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ORIGINAL RESEARCH article

Front. Neuroinform.
Volume 18 - 2024 | doi: 10.3389/fninf.2024.1495571
This article is part of the Research Topic Neuro-detection: Advancements in Pattern Detection and Segmentation Techniques in Neuroscience View all 6 articles

Spectral Graph Convolutional Neural Network for Alzheimer Disease Diagnosis and Multi-Disease Categorization from Functional Brain Changes in Magnetic Resonance Images

Provisionally accepted
Hadeel Alharbi Hadeel Alharbi 1*Roben A. Juanita's Roben A. Juanita's 2Abdullah Al Hejaili Abdullah Al Hejaili 3Se-Jung Lim Se-Jung Lim 4
  • 1 University of Hail, Ha'il, Saudi Arabia
  • 2 National University, Manila, Philippines
  • 3 University of Tabuk, Tabuk, Tabuk, Saudi Arabia
  • 4 Chonnam National University, Gwangju, Gwangju, Republic of Korea

The final, formatted version of the article will be published soon.

    Alzheimer's Disease (AD) is a progressive neurological disorder characterized by the gradual deterioration of cognitive functions, leading to dementia and significantly impacting the quality of life for millions of people worldwide. Early and accurate diagnosis is crucial for the effective management and treatment of this debilitating condition. This study introduces a novel framework based on Spectral Graph Convolutional Neural Networks (SGCNN) for diagnosing AD and categorizing multiple diseases through the analysis of functional changes in brain structures captured via magnetic resonance imaging (MRI). To assess the effectiveness of our approach, we systematically analyze structural modifications to the SGCNN model through comprehensive ablation studies. The performance of various Convolutional Neural Networks (CNNs) is also evaluated, including SGCNN variants, Base CNN, Lean CNN, and Deep CNN. We begin with the original SGCNN model, which serves as our baseline and achieves a commendable classification accuracy of 93%. In our investigation, we perform two distinct ablation studies on the SGCNN model to examine how specific structural changes impact its performance. The results reveal that Ablation Model 1 significantly enhances accuracy, achieving an impressive 95%, while Ablation Model 2 maintains the baseline accuracy of 93%. Additionally, the Base CNN model demonstrates strong performance with a classification accuracy of 93%, whereas both the Lean CNN and Deep CNN models achieve 94% accuracy, indicating their competitive capabilities. To validate the models' effectiveness, we utilize multiple evaluation metrics, including accuracy, precision, recall, and F1-score, ensuring a thorough assessment of their performance. Our findings underscore that Ablation Model 1 (SGCNN Model 1) delivers the highest predictive accuracy among the tested models, highlighting its potential as a robust approach for Alzheimer's image classification. Ultimately, this research aims to facilitate early diagnosis and treatment of AD, contributing to improved patient outcomes and advancing the field of neurodegenerative disease diagnosis.

    Keywords: Alzheimer's disease (AD), image classification, Convolutional Neural Networks (CNN), SGCNN Model, deep learning, Ablation Study

    Received: 12 Sep 2024; Accepted: 14 Oct 2024.

    Copyright: © 2024 Alharbi, Juanita's, Al Hejaili and Lim. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Hadeel Alharbi, University of Hail, Ha'il, Saudi Arabia

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.