Detection of developmental deficits in epileptic children using multimodal tensor decomposition techniques
Item Status
Restricted Access
Embargo End Date
2025-01-22
Date
Authors
Dron, Noramon
Abstract
Early childhood epilepsy can affect the child’s development and lead to developmental deficits.
Early detection and intervention are key to enabling the child to develop normally. Resting
state electroencephalogram (EEG) and Magnetic resonance imaging (MRI) are the main tools
clinicians use to diagnose children with epilepsy. This motivates us to take advantage of
these available data and jointly analyse them to explore the features related to developmental
deficits and predict the developmental scores of newly-onset patients. In particular, our work
considers EEG information, sMRI volumetric data, and psychometric evaluation scores. We
use matrix-tensor decompositions to analyse the shared features between each modality all
at once. This allows us to investigate the occurrence of shared profiles in EEG and sMRI
related to developmental impairment. Hence, this thesis develops data fusion methods based
on well-established tensor decomposition methods (canonical polyadic decomposition, CPD;
block term decomposition, BTD; and Tucker decomposition, TD). The methods are validated
in a publicly available dataset with healthy children (Child Mind Institute: CMI) and, more
importantly, in a local dataset of preschool children with epilepsy (NEUROPROFILE: Neu).
First, the thesis focuses on a CPD data fusion model, which decomposes the multi-way data
into a sum of rank-one factor matrices with the subject factor shared across three modalities.
The model is optimised via grid search. The CPD model reveals distinct features associated
with developmental deficits that agree with prior clinical knowledge. Then, we expand the
model through direct projection to predict the developmental scores from EEG and sMRI
data. A support vector machine (SVM) is used as a benchmark to compare the predicted score
performance. The result reveals CPD model is better at estimating the developmental scores
than the SVM. The CPD shows the feasibility of score prediction but still lacks the ability to
correctly identify the deficits, which highlights the need for a more flexible data fusion model.
Next, the thesis adopts block term decomposition (BTD) to bring in additional flexibility in the
modelling of the EEG tensor data. In BTD (Lᵣ,Lᵣ, 1), one mode of interest is fixed to rank
one while the others vary together to rank L. Subjects with missing scores and more sMRI
regions and sub-scores are included in this analysis. Bayesian optimisation is applied to reduce
the hyperparameter optimisation time. The results show that BTD (Lᵣ,Lᵣ, 1) can extract
additional features related to the deficits that the CPD model does not pick up. Then, we built
a model to predict the developmental scores. Overall, the prediction from BTD is generally
better than the CPD. However, the result shows both models may not be fully compatible with
EEG tensors and suggests the need for a better-fit model.
Therefore, we adopt TD as a flexible model for the EEG data. TD can decompose tensors into
factor matrices with different ranks interacting through a core tensor. However, TD without
constraints is not unique. Thus, we promote the sparseness in the TD core tensor in our
joint decomposition. In addition, we use structural connectivity information in the form of
diffusion tensor imaging (DTI) as a graph regularisation to the data fusion model to promote
interpretability. The effects of each constraint are investigated, and the most stable result is
extended to predict the scores. Since not all the patients have DTI data, the score prediction is
executed for both patients with and without DTI. Implementing the DTI graph regularisation
is found to result in predicted scores in a more plausible range. The sparse core TD with graph
regularisation performs best with the Neu dataset. However, some deficit patients are estimated
to score within the normal range, which does not fulfil the aim of identifying deficits accurately.
In addition, and given that the BTD (Lᵣ,Lᵣ, 1) tensor decomposition is closely related to
CPD, we investigate and expand the existing principle of CPD core consistency diagnosis
(CORCONDIA) to BTD (Lᵣ,Lᵣ, 1). BTDCORCONDIA is built to assist in determining
the number of components and the data compatibility to the model. The model is tested
with simulated and real EEG tensor data. We show that data generated with a unique core
compatible with BTD (Lᵣ,Lᵣ, 1) results in BTDCORCONDIA values of ∼ 100%. In contrast,
incompatible data will lead to low values. The result confirms that it is possible to perform a
core consistency diagnosis to check the compatibility between the model and data in BTD.
In summary, multimodal data fusion of paediatric brain data through matrix-tensor
decomposition offers a new approach to studying the shared underlying profiles and
developmental status of children with neurological diseases such as epilepsy. This could be
a stepping stone for future research seeking to integrate and adopt data fusion approaches
as additional tools for clinicians to prioritise children for an exhaustive assessment of their development.
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