82 research outputs found

    DRIMET: Deep Registration for 3D Incompressible Motion Estimation in Tagged-MRI with Application to the Tongue

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    Tagged magnetic resonance imaging (MRI) has been used for decades to observe and quantify the detailed motion of deforming tissue. However, this technique faces several challenges such as tag fading, large motion, long computation times, and difficulties in obtaining diffeomorphic incompressible flow fields. To address these issues, this paper presents a novel unsupervised phase-based 3D motion estimation technique for tagged MRI. We introduce two key innovations. First, we apply a sinusoidal transformation to the harmonic phase input, which enables end-to-end training and avoids the need for phase interpolation. Second, we propose a Jacobian determinant-based learning objective to encourage incompressible flow fields for deforming biological tissues. Our method efficiently estimates 3D motion fields that are accurate, dense, and approximately diffeomorphic and incompressible. The efficacy of the method is assessed using human tongue motion during speech, and includes both healthy controls and patients that have undergone glossectomy. We show that the method outperforms existing approaches, and also exhibits improvements in speed, robustness to tag fading, and large tongue motion.Comment: Accepted to MIDL 2023 (full paper

    WarpPINN: Cine-MR image registration with physics-informed neural networks

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    Heart failure is typically diagnosed with a global function assessment, such as ejection fraction. However, these metrics have low discriminate power, failing to distinguish different types of this disease. Quantifying local deformations in the form of cardiac strain can provide helpful information, but it remains a challenge. In this work, we introduce WarpPINN, a physics-informed neural network to perform image registration to obtain local metrics of the heart deformation. We apply this method to cine magnetic resonance images to estimate the motion during the cardiac cycle. We inform our neural network of near-incompressibility of cardiac tissue by penalizing the jacobian of the deformation field. The loss function has two components: an intensity-based similarity term between the reference and the warped template images, and a regularizer that represents the hyperelastic behavior of the tissue. The architecture of the neural network allows us to easily compute the strain via automatic differentiation to assess cardiac activity. We use Fourier feature mappings to overcome the spectral bias of neural networks, allowing us to capture discontinuities in the strain field. We test our algorithm on a synthetic example and on a cine-MRI benchmark of 15 healthy volunteers. We outperform current methodologies both landmark tracking and strain estimation. We expect that WarpPINN will enable more precise diagnostics of heart failure based on local deformation information. Source code is available at https://github.com/fsahli/WarpPINN.Comment: 18 pages, 10 figure

    Three Dimensional Tissue Motion Analysis from Tagged Magnetic Resonance Imaging

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    Motion estimation of soft tissues during organ deformation has been an important topic in medical imaging studies. Its application involves a variety of internal and external organs including the heart, the lung, the brain, and the tongue. Tagged magnetic resonance imaging has been used for decades to observe and quantify motion and strain of deforming tissues. It places temporary noninvasive markers—so called "tags"—in the tissue of interest that deform together with the tissue during motion, producing images that carry motion information in the deformed tagged patterns. These images can later be processed using phase-extraction algorithms to achieve motion estimation and strain computation. In this dissertation, we study three-dimensional (3D) motion estimation and analysis using tagged magnetic resonance images with applications focused on speech studies and traumatic brain injury modeling. Novel algorithms are developed to assist tagged motion analysis. Firstly, a pipeline of methods—TMAP—is proposed to compute 3D motion from tagged and cine images of the tongue during speech. TMAP produces an estimation of motion along with a multi-subject analysis of motion pattern differences between healthy control subjects and post-glossectomy patients. Secondly, an enhanced 3D motion estimation algorithm—E-IDEA—is proposed. E-IDEA tackles the incompressible motion both on the internal tissue region and the tissue boundaries, reducing the boundary errors and yielding a motion estimate that is more accurate overall. Thirdly, a novel 3D motion estimation algorithm—PVIRA—is developed. Based on image registration and tracking, PVIRA is a faster and more robust method that performs phase extraction in a novel way. Lastly, a method to reveal muscles' activity using strain in the line of action of muscle fiber directions is presented. It is a first step toward relating motion production with individual muscles and provides a new tool for future clinical and scientific use

    Cardiac motion estimation from medical images: a regularisation framework applied on pairwise image registration displacement fields

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    Accurate cardiac motion estimation from medical images such as ultrasound is important for clinical evaluation. We present a novel regularisation layer for cardiac motion estimation that will be applied after image registration and demonstrate its effectiveness. The regularisation utilises a spatio-temporal model of motion, b-splines of Fourier, to fit to displacement fields from pairwise image registration. In the process, it enforces spatial and temporal smoothness and consistency, cyclic nature of cardiac motion, and better adherence to the stroke volume of the heart. Flexibility is further given for inclusion of any set of registration displacement fields. The approach gave high accuracy. When applied to human adult Ultrasound data from a Cardiac Motion Analysis Challenge (CMAC), the proposed method is found to have 10% lower tracking error over CMAC participants. Satisfactory cardiac motion estimation is also demonstrated on other data sets, including human fetal echocardiography, chick embryonic heart ultrasound images, and zebrafish embryonic microscope images, with the average Dice coefficient between estimation motion and manual segmentation at 0.82–0.87. The approach of performing regularisation as an add-on layer after the completion of image registration is thus a viable option for cardiac motion estimation that can still have good accuracy. Since motion estimation algorithms are complex, dividing up regularisation and registration can simplify the process and provide flexibility. Further, owing to a large variety of existing registration algorithms, such an approach that is usable on any algorithm may be useful

    MulViMotion: shape-aware 3D myocardial motion tracking from multi-view cardiac MRI

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    Recovering the 3D motion of the heart from cine cardiac magnetic resonance (CMR) imaging enables the assessment of regional myocardial function and is important for understanding and analyzing cardiovascular disease. However, 3D cardiac motion estimation is challenging because the acquired cine CMR images are usually 2D slices which limit the accurate estimation of through-plane motion. To address this problem, we propose a novel multi-view motion estimation network (MulViMotion), which integrates 2D cine CMR images acquired in short-axis and long-axis planes to learn a consistent 3D motion field of the heart. In the proposed method, a hybrid 2D/3D network is built to generate dense 3D motion fields by learning fused representations from multi-view images. To ensure that the motion estimation is consistent in 3D, a shape regularization module is introduced during training, where shape information from multi-view images is exploited to provide weak supervision to 3D motion estimation. We extensively evaluate the proposed method on 2D cine CMR images from 580 subjects of the UK Biobank study for 3D motion tracking of the left ventricular myocardium. Experimental results show that the proposed method quantitatively and qualitatively outperforms competing methods

    Spatio-Temporal Tensor Decomposition of a Polyaffine Motion Model for a Better Analysis of Pathological Left Ventricular Dynamics

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    International audienceGiven that heart disease can cause abnormal motion dynamics over the cardiac cycle, which can then affect cardiac function, understanding and quantifying cardiac motion can provide insight for clinicians to aid in diagnosis, therapy planning, as well as to determine the prognosis for a given patient. The goal of this paper is to extract population-specific cardiac motion patterns from 3D displacements in order to firstly identify the mean motion behaviour in a population and secondly to describe pathology-specific motion patterns in terms of the spatial and temporal aspects of the motion. Since there are common motion patterns observed in patients suffering from the same condition, extracting these patterns can lead towards a better understanding of a disease. Quantifying cardiac motion at a population level is not a simple task since images can vary widely in terms of image quality, size, resolution and pose. To overcome this, we analyse the parameters obtained from a cardiac-specific Polyaffine motion tracking algorithm, which are aligned both spatially and temporally to a common reference space. Once all parameters are aligned, different subjects and different populations can be compared and analysed in the space of Polyaffine transformations by projecting the transformations to a reduced-order subspace in which dominant motion patterns in each population can be extracted and analysed. Using tensor decomposition allows the spatial and temporal aspects to be decoupled in order to study the different components individually. The proposed method was validated on healthy volunteers and Tetralogy of Fallot patients according to known spatial andtemporal behaviour for each population. A key advantage of the proposed method is the ability to regenerate motion sequences from the respective models, thus the models can be visualised in terms of the full motion, which allows for better understanding of the motion dynamics of different populations
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