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Register a new userCombining Deep Learning and 3D Contrast Source Inversion in MR-based Electrical Properties Tomography
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Magnetic resonance-electrical properties tomography (MR-EPT) is a technique used to estimate the conductivity and permittivity of tissues from MR measurements of the transmit magnetic field. Different reconstruction methods are available, however all these methods present several limitations which hamper the clinical applicability. Standard Helmholtz based MR-EPT methods are severely affected by noise. Iterative reconstruction methods such as contrast source inversion-EPT (CSI-EPT) are typically time consuming and are dependent on their initialization. Deep learning (DL) based methods require a large amount of training data before sufficient generalization can be achieved. Here, we investigate the benefits achievable using a hybrid approach, i.e. using MR-EPT or DL-EPT as initialization guesses for standard 3D CSI-EPT. Using realistic electromagnetic simulations at 3 T and 7 T, the accuracy and precision of hybrid CSI reconstructions are compared to standard 3D CSI-EPT reconstructions. Our results indicate that a hybrid method consisting of an initial DL-EPT reconstruction followed by a 3D CSI-EPT reconstruction would be beneficial. DL-EPT combined with standard 3D CSI-EPT exploits the power of data driven DL-based EPT reconstructions while the subsequent CSI-EPT facilitates a better generalization by providing data consistency.
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Magnetic Resonance Fingerprinting (MRF) enables the simultaneous quantification of multiple properties of biological tissues. It relies on a pseudo-random acquisition and the matching of acquired signal evolutions to a precomputed dictionary. However, the dictionary is not scalable to higher-parametric spaces, limiting MRF to the simultaneous mapping of only a small number of parameters (proton density, T1 and T2 in general). Inspired by diffusion-weighted SSFP imaging, we present a proof-of-concept of a novel MRF sequence with embedded diffusion-encoding gradients along all three axes to efficiently encode orientational diffusion and T1 and T2 relaxation. We take advantage of a convolutional neural network (CNN) to reconstruct multiple quantitative maps from this single, highly undersampled acquisition. We bypass expensive dictionary matching by learning the implicit physical relationships between the spatiotemporal MRF data and the T1, T2 and diffusion tensor parameters. The predicted parameter maps and the derived scalar diffusion metrics agree well with state-of-the-art reference protocols. Orientational diffusion information is captured as seen from the estimated primary diffusion directions. In addition to this, the joint acquisition and reconstruction framework proves capable of preserving tissue abnormalities in multiple sclerosis lesions.
The susceptibility-based positive contrast MR technique was applied to estimate arbitrary magnetic susceptibility distributions of the metallic devices using a kernel deconvolution algorithm with a regularized L-1 minimization.Previously, the first-order primal-dual (PD) algorithm could provide a faster reconstruction time to solve the L-1 minimization, compared with other methods. Here, we propose to accelerate the PD algorithm of the positive contrast image using the multi-core multi-thread feature of graphics processor units (GPUs). The some experimental results showed that the GPU-based PD algorithm could achieve comparable accuracy of the metallic interventional devices in positive contrast imaging with less computational time. And the GPU-based PD approach was 4~15 times faster than the previous CPU-based scheme.
The MR-Linac is a combination of an MR-scanner and radiotherapy linear accelerator (Linac) which holds the promise to increase the precision of radiotherapy treatments with MR-guided radiotherapy by monitoring motion during radiotherapy with MRI, and adjusting the radiotherapy plan accordingly. Optimal MR-guidance for respiratory motion during radiotherapy requires MR-based 3D motion estimation with a latency of 200-500 ms. Currently this is still challenging since typical methods rely on MR-images, and are therefore limited by the 3D MR-imaging latency. In this work, we present a method to perform non-rigid 3D respiratory motion estimation with 170 ms latency, including both acquisition and reconstruction. The proposed method called real-time low-rank MR-MOTUS reconstructs motion-fields directly from k-space data, and leverages an explicit low-rank decomposition of motion-fields to split the large scale 3D+t motion-field reconstruction problem posed in our previous work into two parts: (I) a medium-scale offline preparation phase and (II) a small-scale online inference phase which exploits the results of the offline phase for real-time computations. The method was validated on free-breathing data of five volunteers, acquired with a 1.5T Elekta Unity MR-Linac. Results show that the reconstructed 3D motion-field are anatomically plausible, highly correlated with a self-navigation motion surrogate (R = 0.975 +/- 0.0110), and can be reconstructed with a total latency of 170 ms that is sufficient for real-time MR-guided abdominal radiotherapy.
Purpose: To study the accuracy of motion information extracted from beat-to-beat 3D image-based navigators (3D iNAVs) collected using a variable-density cones trajectory with different combinations of spatial resolutions and scan acceleration factors. Methods: Fully sampled, breath-held 4.4 mm 3D iNAV datasets for six respiratory phases are acquired in a volunteer. Ground truth translational and nonrigid motion information is derived from these datasets. Subsequently, the motion estimates from synthesized undersampled 3D iNAVs with isotropic spatial resolutions of 4.4 mm (acceleration factor = 10.9), 5.4 mm (acceleration factor = 7.2), 6.4 mm (acceleration factor = 4.2), and 7.8 mm (acceleration factor = 2.9) are assessed against the ground truth information. The undersampled 3D iNAV configuration with the highest accuracy motion estimates in simulation is then compared with the originally proposed 4.4 mm undersampled 3D iNAV in six volunteer studies. Results: The simulations indicate that for navigators beyond certain scan acceleration factors, the accuracy of motion estimates is compromised due to errors from residual aliasing and blurring/smoothening effects following compressed sensing reconstruction. The 6.4 mm 3D iNAV achieves an acceptable spatial resolution with a small acceleration factor, resulting in the highest accuracy motion information among all assessed undersampled 3D iNAVs. Reader scores for six volunteer studies demonstrate superior coronary vessel sharpness when applying an autofocusing nonrigid correction technique using the 6.4 mm 3D iNAVs in place of 4.4 mm 3D iNAVs. Conclusion: Undersampled 6.4 mm 3D iNAVs enable motion tracking with improved accuracy relative to previously proposed undersampled 4.4 mm 3D iNAVs.
Objectives: Precise segmentation of total extraocular muscles (EOM) and optic nerve (ON) is essential to assess anatomical development and progression of thyroid-associated ophthalmopathy (TAO). We aim to develop a semantic segmentation method based on deep learning to extract the total EOM and ON from orbital CT images in patients with suspected TAO. Materials and Methods: A total of 7,879 images obtained from 97 subjects who underwent orbit CT scans due to suspected TAO were enrolled in this study. Eighty-eight patients were randomly selected into the training/validation dataset, and the rest were put into the test dataset. Contours of the total EOM and ON in all the patients were manually delineated by experienced radiologists as the ground truth. A three-dimensional (3D) end-to-end fully convolutional neural network called semantic V-net (SV-net) was developed for our segmentation task. Intersection over Union (IoU) was measured to evaluate the accuracy of the segmentation results, and Pearson correlation analysis was used to evaluate the volumes measured from our segmentation results against those from the ground truth. Results: Our model in the test dataset achieved an overall IoU of 0.8207; the IoU was 0.7599 for the superior rectus muscle, 0.8183 for the lateral rectus muscle, 0.8481 for the medial rectus muscle, 0.8436 for the inferior rectus muscle and 0.8337 for the optic nerve. The volumes measured from our segmentation results agreed well with those from the ground truth (all R>0.98, P<0.0001). Conclusion: The qualitative and quantitative evaluations demonstrate excellent performance of our method in automatically extracting the total EOM and ON and measuring their volumes in orbital CT images. There is a great promise for clinical application to assess these anatomical structures for the diagnosis and prognosis of TAO.
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