4.5 Article

Identifying brain regions contributing to Alzheimer's disease using self regulating particle swarm optimization

Journal

Publisher

WILEY
DOI: 10.1002/ima.22458

Keywords

Alzheimer's disease; gray matter; magnetic resonance imaging; particle swarm optimization; support vector machines; white matter

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This article introduced a method to detect brain regions involved in Alzheimer's disease using SVM classifiers and SRPSO algorithm, achieving better classification performance by integrating GM and WM features and incorporating clinical features. The use of SRPSO for feature extraction helped identify important brain regions for AD versus CN classification.
In this article, we developed an approach for detecting brain regions that contribute to Alzheimer's disease (AD) using support vector machine (SVM) classifiers and the recently developed self regulating particle swarm optimization (SRPSO) algorithm. SRPSO employs strategies inspired by the principles of learning in humans to achieve faster and better optimization results. The classifiers for distinguishing subjects into AD patients and cognitively normal (CN) individuals were built using grey matter (GM) and white matter (WM) volumetric features extracted from structural magnetic resonance (MR) images. It could be observed from results that the classifier built using both GM and WM features provided accuracy of 89.26% which is better than the performance of classifiers built using either GM or WM features only. Moreover, consideration of clinical features in addition to volumetric features improves the accuracy further to 94.63% which is better than the performance reported by recent works in literature. In order to identify the brain regions that are important for AD vs CN classification problem, we used SRPSO to extract GM and WM features that yield better classification performance. Using 50 features identified by SRPSO, an accuracy of 89.39% was obtained which is close to the accuracy based on all features. The features identified by SRPSO were mapped back to the brain to identify brain regions that exhibit degeneration in AD. In addition to identifying areas known to be involved in AD like cerebellum, hippocampus, this helped in finding newer areas that might contribute towards AD.

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