9,631 research outputs found
Computerized Analysis of Magnetic Resonance Images to Study Cerebral Anatomy in Developing Neonates
The study of cerebral anatomy in developing neonates is of great importance for
the understanding of brain development during the early period of life. This
dissertation therefore focuses on three challenges in the modelling of cerebral
anatomy in neonates during brain development. The methods that have been
developed all use Magnetic Resonance Images (MRI) as source data.
To facilitate study of vascular development in the neonatal period, a set of image
analysis algorithms are developed to automatically extract and model cerebral
vessel trees. The whole process consists of cerebral vessel tracking from
automatically placed seed points, vessel tree generation, and vasculature
registration and matching. These algorithms have been tested on clinical Time-of-
Flight (TOF) MR angiographic datasets.
To facilitate study of the neonatal cortex a complete cerebral cortex segmentation
and reconstruction pipeline has been developed. Segmentation of the neonatal
cortex is not effectively done by existing algorithms designed for the adult brain
because the contrast between grey and white matter is reversed. This causes pixels
containing tissue mixtures to be incorrectly labelled by conventional methods. The
neonatal cortical segmentation method that has been developed is based on a novel
expectation-maximization (EM) method with explicit correction for mislabelled
partial volume voxels. Based on the resulting cortical segmentation, an implicit
surface evolution technique is adopted for the reconstruction of the cortex in
neonates. The performance of the method is investigated by performing a detailed
landmark study.
To facilitate study of cortical development, a cortical surface registration algorithm
for aligning the cortical surface is developed. The method first inflates extracted
cortical surfaces and then performs a non-rigid surface registration using free-form
deformations (FFDs) to remove residual alignment. Validation experiments using
data labelled by an expert observer demonstrate that the method can capture local
changes and follow the growth of specific sulcus
Groupwise Multimodal Image Registration using Joint Total Variation
In medical imaging it is common practice to acquire a wide range of
modalities (MRI, CT, PET, etc.), to highlight different structures or
pathologies. As patient movement between scans or scanning session is
unavoidable, registration is often an essential step before any subsequent
image analysis. In this paper, we introduce a cost function based on joint
total variation for such multimodal image registration. This cost function has
the advantage of enabling principled, groupwise alignment of multiple images,
whilst being insensitive to strong intensity non-uniformities. We evaluate our
algorithm on rigidly aligning both simulated and real 3D brain scans. This
validation shows robustness to strong intensity non-uniformities and low
registration errors for CT/PET to MRI alignment. Our implementation is publicly
available at https://github.com/brudfors/coregistration-njtv
Joint Total Variation ESTATICS for Robust Multi-Parameter Mapping
Quantitative magnetic resonance imaging (qMRI) derives tissue-specific
parameters -- such as the apparent transverse relaxation rate R2*, the
longitudinal relaxation rate R1 and the magnetisation transfer saturation --
that can be compared across sites and scanners and carry important information
about the underlying microstructure. The multi-parameter mapping (MPM) protocol
takes advantage of multi-echo acquisitions with variable flip angles to extract
these parameters in a clinically acceptable scan time. In this context,
ESTATICS performs a joint loglinear fit of multiple echo series to extract R2*
and multiple extrapolated intercepts, thereby improving robustness to motion
and decreasing the variance of the estimators. In this paper, we extend this
model in two ways: (1) by introducing a joint total variation (JTV) prior on
the intercepts and decay, and (2) by deriving a nonlinear maximum \emph{a
posteriori} estimate. We evaluated the proposed algorithm by predicting
left-out echoes in a rich single-subject dataset. In this validation, we
outperformed other state-of-the-art methods and additionally showed that the
proposed approach greatly reduces the variance of the estimated maps, without
introducing bias.Comment: 11 pages, 2 figures, 1 table, conference paper, accepted at MICCAI
202
Intensity Segmentation of the Human Brain with Tissue dependent Homogenization
High-precision segmentation of the human cerebral cortex based on T1-weighted MRI is still a challenging task. When opting to use an intensity based approach, careful data processing is mandatory to overcome inaccuracies. They are caused by noise, partial volume effects and systematic signal intensity variations imposed by limited homogeneity of the acquisition hardware. We propose an intensity segmentation which is free from any shape prior. It uses for the first time alternatively grey (GM) or white matter (WM) based homogenization. This new tissue dependency was introduced as the analysis of 60 high resolution MRI datasets revealed appreciable differences in the axial bias field corrections, depending if they are based on GM or WM. Homogenization starts with axial bias correction, a spatially irregular distortion correction follows and finally a noise reduction is applied. The construction of the axial bias correction is based on partitions of a depth histogram. The irregular bias is modelled by Moody Darken radial basis functions. Noise is eliminated by nonlinear edge preserving and homogenizing filters. A critical point is the estimation of the training set for the irregular bias correction in the GM approach. Because of intensity edges between CSF (cerebro spinal fluid surrounding the brain and within the ventricles), GM and WM this estimate shows an acceptable stability. By this supervised approach a high flexibility and precision for the segmentation of normal and pathologic brains is gained. The precision of this approach is shown using the Montreal brain phantom. Real data applications exemplify the advantage of the GM based approach, compared to the usual WM homogenization, allowing improved cortex segmentation
Segmentation of brain MRI during early childhood
The objective of this thesis is the development of automatic methods to measure the changes in
volume and growth of brain structures in prematurely born infants. Automatic tools for accurate
tissue quantification from magnetic resonance images can provide means for understanding
how the neurodevelopmental effects of the premature birth, such as cognitive, neurological or
behavioural impairment, are related to underlying changes in brain anatomy. Understanding
these changes forms a basis for development of suitable treatments to improve the outcomes of
premature birth.
In this thesis we focus on the segmentation of brain structures from magnetic resonance images
during early childhood. Most of the current brain segmentation techniques have been focused
on the segmentation of adult or neonatal brains. As a result of rapid development, the brain
anatomy during early childhood differs from anatomy of both adult and neonatal brains and
therefore requires adaptations of available techniques to produce good results.
To address the issue of anatomical differences of the brain during early childhood compared
to other age-groups, population-specific deformable and probabilistic atlases are introduced. A
method for generation of population-specific prior information in form of a probabilistic atlas
is proposed and used to enhance existing segmentation algorithms.
The evaluation of registration-based and intensity-based approaches shows the techniques to
be complementary in the quality of automatic segmentation in different parts of the brain. We
propose a novel robust segmentation method combining the advantages of both approaches. The
method is based on multiple label propagation using B-spline non-rigid registration followed by
EM segmentation.
Intensity inhomogeneity is a shading artefact resulting from the acquisition process, which
significantly affects modern high resolution MR data acquired at higher magnetic field strengths.
A novel template based method focused on correcting the intensity inhomogeneity in data
acquired at higher magnetic field strengths is therefore proposed.
The proposed segmentation method combined with proposed intensity inhomogeneity correction
method offers a robust tool for quantification of volumes and growth of brain structures during
early childhood. The tool have been applied to 67 T1-weigted images of subject at one and two years of age
Keypoint Transfer for Fast Whole-Body Segmentation
We introduce an approach for image segmentation based on sparse
correspondences between keypoints in testing and training images. Keypoints
represent automatically identified distinctive image locations, where each
keypoint correspondence suggests a transformation between images. We use these
correspondences to transfer label maps of entire organs from the training
images to the test image. The keypoint transfer algorithm includes three steps:
(i) keypoint matching, (ii) voting-based keypoint labeling, and (iii)
keypoint-based probabilistic transfer of organ segmentations. We report
segmentation results for abdominal organs in whole-body CT and MRI, as well as
in contrast-enhanced CT and MRI. Our method offers a speed-up of about three
orders of magnitude in comparison to common multi-atlas segmentation, while
achieving an accuracy that compares favorably. Moreover, keypoint transfer does
not require the registration to an atlas or a training phase. Finally, the
method allows for the segmentation of scans with highly variable field-of-view.Comment: Accepted for publication at IEEE Transactions on Medical Imagin
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