Abstract

Alzheimer's disease (AD) is the kind of dementia that affects the most people around the world. Therefore, an early identification supporting effective treatments is required to increase the life quality of a wide number of patients. Recently, computer-aided diagnosis tools for dementia using Magnetic Resonance Imaging scans have been successfully proposed to discriminate between patients with AD, mild cognitive impairment, and healthy controls. Most of the attention has been given to the clinical data, provided by initiatives as the ADNI, supporting reliable researches on intervention, prevention, and treatments of AD. Therefore, there is a need for improving the performance of classification machines. In this paper, we propose a kernel framework for learning metrics that enhances conventional machines and supports the diagnosis of dementia. Our framework aims at building discriminative spaces through the maximization of center kernel alignment function, aiming at improving the discrimination of the three considered neurological classes. The proposed metric learning performance is evaluated on the widely-known ADNI database using three supervised classification machines (k-nn, SVM and NNs) for multi-class and bi-class scenarios from structural MRIs. Specifically, from ADNI collection 286 AD patients, 379 MCI patients and 231 healthy controls are used for development and validation of our proposed metric learning framework. For the experimental validation, we split the data into two subsets: 30% of subjects used like a blindfolded assessment and 70% employed for parameter tuning. Then, in the preprocessing stage, each structural MRI scan a total of 310 morphological measurements are automatically extracted from by FreeSurfer software package and concatenated to build an input feature matrix. Obtained test performance results, show that including a supervised metric learning improves the compared baseline classifiers in both scenarios. In the multi-class scenario, we achieve the best performance (accuracy 60.1%) for pretrained 1-layered NN, and we obtain measures over 90% in the average for HC vs. AD task. From the machine learning point of view, our proposal enhances the classifier performance by building spaces with a better class separability. From the clinical application, our enhancement results in a more balanced performance in each class than the compared approaches from the CADDementia challenge by increasing the sensitivity of pathological groups and the specificity of healthy controls.

Highlights

  • Alzheimer’s Disease (AD) corresponds to a progressive cognitive impairment and loss of memory functions, becoming the kind of dementia with the largest prevalence in elderly subjects with nearly 44 million patients worldwide

  • For enhancing the computer-aided diagnosis of dementia, we explore a metric learning framework based on the centered kernel alignment function, aiming to estimate more discriminative spaces

  • The proposed learning decodes discriminant information based on the maximization of the similarity between the input distribution and the corresponding target, aiming at enhancing the class separability

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Summary

Introduction

Alzheimer’s Disease (AD) corresponds to a progressive cognitive impairment and loss of memory functions, becoming the kind of dementia with the largest prevalence in elderly subjects with nearly 44 million patients worldwide. Dementia diagnosis and treatment demand reliable biomarkers providing an objective and early characterization of the different AD stages (Shi et al, 2015). Among these biomarkers, structural magnetic resonance imaging (MRI) data became frequently used to develop computer-aided diagnosis (CAD) tools due to its wide availability and non-invasiveness (Jack et al, 2013). CAD tools learn to discriminate dementia through MRI features, benefiting from large amounts of neuroimaging data. The Alzheimer’s Disease Neuroimaging Initiative (ADNI) focuses its researches on discriminating pathologies with a variety of classification tools from neuroimaging data, genetic information, and other biomarkes. Insufficient attention has been given to build appropriate metrics from the training data that could maximize the performance of several classifiers (Shi et al, 2015)

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