Biomedical subjects

Julia A Schnabel

Publications and source records attributed to Julia A Schnabel.

7 recordsLinked to original sources

PubMed2006

Phenomenological model of diffuse global and regional atrophy using finite-element methods.

The main goal of this work is the generation of ground-truth data for the validation of atrophy measurement techniques, commonly used in the study of neurodegenerative diseases such as dementia. Several techniques have been used to measure atrophy in cross-sectional and longitudinal studies, but it is extremely difficult to compare their performance since they have been applied to different patient populations. Furthermore, assessment of performance based on phantom measurements or simple scaled images overestimates these techniques' ability to capture the complexity of neurodegeneration of the human brain. We propose a method for atrophy simulation in structural magnetic resonance (MR) images based on finite-element methods. The method produces cohorts of brain images with known change that is physically and clinically plausible, providing data for objective evaluation of atrophy measurement techniques. Atrophy is simulated in different tissue compartments or in different neuroanatomical structures with a phenomenological model. This model of diffuse global and regional atrophy is based on volumetric measurements such as the brain or the hippocampus, from patients with known disease and guided by clinical knowledge of the relative pathological involvement of regions and tissues. The consequent biomechanical readjustment of structures is modelled using conventional physics-based techniques based on biomechanical tissue properties and simulating plausible tissue deformations with finite-element methods. A thermoelastic model of tissue deformation is employed, controlling the rate of progression of atrophy by means of a set of thermal coefficients, each one corresponding to a different type of tissue. Tissue characterization is performed by means of the meshing of a labelled brain atlas, creating a reference volumetric mesh that will be introduced to a finite-element solver to create the simulated deformations. Preliminary work on the simulation of acquisition artefacts is also presented. Cross-sectional and longitudinal sets of simulated data are shown and a visual classification protocol has been used by experts to rate real and simulated scans according to their degree of atrophy. Results confirm the potential of the proposed methodology.

Alzheimer Disease↗

PubMed2006

Factors influencing the accuracy of biomechanical breast models.

Recently it has been suggested that finite element methods could be used to predict breast deformations in a number of applications, including comparison of multimodality images, validation of image registration and image guided interventions. Unfortunately knowledge of the mechanical properties of breast tissues is limited. This study evaluated the accuracy with which biomechanical breast models based on finite element methods can predict the displacements of tissue within the breast in the practical clinical situation where the boundaries of the organ might be known reasonably accurately but there is some uncertainty on the mechanical properties of the tissue. For two datasets, we investigate the influence of tissue elasticity values, Poisson's ratios, boundary conditions, finite element solvers and mesh resolutions. Magnetic resonance images were acquired before and after compressing each volunteer's breast by about 20%. Surface displacement boundary conditions were derived from a three-dimensional nonrigid image registration. Six linear and three nonlinear elastic material models with and without skin were tested. These were compared to hyperelastic models. The accuracy of the models was evaluated by assessing the ability of the model to predict the location of 12 corresponding anatomical landmarks. The accuracy was most sensitive to the Poisson's ratio and the boundary condition. Best results were achieved for accurate boundary conditions, appropriate Poisson's ratios and models where fibroglandular tissue was at most four times stiffer than fatty tissue. These configurations reduced the mean (maximum) distance of the landmarks from 6.6 mm (12.4 mm) to 2.1 mm (3.4 mm) averaged over all experiments.

Algorithms↗

PubMed2003

Myocardial delineation via registration in a polar coordinate system.

RATIONALE AND OBJECTIVES: Cardiovascular disease is the number one cause of premature death in the western world. Analysis of cardiac function provides clinically useful diagnostic and prognostic information; however, manual analysis of function via delineation is prohibitively time consuming. This article describes a technique for analysis of dynamic magnetic resonance images of the left ventricle using a non-rigid registration algorithm. A manually delineated contour of a single phase was propagated through the dynamic sequence. MATERIALS AND METHODS: Short-axis cine magnetic resonance images were resampled into polar coordinates before all the time frames were aligned using a non-rigid registration algorithm. The technique was tested on 10 patient data sets, a total of 1,052 images were analyzed. RESULTS: Results of this approach were investigated and compared with manual delineation at all phases in the cardiac cycle, and with registration performed in a Cartesian coordinate system. The results correlated very well with manually delineated contours. CONCLUSION: A novel approach to the registration and subsequent delineation of cardiac magnetic resonance images has been introduced. For the endocardium, the polar resampling technique correlated well with manual delineation, and better than for images registered without radial resampling in a Cartesian coordinate system. For the epicardium, the difference was not as apparent with both techniques correlating well.

Algorithms↗

PubMed2003

Validation of nonrigid image registration using finite-element methods: application to breast MR images.

This paper presents a novel method for validation of nonrigid medical image registration. This method is based on the simulation of physically plausible, biomechanical tissue deformations using finite-element methods. Applying a range of displacements to finite-element models of different patient anatomies generates model solutions which simulate gold standard deformations. From these solutions, deformed images are generated with a range of deformations typical of those likely to occur in vivo. The registration accuracy with respect to the finite-element simulations is quantified by co-registering the deformed images with the original images and comparing the recovered voxel displacements with the biomechanically simulated ones. The functionality of the validation method is demonstrated for a previously described nonrigid image registration technique based on free-form deformations using B-splines and normalized mutual information as a voxel similarity measure, with an application to contrast-enhanced magnetic resonance mammography image pairs. The exemplar nonrigid registration technique is shown to be of subvoxel accuracy on average for this particular application. The validation method presented here is an important step toward more generic simulations of biomechanically plausible tissue deformations and quantification of tissue motion recovery using nonrigid image registration. It will provide a basis for improving and comparing different nonrigid registration techniques for a diversity of medical applications, such as intrasubject tissue deformation or motion correction in the brain, liver or heart.

Artifacts↗

PubMed2003

Automatic construction of 3-D statistical deformation models of the brain using nonrigid registration.

In this paper, we show how the concept of statistical deformation models (SDMs) can be used for the construction of average models of the anatomy and their variability. SDMs are built by performing a statistical analysis of the deformations required to map anatomical features in one subject into the corresponding features in another subject. The concept of SDMs is similar to statistical shape models (SSMs) which capture statistical information about shapes across a population, but offers several advantages over SSMs. First, SDMs can be constructed directly from images such as three-dimensional (3-D) magnetic resonance (MR) or computer tomography volumes without the need for segmentation which is usually a prerequisite for the construction of SSMs. Instead, a nonrigid registration algorithm based on free-form deformations and normalized mutual information is used to compute the deformations required to establish dense correspondences between the reference subject and the subjects in the population class under investigation. Second, SDMs allow the construction of an atlas of the average anatomy as well as its variability across a population of subjects. Finally, SDMs take the 3-D nature of the underlying anatomy into account by analysing dense 3-D deformation fields rather than only information about the surface shape of anatomical structures. We show results for the construction of anatomical models of the brain from the MR images of 25 different subjects. The correspondences obtained by the nonrigid registration are evaluated using anatomical landmark locations and show an average error of 1.40 mm at these anatomical landmark positions. We also demonstrate that SDMs can be constructed so as to minimize the bias toward the chosen reference subject.

Algorithms↗

PubMed2002

Automatic construction of multiple-object three-dimensional statistical shape models: application to cardiac modeling.

A novel method is introduced for the generation of landmarks for three-dimensional (3-D) shapes and the construction of the corresponding 3-D statistical shape models. Automatic landmarking of a set of manual segmentations from a class of shapes is achieved by 1) construction of an atlas of the class, 2) automatic extraction of the landmarks from the atlas, and 3) subsequent propagation of these landmarks to each example shape via a volumetric nonrigid registration technique using multiresolution B-spline deformations. This approach presents some advantages over previously published methods: it can treat multiple-part structures and requires less restrictive assumptions on the structure's topology. In this paper, we address the problem of building a 3-D statistical shape model of the left and right ventricle of the heart from 3-D magnetic resonance images. The average accuracy in landmark propagation is shown to be below 2.2 mm. This application demonstrates the robustness and accuracy of the method in the presence of large shape variability and multiple objects.

Algorithms↗

PubMed2002

Quantification of small cerebral ventricular volume changes in treated growth hormone patients using nonrigid registration.

Nonrigid registration can automatically quantify small changes in volume of anatomical structures over time by means of segmentation propagation. Here, we use a nonrigid registration algorithm based on optimising normalized mutual information to quantify small changes in brain ventricle volume in magnetic resonance (MR) images of a group of five patients treated with growth hormone replacement therapy and a control group of six volunteers. The lateral ventricles are segmented from each subject image by registering with the brainweb image which has this structure delineated. The mean (standard deviation) volume change measurements are 1.09 (0.73) cm3 for the patient group and 0.08 (0.62) cm3 for the volunteer group; this difference is statistically significant at the 1% level. We validate our volume measurements by determining the precision from three consecutive scans of five volunteers and also comparing the measurements to previously published volume change estimates obtained by visual inspection of difference images. Results demonstrate a precision of sigma < or = 0.52 cm3 (n = 5) and a rank correlation coefficient with assessed difference images of p = 0.7 (n = 11). To determine the level of shape correspondence we manually segmented subject's ventricles and compared them to the propagations using a voxel overlap similarity index, this gave a mean similarity index of 0.81 (n = 7).

Algorithms↗