534 research outputs found
Characterising population variability in brain structure through models of whole-brain structural connectivity
Models of whole-brain connectivity are valuable for understanding neurological function. This thesis
seeks to develop an optimal framework for extracting models of whole-brain connectivity from clinically
acquired diffusion data. We propose new approaches for studying these models. The aim is to
develop techniques which can take models of brain connectivity and use them to identify biomarkers
or phenotypes of disease.
The models of connectivity are extracted using a standard probabilistic tractography algorithm, modified
to assess the structural integrity of tracts, through estimates of white matter anisotropy. Connections
are traced between 77 regions of interest, automatically extracted by label propagation from
multiple brain atlases followed by classifier fusion. The estimates of tissue integrity for each tract
are input as indices in 77x77 ”connectivity” matrices, extracted for large populations of clinical data.
These are compared in subsequent studies.
To date, most whole-brain connectivity studies have characterised population differences using graph
theory techniques. However these can be limited in their ability to pinpoint the locations of differences
in the underlying neural anatomy. Therefore, this thesis proposes new techniques. These include
a spectral clustering approach for comparing population differences in the clustering properties of
weighted brain networks. In addition, machine learning approaches are suggested for the first time.
These are particularly advantageous as they allow classification of subjects and extraction of features
which best represent the differences between groups.
One limitation of the proposed approach is that errors propagate from segmentation and registration
steps prior to tractography. This can cumulate in the assignment of false positive connections, where
the contribution of these factors may vary across populations, causing the appearance of population
differences where there are none. The final contribution of this thesis is therefore to develop a common
co-ordinate space approach. This combines probabilistic models of voxel-wise diffusion for each subject
into a single probabilistic model of diffusion for the population. This allows tractography to be
performed only once, ensuring that there is one model of connectivity. Cross-subject differences can
then be identified by mapping individual subjects’ anisotropy data to this model. The approach is
used to compare populations separated by age and gender
Estimation of Fiber Orientations Using Neighborhood Information
Data from diffusion magnetic resonance imaging (dMRI) can be used to
reconstruct fiber tracts, for example, in muscle and white matter. Estimation
of fiber orientations (FOs) is a crucial step in the reconstruction process and
these estimates can be corrupted by noise. In this paper, a new method called
Fiber Orientation Reconstruction using Neighborhood Information (FORNI) is
described and shown to reduce the effects of noise and improve FO estimation
performance by incorporating spatial consistency. FORNI uses a fixed tensor
basis to model the diffusion weighted signals, which has the advantage of
providing an explicit relationship between the basis vectors and the FOs. FO
spatial coherence is encouraged using weighted l1-norm regularization terms,
which contain the interaction of directional information between neighbor
voxels. Data fidelity is encouraged using a squared error between the observed
and reconstructed diffusion weighted signals. After appropriate weighting of
these competing objectives, the resulting objective function is minimized using
a block coordinate descent algorithm, and a straightforward parallelization
strategy is used to speed up processing. Experiments were performed on a
digital crossing phantom, ex vivo tongue dMRI data, and in vivo brain dMRI data
for both qualitative and quantitative evaluation. The results demonstrate that
FORNI improves the quality of FO estimation over other state of the art
algorithms.Comment: Journal paper accepted in Medical Image Analysis. 35 pages and 16
figure
Improving Fiber Alignment in HARDI by Combining Contextual PDE Flow with Constrained Spherical Deconvolution
We propose two strategies to improve the quality of tractography results
computed from diffusion weighted magnetic resonance imaging (DW-MRI) data. Both
methods are based on the same PDE framework, defined in the coupled space of
positions and orientations, associated with a stochastic process describing the
enhancement of elongated structures while preserving crossing structures. In
the first method we use the enhancement PDE for contextual regularization of a
fiber orientation distribution (FOD) that is obtained on individual voxels from
high angular resolution diffusion imaging (HARDI) data via constrained
spherical deconvolution (CSD). Thereby we improve the FOD as input for
subsequent tractography. Secondly, we introduce the fiber to bundle coherence
(FBC), a measure for quantification of fiber alignment. The FBC is computed
from a tractography result using the same PDE framework and provides a
criterion for removing the spurious fibers. We validate the proposed
combination of CSD and enhancement on phantom data and on human data, acquired
with different scanning protocols. On the phantom data we find that PDE
enhancements improve both local metrics and global metrics of tractography
results, compared to CSD without enhancements. On the human data we show that
the enhancements allow for a better reconstruction of crossing fiber bundles
and they reduce the variability of the tractography output with respect to the
acquisition parameters. Finally, we show that both the enhancement of the FODs
and the use of the FBC measure on the tractography improve the stability with
respect to different stochastic realizations of probabilistic tractography.
This is shown in a clinical application: the reconstruction of the optic
radiation for epilepsy surgery planning
Measuring macroscopic brain connections in vivo
Decades of detailed anatomical tracer studies in non-human animals point to a rich and complex organization of long-range white matter connections in the brain. State-of-the art in vivo imaging techniques are striving to achieve a similar level of detail in humans, but multiple technical factors can limit their sensitivity and fidelity. In this review, we mostly focus on magnetic resonance imaging of the brain. We highlight some of the key challenges in analyzing and interpreting in vivo connectomics data, particularly in relation to what is known from classical neuroanatomy in laboratory animals. We further illustrate that, despite the challenges, in vivo imaging methods can be very powerful and provide information on connections that is not available by any other means
Adaptive microstructure-informed tractography for accurate brain connectivity analyses
Human brain has been subject of deep interest for centuries, given it's central role in controlling and directing the actions and functions of the body as response to external stimuli. The neural tissue is primarily constituted of neurons and, together with dendrites and the nerve synapses, constitute the gray matter (GM) which plays a major role in cognitive functions. The information processed in the GM travel from one region to the other of the brain along nerve cell projections, called axons. All together they constitute the white matter (WM) whose wiring organization still remains challenging to uncover. The relationship between structure organization of the brain and function has been deeply investigated on humans and animals based on the assumption that the anatomic architecture determine the network dynamics. In response to that, many different imaging techniques raised, among which diffusion-weighted magnetic resonance imaging (DW-MRI) has triggered tremendous hopes and expectations. Diffusion-weighted imaging measures both restricted and unrestricted diffusion, i.e. the degree of movement freedom of the water molecules, allowing to map the tissue fiber architecture in vivo and non-invasively. Based on DW-MRI data, tractography is able to exploit information of the local fiber orientation to recover global fiber pathways, called streamlines, that represent groups of axons. This, in turn, allows to infer the WM structural connectivity, becoming widely used in many different clinical applications as for diagnoses, virtual dissections and surgical planning. However, despite this unique and compelling ability, data acquisition still suffers from technical limitations and recent studies have highlighted the poor anatomical accuracy of the reconstructions obtained with this technique and challenged its effectiveness for studying brain connectivity. The focus of this Ph.D. project is to specifically address these limitations and to improve the anatomical accuracy of the structural connectivity estimates. To this aim, we developed a global optimization algorithm that exploits micro and macro-structure information, introducing an iterative procedure that uses the underlying tissue properties to drive the reconstruction using a semi-global approach. Then, we investigated the possibility to dynamically adapt the position of a set of candidate streamlines while embedding the anatomical prior of trajectories smoothness and adapting the configuration based on the observed data. Finally, we introduced the concept of bundle-o-graphy by implementing a method to model groups of streamlines based on the concept that axons are organized into fascicles, adapting their shape and extent based on the underlying microstructure
Computing and visualising intra-voxel orientation-specific relaxation-diffusion features in the human brain
Diffusion MRI techniques are used widely to study the characteristics of the human brain connectome in vivo. However, to resolve and characterise white matter (WM) fibres in heterogeneous MRI voxels remains a challenging problem typically approached with signal models that rely on prior information and constraints. We have recently introduced a 5D relaxation–diffusion correlation framework wherein multidimensional diffusion encoding strategies are used to acquire data at multiple echo‐times to increase the amount of information encoded into the signal and ease the constraints needed for signal inversion. Nonparametric Monte Carlo inversion of the resulting datasets yields 5D relaxation–diffusion distributions where contributions from different sub‐voxel tissue environments are separated with minimal assumptions on their microscopic properties. Here, we build on the 5D correlation approach to derive fibre‐specific metrics that can be mapped throughout the imaged brain volume. Distribution components ascribed to fibrous tissues are resolved, and subsequently mapped to a dense mesh of overlapping orientation bins to define a smooth orientation distribution function (ODF). Moreover, relaxation and diffusion measures are correlated to each independent ODF coordinate, thereby allowing the estimation of orientation‐specific relaxation rates and diffusivities. The proposed method is tested on a healthy volunteer, where the estimated ODFs were observed to capture major WM tracts, resolve fibre crossings, and, more importantly, inform on the relaxation and diffusion features along with distinct fibre bundles. If combined with fibre‐tracking algorithms, the methodology presented in this work has potential for increasing the depth of characterisation of microstructural properties along individual WM pathways
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