Deep Learning-Based Classification of Alzheimer’s Disease Using MRI Scans: A Customized Convolutional Neural Network Approach
Alzheimer's Disease (AD) is a complex condition impacting memory, cognition, and daily functions. Early diagnosis is crucial for effective management and treatment, although no cure currently exists. In this study, we develop and evaluate a custom Convolutional Neural Network (c-CNN) model for...
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Published in | SN computer science Vol. 5; no. 7; p. 917 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Singapore
Springer Nature Singapore
30.09.2024
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Alzheimer's Disease (AD) is a complex condition impacting memory, cognition, and daily functions. Early diagnosis is crucial for effective management and treatment, although no cure currently exists. In this study, we develop and evaluate a custom Convolutional Neural Network (c-CNN) model for AD classification using MRI scans. Our c-CNN model, featuring a unique architecture with two convolution layers, one max pooling layer, seven sequential layers, two dropout layers, and one dense output layer, is tested on three distinct MRI datasets. The first dataset comprises 6400 images categorized into four classes: Mild Demented (MiD), Moderate Demented (MdD), Non-Demented (ND), and Very Mild Demented (VMD). The second dataset includes 1296 images representing five stages of AD from the AD Neuroimaging Initiative (ADNI) repository. The third dataset contains 5154 images across three classes: AD, Confidence Interval (CI), and cognitive normal (CN). We rigorously compare our c-CNN model against DenseNet-121 (D-121), InceptionV3 (IV3), and Resnet 50 (Res-50) on these datasets. Our model outperforms others in accuracy, precision, recall, F1-score, area under the curve (AUC), and validation loss. These results underscore the effectiveness of our c-CNN model, highlighting its potential as a valuable tool for accurate AD classification. |
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ISSN: | 2661-8907 2662-995X 2661-8907 |
DOI: | 10.1007/s42979-024-03284-4 |