463 research outputs found
Recommendations to improve imaging and analysis of brain lesion load and atrophy in longitudinal studies of multiple sclerosis
Focal lesions and brain atrophy are the most extensively studied aspects of multiple sclerosis (MS), but the image acquisition and analysis techniques used can be further improved, especially those for studying within-patient changes of lesion load and atrophy longitudinally. Improved accuracy and sensitivity will reduce the numbers of patients required to detect a given treatment effect in a trial, and ultimately, will allow reliable characterization of individual patients for personalized treatment. Based on open issues in the field of MS research, and the current state of the art in magnetic resonance image analysis methods for assessing brain lesion load and atrophy, this paper makes recommendations to improve these measures for longitudinal studies of MS. Briefly, they are (1) images should be acquired using 3D pulse sequences, with near-isotropic spatial resolution and multiple image contrasts to allow more comprehensive analyses of lesion load and atrophy, across timepoints. Image artifacts need special attention given their effects on image analysis results. (2) Automated image segmentation methods integrating the assessment of lesion load and atrophy are desirable. (3) A standard dataset with benchmark results should be set up to facilitate development, calibration, and objective evaluation of image analysis methods for MS
Quantitative Evaluation of Intensity Inhomogeneity Correction Methods for Structural MR Brain Images
Atlas-based automated positioning of outer volume suppression slices in short-TE 3D MR spectroscopic imaging of the human brain
Spatial suppression of peripheral lipid-containing regions in volumetric MR spectroscopic imaging (MRSI) of the human brain requires placing large numbers of outer volume suppression (OVS) slices, which is time consuming, prone to operator error and may introduce subject-dependent variability in volume coverage. We developed a novel, computationally efficient atlas-based approach for automated positioning of up to 16 OVS slices and the MRSI slab. Standardized positions in MNI atlas space were established offline using a recently developed iterative optimization procedure. During the scanning session, positions in subject space were computed using affine transformation of standardized positions in MNI space. This atlas-based approach was characterized offline using MPRAGE data collected in 11 subjects. The method was further validated in 14 subjects on a clinical 3T scanner using 3D short TE (15-20ms) Proton-Echo-Planar-Spectroscopic-Imaging (PEPSI) in upper cerebrum. Comparison of manual and automatic placement using 8 OVS slices demonstrated consistent MRSI volume selection and comparable spectral quality with similar degree of lipid suppression and number of usable voxels. Automated positioning of 16 OVS slices enabled larger volume coverage, while maintaining similar spectral quality and lipid suppression. Atlas-based automatic prescription of short TE MRSI is expected to be advantageous for longitudinal and cross sectional studiesThis work was supported in part by the
MIND Research Network (DOE Grant No. DE-FG02-99ER62764) and the University of
New Mexico School of Medicine Brain and Behavioral Illness Signature Program.Publicad
Quantitation in MRI : application to ageing and epilepsy
Multi-atlas propagation and label fusion techniques have recently been developed for segmenting
the human brain into multiple anatomical regions. In this thesis, I investigate
possible adaptations of these current state-of-the-art methods. The aim is to study ageing
on the one hand, and on the other hand temporal lobe epilepsy as an example for a
neurological disease.
Overall effects are a confounding factor in such anatomical analyses. Intracranial volume
(ICV) is often preferred to normalize for global effects as it allows to normalize for estimated
maximum brain size and is hence independent of global brain volume loss, as seen
in ageing and disease. I describe systematic differences in ICV measures obtained at 1.5T
versus 3T, and present an automated method of measuring intracranial volume, Reverse
MNI Brain Masking (RBM), based on tissue probability maps in MNI standard space. I
show that this is comparable to manual measurements and robust against field strength
differences.
Correct and robust segmentation of target brains which show gross abnormalities, such as
ventriculomegaly, is important for the study of ageing and disease. We achieved this with
incorporating tissue classification information into the image registration process. The
best results in elderly subjects, patients with TLE and healthy controls were achieved using
a new approach using multi-atlas propagation with enhanced registration (MAPER).
I then applied MAPER to the problem of automatically distinguishing patients with TLE
with (TLE-HA) and without (TLE-N) hippocampal atrophy on MRI from controls, and
determine the side of seizure onset. MAPER-derived structural volumes were used for
a classification step consisting of selecting a set of discriminatory structures and applying
support vector machine on the structural volumes as well as morphological similarity
information such as volume difference obtained with spectral analysis. Acccuracies were
91-100 %, indicating that the method might be clinically useful.
Finally, I used the methods developed in the previous chapters to investigate brain regional
volume changes across the human lifespan in over 500 healthy subjects between 20
to 90 years of age, using data from three different scanners (2x 1.5T, 1x 3T), using the IXI
database. We were able to confirm several known changes, indicating the veracity of the
method. In addition, we describe the first multi-region, whole-brain database of normal
ageing
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
An improved version of white matter method for correction of non-uniform intensity in MR images: application to the quantification of rates of brain atrophy in Alzheimer's disease and normal aging
A fully automated 3D version of the so-called white matter method for correcting intensity non-uniformity in MR T1-weighted neuro images is presented. The algorithm is an extension of the original work published previously. The major part of the extension was the development of a fully automated method for the generation of the reference points. In the design of this method, a number of measures were introduced to minimize the effects of possible inclusion of non-white matter voxels in the selection process. The correction process has been made iterative. PI drawback of this approach is an increased cost in computational time. The algorithm has been tested on T1-weighted MR images acquired from a longitudinal study involving elderly subjects and people with probable Alzheimer's disease. More quantitative measures were used for the evaluation of the algorithm's performance. Highly satisfactory correction results have been obtained for images with extensive intensity non-uniformity either present in raw data or added artificially. With intensity correction, improved accuracy in the measurement of the rate of brain atrophy in Alzheimer's patients as well as in elderly people due to normal aging has been achieved
Boosting multiple sclerosis lesion segmentation through attention mechanism
Magnetic resonance imaging is a fundamental tool to reach a diagnosis of
multiple sclerosis and monitoring its progression. Although several attempts
have been made to segment multiple sclerosis lesions using artificial
intelligence, fully automated analysis is not yet available. State-of-the-art
methods rely on slight variations in segmentation architectures (e.g. U-Net,
etc.). However, recent research has demonstrated how exploiting temporal-aware
features and attention mechanisms can provide a significant boost to
traditional architectures. This paper proposes a framework that exploits an
augmented U-Net architecture with a convolutional long short-term memory layer
and attention mechanism which is able to segment and quantify multiple
sclerosis lesions detected in magnetic resonance images. Quantitative and
qualitative evaluation on challenging examples demonstrated how the method
outperforms previous state-of-the-art approaches, reporting an overall Dice
score of 89% and also demonstrating robustness and generalization ability on
never seen new test samples of a new dedicated under construction dataset
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
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