information into feature maps of the corresponding diffusion signal. Furthermore, it realized the generalization of a flexible number of diffusion gradient directions by setting the maximum number of input channels of the network. The network was trained and tested using datasets from the Human Connectome Project and local hospitals. Results from FlexDTI and other advanced tensor parameter estimation methods were compared. Main results: Compared to other methods, FlexDTI successfully achieves high-quality diffusion tensor-derived parameters even if the number and directions of diffusion encoding gradients change. It reduces normalized root mean squared error (NRMSE) by about 50% on fractional anisotropy (FA) and 15% on mean diffusivity (MD), compared with the state-of-the-art deep learning method with flexible diffusion encoding gradient scheme. Significance: FlexDTI can well learn diffusion gradient direction information to achieve generalized DTI reconstruction with flexible diffusion gradient scheme. Both flexibility and reconstruction quality can be taken into account in this network.

eess.IV

DSC-MRI derived relative CBV maps synthesized from IVIM-MRI data:Application in glioma IDH mutation status identification

Objectives:To develop a framework for obtaining dynamic susceptibility contrast magnetic resonance imaging (DSC-MRI) derived relative cerebral blood volume (rCBV) maps without gadolinium-based contrast agent (GBCA) injection. Methods:This retrospective study included 146 patients (124 IDH wildtype; 22 IDH mutation) diagnosed with glioma. The DSC-MRI-derived rCBV maps were synthesized from intravoxel incoherent motion (IVIM) MRI data by the deep neural network trained only with IDH wildtype data due to thedata imbalance. Linear regression analysis, Pearson correlation coefficient, and Bland-Altman analysis, were done to evaluate the consistency between real and synthetic rCBV maps. The generalizability of the proposed framework was evaluated with IDH mutation data. IDH mutation status identification ability of real and synthetic rCBV maps was analyzed and compared using ROC analysis and the DeLong test. Results:Linear regression analysis shows a linear relationship between real and synthetic rCBV maps with a relatively high Pearson correlation coefficient (IDH wildtype: Pearson P = 0.7536; IDH mutation: Pearson P = 0.8933). Bland-Altman analysis between real and synthetic rCBV maps shows that almost all the data distribute within the 95% limits of agreement (IDH wildtype: 19 of 20 [95%]; IDH mutation: 19 of 20 [95%]). ROC analysis and the DeLong test show that the IDH mutation status identification abilities of real (AUC = 0.8375) and synthetic rCBV (AUC = 0.8325) are comparable and show no significant difference (P = 0.9075). Conclusions:It is feasible to obtain DSC-MRI-derived rCBV maps without the injection of GBCA. The synthetic rCBV map shows high consistency with real one.

physics.med-ph