Conventional Electrical Properties Tomography (EPT) suffers from reconstruction artifacts related to assumptions necessary for solving the equations analytically. To circumvent the necessity for these assumptions, in this study a deep learning approach is utilized to approximate the analytically unsolvable equations. For this purpose, a 3D convolutional neural network was trained on simulations and in-vivo data from healthy volunteers and cancer patients. Results demonstrate the potential of this method, as noise-free conductivity maps were obtained without anatomic apriori information in less than 1:30 min per reconstruction.
Electrical Properties Tomography (EPT) derives conductivity and permittivity of tissue from complex B1 maps, as obtainable with standard MR systems and sequences [1]. In conventional (Helmholtz-based) EPT (HHEPT), the analytical formulation of the reconstruction equation gives rise to the transceive phase assumption, artifacts along tissue boundaries [2] and severe noise amplification in the reconstructed electrical properties maps. This work tries to overcome these challenges, as no satisfying solution for them has been found yet.
Following up on recent success of machine learning methods in medical imaging [3], first investigations have proven their potential for EPT [4,5]. In this study, the analytically unsolvable equations underlying EPT are approximated with a convolutional neural network (DLEPT). Following the work on simulations of full electrical properties maps by [4], this work is dedicated to challenges in reconstructing in-vivo data, with focus on phase-based conductivity reconstruction.
This work utilizes 3D patches as in [5] to maximize the local information. Empirical investigations led to the choice of a U-net with two downsampling steps and patch size of 24x24x24. To eliminate physically irrelevant phase offsets, the mean phase value was subtracted from each phase-patch. Data were augmented by mirroring patches at each axis. The first dataset consists of realistic EM-simulations with realistic Gaussian noise added. Transceive phase simulations were performed on a 2mm grid in Sim4life after applying geometrical deformations to virtual population models Duke and Ella [6]. The resulting 15 models were placed into a quadrature head coil model at 128 MHz. By training a network only on deformations of Duke and validating it on original Duke (excluded from training) and Ella, the impact of geometrical variance is investigated. For validation on in-vivo data, the full simulation dataset is used for training.
In-vivo datasets were acquired using commercial 3T scanner (Philips Healthcare, Netherlands, equipped with quadrature RF head coil). After obtaining informed written consent according to local Institutional Review Boards, 14 patients (mean age 42 +/- 17 yrs ) with various brain lesions (see Tab.1) and 18 healthy volunteers (mean age 44 +/- 7 yrs) were scanned with a bSSFP sequence (TR/TE=3.4/1.7ms, voxel size=1x1x1mm, flip angle=25°, 2 averages, scan duration 3:40 minutes). Two networks were trained on a GPU (Nvidia GeForce GTX 1080 Ti) using separate in-vivo datasets (volunteers/patients), and a third network was trained on the combined dataset. A three-fold cross-validation was performed using data from both in-vivo datasets. For quantitative evaluations, the correlation between DLEPT reconstruction and HHEPT used as ground truth reference was calculated. HHEPT reconstructions were performed according to [7]. Throughout this work, all validation data were excluded from training.
Networks trained on simulations show excellent results for reconstruction of simulations, which however degrade with increasing head geometry differences from training data. This, along with the performance improvement when combining both datasets, demonstrates that lacking geometric variability in training datasets of the given size is a major cause of reconstruction errors for DLEPT.
Promising reconstructions from networks trained on in-vivo data demonstrate the possibility of overcoming artifacts present in in-vivo reconstructions from networks trained on simulations, by including artifacts in training. Decreasing accuracy for the network trained on volunteers validated on patients and vice-versa (Tab.2, Fig.2) indicates dataset specificity of these in-vivo artifacts.
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