746 research outputs found

    Diffusion kurtosis imaging based on adaptive spherical integral

    Get PDF
    Diffusion kurtosis imaging (DKI) is a recent approach in medical engineering that has potential value for both neurological diseases and basic neuroscience research. In this letter, we develop a robust method based on adaptive spherical integral that can compute kurtosis based quantities more precisely and efficiently. Our method integrates spherical trigonometry with a recursive computational scheme to make numerical estimations in kurtosis imaging convergent. Our algorithm improves the efficiency of computing integral invariants based on reconstructed diffusion kurtosis tensors and makes DKI better prepared for further clinical applications. © 2011 IEEE.link_to_subscribed_fulltex

    Rotationally-invariant mapping of scalar and orientational metrics of neuronal microstructure with diffusion MRI

    Full text link
    We develop a general analytical and numerical framework for estimating intra- and extra-neurite water fractions and diffusion coefficients, as well as neurite orientational dispersion, in each imaging voxel. By employing a set of rotational invariants and their expansion in the powers of diffusion weighting, we analytically uncover the nontrivial topology of the parameter estimation landscape, showing that multiple branches of parameters describe the measurement almost equally well, with only one of them corresponding to the biophysical reality. A comprehensive acquisition shows that the branch choice varies across the brain. Our framework reveals hidden degeneracies in MRI parameter estimation for neuronal tissue, provides microstructural and orientational maps in the whole brain without constraints or priors, and connects modern biophysical modeling with clinical MRI.Comment: 25 pages, 12 figures, elsarticle two-colum

    Efficient estimation of propagator anisotropy and non‐Gaussianity in multishell diffusion MRI with micro‐structure adaptive convolution kernels and dual Fourier integral transforms

    Get PDF
    Producción CientíficaPurpose:We seek to reformulate the so-called Propagator Anisotropy (PA) andNon-Gaussianity (NG), originally conceived for the Mean Apparent Propagatordiffusion MRI (MAP-MRI), to the Micro-Structure adaptive convolution ker-nels and dual Fourier Integral Transforms (MiSFIT). These measures describerelevant normalized features of the Ensemble Average Propagator (EAP).Theory and Methods:First, the indices, which are defined as the EAP’sdissimilarity from an isotropic (PA) or a Gaussian (NG) one, are analyticallyreformulated within the MiSFIT framework. Then a comparison between theresulting maps is drawn by means of a visual analysis, a quantitative assess-ment via numerical simulations, a test-retest study across the MICRA dataset (6subjects scanned five times) and, finally, a computational time evaluation.Results:Findings illustrate the visual similarity between the indices computedwith either technique. Evaluation against synthetic ground truth data, however,demonstrates MiSFIT’s improved accuracy. In addition, the test–retest studyreveals MiSFIT’s higher degree of reliability in most of white matter regions.Finally, the computational time evaluation shows MiSFIT’s time reduction upto two orders of magnitude.Conclusions:Despite being a direct development on the MAP-MRI represen-tation, the PA and the NG can be reliably and efficiently computed withinMiSFIT’s framework. This, together with the previous findings in the originalMiSFIT’s article, could mean the difference that definitely qualifies diffusionMRI to be incorporated into regular clinical settings.Ministerio de Educación, Junta de Castilla y León y Fondo Social Europeo, (Grant/Award Number: OrdenEDU/1100/2017 12/12)Ministerio de Ciencia e Innovación, Grant/AwardNumbers: (RTI2018-094569-B-I00),(PID2021-124407NB-I00)Ministry of Science and Higher Education of Poland,(Grant/Award Number:692/STYP/13/2018)Narodowa Agencja Wymiany Akademickiej, (Grant/AwardNumber: PPN/BEK/2019/1/00421

    Model-based analysis of multishell diffusion MR data for tractography: how to get over fitting problems

    Get PDF
    In this article, we highlight an issue that arises when using multiple b‐values in a model‐based analysis of diffusion MR data for tractography. The non‐monoexponential decay, commonly observed in experimental data, is shown to induce overfitting in the distribution of fiber orientations when not considered in the model. Extra fiber orientations perpendicular to the main orientation arise to compensate for the slower apparent signal decay at higher b‐values. We propose a simple extension to the ball and stick model based on a continuous gamma distribution of diffusivities, which significantly improves the fitting and reduces the overfitting. Using in vivo experimental data, we show that this model outperforms a simpler, noise floor model, especially at the interfaces between brain tissues, suggesting that partial volume effects are a major cause of the observed non‐monoexponential decay. This model may be helpful for future data acquisition strategies that may attempt to combine multiple shells to improve estimates of fiber orientations in white matter and near the cortex

    Numerical simulation of diffusion MRI signals using an adaptive time-stepping method

    Get PDF
    International audienceThe effect on the MRI signal of water diffusion in biological tissues in the presence of applied magnetic field gradient pulses can be modelled by a multiple compartment Bloch-Torrey partial differential equation. We present a method for the numerical solution of this equation by coupling a standard Cartesian spatial discretization with an adaptive time discretization. The time discretization is done using the explicit Runge-Kutta-Chebyshev method, which is more efficient than the forward Euler time discretization for diffusive-type problems. We use this approach to simulate the diffusion MRI signal from the extra-cylindrical compartment in a tissue model of the brain gray matter consisting of cylindrical and spherical cells and illustrate the effect of cell membrane permeability

    Development of Advanced, Clinically Feasible Neuroimaging Methodology with Diffusional Kurtosis Imaging

    Get PDF
    Diffusion MRI (dMRI) is a powerful, non-invasive tool for probing the structural organization of the human brain. Quantitative dMRI analyses provide unique capabilities for the characterization of tissue microstructure as well as imaging contrast that is not available to other modalities. White matter tractography relies on dMRI and is currently the only non-invasive technique for mapping structural connections in the human brain. In this chapter, we will describe diffusional kurtosis imaging, an effective and versatile dMRI technique, and discuss a clinical problem in temporal lobe epilepsy (TLE) which is insurmountable with current diagnostic approaches. Subsequent chapters will further develop the capabilities of DKI and demonstrate how it may be particularly well suited to overcome current barriers to care in the clinical management of TLE

    Adaptive smoothing of multi-shell diffusion-weighted magnetic resonance data by msPOAS

    Get PDF
    In this article we present a noise reduction method (msPOAS) for multi-shell diffusion-weighted magnetic resonance data. To our knowledge, this is the first smoothing method which allows simultaneous smoothing of all q-shells. It is applied directly to the diffusion weighted data and consequently allows subsequent analysis by any model. Due to its adaptivity, the procedure avoids blurring of the inherent structures and preserves discontinuities. MsPOAS extends the recently developed position-orientation adaptive smoothing (POAS) procedure to multi-shell experiments. At the same time it considerably simplifies and accelerates the calculations. The behavior of the algorithm msPOAS is evaluated on diffusion-weighted data measured on a single shell and on multiple shells

    Diffusional Kurtosis Imaging in the Diffusion Imaging in Python Project.

    Get PDF
    Diffusion-weighted magnetic resonance imaging (dMRI) measurements and models provide information about brain connectivity and are sensitive to the physical properties of tissue microstructure. Diffusional Kurtosis Imaging (DKI) quantifies the degree of non-Gaussian diffusion in biological tissue from dMRI. These estimates are of interest because they were shown to be more sensitive to microstructural alterations in health and diseases than measures based on the total anisotropy of diffusion which are highly confounded by tissue dispersion and fiber crossings. In this work, we implemented DKI in the Diffusion in Python (DIPY) project-a large collaborative open-source project which aims to provide well-tested, well-documented and comprehensive implementation of different dMRI techniques. We demonstrate the functionality of our methods in numerical simulations with known ground truth parameters and in openly available datasets. A particular strength of our DKI implementations is that it pursues several extensions of the model that connect it explicitly with microstructural models and the reconstruction of 3D white matter fiber bundles (tractography). For instance, our implementations include DKI-based microstructural models that allow the estimation of biophysical parameters, such as axonal water fraction. Moreover, we illustrate how DKI provides more general characterization of non-Gaussian diffusion compatible with complex white matter fiber architectures and gray matter, and we include a novel mean kurtosis index that is invariant to the confounding effects due to tissue dispersion. In summary, DKI in DIPY provides a well-tested, well-documented and comprehensive reference implementation for DKI. It provides a platform for wider use of DKI in research on brain disorders and in cognitive neuroscience

    Higher-Order Tensors and Differential Topology in Diffusion MRI Modeling and Visualization

    Get PDF
    Diffusion Weighted Magnetic Resonance Imaging (DW-MRI) is a noninvasive method for creating three-dimensional scans of the human brain. It originated mostly in the 1970s and started its use in clinical applications in the 1980s. Due to its low risk and relatively high image quality it proved to be an indispensable tool for studying medical conditions as well as for general scientific research. For example, it allows to map fiber bundles, the major neuronal pathways through the brain. But all evaluation of scanned data depends on mathematical signal models that describe the raw signal output and map it to biologically more meaningful values. And here we find the most potential for improvement. In this thesis we first present a new multi-tensor kurtosis signal model for DW-MRI. That means it can detect multiple overlapping fiber bundles and map them to a set of tensors. Compared to other already widely used multi-tensor models, we also add higher order kurtosis terms to each fiber. This gives a more detailed quantification of fibers. These additional values can also be estimated by the Diffusion Kurtosis Imaging (DKI) method, but we show that these values are drastically affected by fiber crossings in DKI, whereas our model handles them as intrinsic properties of fiber bundles. This reduces the effects of fiber crossings and allows a more direct examination of fibers. Next, we take a closer look at spherical deconvolution. It can be seen as a generalization of multi-fiber signal models to a continuous distribution of fiber directions. To this approach we introduce a novel mathematical constraint. We show, that state-of-the-art methods for estimating the fiber distribution become more robust and gain accuracy when enforcing our constraint. Additionally, in the context of our own deconvolution scheme, it is algebraically equivalent to enforcing that the signal can be decomposed into fibers. This means, tractography and other methods that depend on identifying a discrete set of fiber directions greatly benefit from our constraint. Our third major contribution to DW-MRI deals with macroscopic structures of fiber bundle geometry. In recent years the question emerged, whether or not, crossing bundles form two-dimensional surfaces inside the brain. Although not completely obvious, there is a mathematical obstacle coming from differential topology, that prevents general tangential planes spanned by fiber directions at each point to be connected into consistent surfaces. Research into how well this constraint is fulfilled in our brain is hindered by the high precision and complexity needed by previous evaluation methods. This is why we present a drastically simpler method that negates the need for precisely finding fiber directions and instead only depends on the simple diffusion tensor method (DTI). We then use our new method to explore and improve streamsurface visualization.<br /

    Adaptive smoothing of multi-shell diffusion-weighted magnetic resonance data by msPOAS

    Get PDF
    In this article we present a noise reduction method (msPOAS) for multi-shell diffusion-weighted magnetic resonance data. To our knowledge, this is the first smoothing method which allows simultaneous smoothing of all q-shells. It is applied directly to the diffusion weighted data and consequently allows subsequent analysis by any model. Due to its adaptivity, the procedure avoids blurring of the inherent structures and preserves discontinuities. MsPOAS extends the recently developed position-orientation adaptive smoothing (POAS) procedure to multi-shell experiments. At the same time it considerably simplifies and accelerates the calculations. The behavior of the algorithm msPOAS is evaluated on diffusion-weighted data measured on a single shell and on multiple shells
    corecore