Classifying Alzheimer's Disease Using a Finite Basis Physics Neural Network

ABSTRACT The disease amyloid plaques, neurofibrillary tangles, synaptic dysfunction, and neuronal death gradually accumulate throughout Alzheimer's disease (AD), resulting in cognitive decline and functional disability. The challenges of dataset quality, interpretability, ethical integration, p...

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Published inMicroscopy research and technique Vol. 88; no. 4; pp. 1115 - 1127
Main Authors Dhavamani, Logeshwari, Joshi, Sagar Vasantrao, Kothapalli, Pavan Kumar Varma, Elangovan, Muniyandy, Putchanuthala, Ramesh Babu, Senthamil Selvan, Ramasamy
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.04.2025
Wiley Subscription Services, Inc
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ISSN1059-910X
1097-0029
1097-0029
DOI10.1002/jemt.24727

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Abstract ABSTRACT The disease amyloid plaques, neurofibrillary tangles, synaptic dysfunction, and neuronal death gradually accumulate throughout Alzheimer's disease (AD), resulting in cognitive decline and functional disability. The challenges of dataset quality, interpretability, ethical integration, population variety, and picture standardization must be addressed using deep learning for the functional magnetic resonance imaging (MRI) classification of AD in order to guarantee a trustworthy and practical therapeutic application. In this manuscript Classifying AD using a finite basis physics neural network (CAD‐FBPINN) is proposed. Initially, images are collected from AD Neuroimaging Initiative (ADNI) dataset. The images are fed to Pre‐processing segment. During the preprocessing phase the reverse lognormal Kalman filter (RLKF) is used to enhance the input images. Then the preprocessed images are given to the feature extraction process. Feature extraction is done by Newton‐time‐extracting wavelet transform (NTEWT), which is used to extract the statistical features such as the mean, kurtosis, and skewness. Finally the features extracted are given to FBPINNs for Classifying AD such as early mild cognitive impairment (EMCI), AD, mild cognitive impairment (MCI), late mild cognitive impairment (LMCI), normal control (NC), and subjective memory complaints (SMCs). In General, FBPINN does not express adapting optimization strategies to determine optimal factors to ensure correct AD classification. Hence, sea‐horse optimization algorithm (SHOA) to optimize FBPINN, which accurately classifies AD. The proposed technique implemented in python and efficacy of the CAD‐FBPINN technique is assessed with support of numerous performances like accuracy, precision, Recall, F1‐score, specificity and negative predictive value (NPV) is analyzed. Proposed CAD‐FBPINN method attain 30.53%, 23.34%, and 32.64% higher accuracy; 20.53%, 25.34%, and 29.64% higher precision; 20.53%, 25.34%, and 29.64% higher NP values analyzed with the existing for Classifying AD Stages through Brain Modifications using FBPINNs Optimized with sea‐horse optimizer. Then, the effectiveness of the CAD‐FBPINN technique is compared to other methods that are currently in use, such as AD diagnosis and classification using a convolution neural network algorithm (DC‐AD‐AlexNet), Predicting diagnosis 4 years before Alzheimer's disease incident (PDP‐ADI‐GCNN), and Using the DC‐AD‐AlexNet convolution neural network algorithm, diagnose and classify AD. For Alzheimer's disease (AD) classification, MRI images from the ADNI dataset are first preprocessed using a reverse lognormal Kalman filter (RLKF) to enhance image quality. Key statistical features are then extracted with the Newton‐time‐extracting wavelet transform (NTEWT). A finite basis physics‐informed neural network (FBPINN), optimized with the sea‐horse optimization algorithm (SHOA), is employed for classifying AD stages. This approach effectively classifies stages including EMCI, AD, MCI, LMCI, NC, and SMC.
AbstractList The disease amyloid plaques, neurofibrillary tangles, synaptic dysfunction, and neuronal death gradually accumulate throughout Alzheimer's disease (AD), resulting in cognitive decline and functional disability. The challenges of dataset quality, interpretability, ethical integration, population variety, and picture standardization must be addressed using deep learning for the functional magnetic resonance imaging (MRI) classification of AD in order to guarantee a trustworthy and practical therapeutic application. In this manuscript Classifying AD using a finite basis physics neural network (CAD‐FBPINN) is proposed. Initially, images are collected from AD Neuroimaging Initiative (ADNI) dataset. The images are fed to Pre‐processing segment. During the preprocessing phase the reverse lognormal Kalman filter (RLKF) is used to enhance the input images. Then the preprocessed images are given to the feature extraction process. Feature extraction is done by Newton‐time‐extracting wavelet transform (NTEWT), which is used to extract the statistical features such as the mean, kurtosis, and skewness. Finally the features extracted are given to FBPINNs for Classifying AD such as early mild cognitive impairment (EMCI), AD, mild cognitive impairment (MCI), late mild cognitive impairment (LMCI), normal control (NC), and subjective memory complaints (SMCs). In General, FBPINN does not express adapting optimization strategies to determine optimal factors to ensure correct AD classification. Hence, sea‐horse optimization algorithm (SHOA) to optimize FBPINN, which accurately classifies AD. The proposed technique implemented in python and efficacy of the CAD‐FBPINN technique is assessed with support of numerous performances like accuracy, precision, Recall, F1‐score, specificity and negative predictive value (NPV) is analyzed. Proposed CAD‐FBPINN method attain 30.53%, 23.34%, and 32.64% higher accuracy; 20.53%, 25.34%, and 29.64% higher precision; 20.53%, 25.34%, and 29.64% higher NP values analyzed with the existing for Classifying AD Stages through Brain Modifications using FBPINNs Optimized with sea‐horse optimizer. Then, the effectiveness of the CAD‐FBPINN technique is compared to other methods that are currently in use, such as AD diagnosis and classification using a convolution neural network algorithm (DC‐AD‐AlexNet), Predicting diagnosis 4 years before Alzheimer's disease incident (PDP‐ADI‐GCNN), and Using the DC‐AD‐AlexNet convolution neural network algorithm, diagnose and classify AD.
ABSTRACT The disease amyloid plaques, neurofibrillary tangles, synaptic dysfunction, and neuronal death gradually accumulate throughout Alzheimer's disease (AD), resulting in cognitive decline and functional disability. The challenges of dataset quality, interpretability, ethical integration, population variety, and picture standardization must be addressed using deep learning for the functional magnetic resonance imaging (MRI) classification of AD in order to guarantee a trustworthy and practical therapeutic application. In this manuscript Classifying AD using a finite basis physics neural network (CAD‐FBPINN) is proposed. Initially, images are collected from AD Neuroimaging Initiative (ADNI) dataset. The images are fed to Pre‐processing segment. During the preprocessing phase the reverse lognormal Kalman filter (RLKF) is used to enhance the input images. Then the preprocessed images are given to the feature extraction process. Feature extraction is done by Newton‐time‐extracting wavelet transform (NTEWT), which is used to extract the statistical features such as the mean, kurtosis, and skewness. Finally the features extracted are given to FBPINNs for Classifying AD such as early mild cognitive impairment (EMCI), AD, mild cognitive impairment (MCI), late mild cognitive impairment (LMCI), normal control (NC), and subjective memory complaints (SMCs). In General, FBPINN does not express adapting optimization strategies to determine optimal factors to ensure correct AD classification. Hence, sea‐horse optimization algorithm (SHOA) to optimize FBPINN, which accurately classifies AD. The proposed technique implemented in python and efficacy of the CAD‐FBPINN technique is assessed with support of numerous performances like accuracy, precision, Recall, F1‐score, specificity and negative predictive value (NPV) is analyzed. Proposed CAD‐FBPINN method attain 30.53%, 23.34%, and 32.64% higher accuracy; 20.53%, 25.34%, and 29.64% higher precision; 20.53%, 25.34%, and 29.64% higher NP values analyzed with the existing for Classifying AD Stages through Brain Modifications using FBPINNs Optimized with sea‐horse optimizer. Then, the effectiveness of the CAD‐FBPINN technique is compared to other methods that are currently in use, such as AD diagnosis and classification using a convolution neural network algorithm (DC‐AD‐AlexNet), Predicting diagnosis 4 years before Alzheimer's disease incident (PDP‐ADI‐GCNN), and Using the DC‐AD‐AlexNet convolution neural network algorithm, diagnose and classify AD. For Alzheimer's disease (AD) classification, MRI images from the ADNI dataset are first preprocessed using a reverse lognormal Kalman filter (RLKF) to enhance image quality. Key statistical features are then extracted with the Newton‐time‐extracting wavelet transform (NTEWT). A finite basis physics‐informed neural network (FBPINN), optimized with the sea‐horse optimization algorithm (SHOA), is employed for classifying AD stages. This approach effectively classifies stages including EMCI, AD, MCI, LMCI, NC, and SMC.
The disease amyloid plaques, neurofibrillary tangles, synaptic dysfunction, and neuronal death gradually accumulate throughout Alzheimer's disease (AD), resulting in cognitive decline and functional disability. The challenges of dataset quality, interpretability, ethical integration, population variety, and picture standardization must be addressed using deep learning for the functional magnetic resonance imaging (MRI) classification of AD in order to guarantee a trustworthy and practical therapeutic application. In this manuscript Classifying AD using a finite basis physics neural network (CAD-FBPINN) is proposed. Initially, images are collected from AD Neuroimaging Initiative (ADNI) dataset. The images are fed to Pre-processing segment. During the preprocessing phase the reverse lognormal Kalman filter (RLKF) is used to enhance the input images. Then the preprocessed images are given to the feature extraction process. Feature extraction is done by Newton-time-extracting wavelet transform (NTEWT), which is used to extract the statistical features such as the mean, kurtosis, and skewness. Finally the features extracted are given to FBPINNs for Classifying AD such as early mild cognitive impairment (EMCI), AD, mild cognitive impairment (MCI), late mild cognitive impairment (LMCI), normal control (NC), and subjective memory complaints (SMCs). In General, FBPINN does not express adapting optimization strategies to determine optimal factors to ensure correct AD classification. Hence, sea-horse optimization algorithm (SHOA) to optimize FBPINN, which accurately classifies AD. The proposed technique implemented in python and efficacy of the CAD-FBPINN technique is assessed with support of numerous performances like accuracy, precision, Recall, F1-score, specificity and negative predictive value (NPV) is analyzed. Proposed CAD-FBPINN method attain 30.53%, 23.34%, and 32.64% higher accuracy; 20.53%, 25.34%, and 29.64% higher precision; 20.53%, 25.34%, and 29.64% higher NP values analyzed with the existing for Classifying AD Stages through Brain Modifications using FBPINNs Optimized with sea-horse optimizer. Then, the effectiveness of the CAD-FBPINN technique is compared to other methods that are currently in use, such as AD diagnosis and classification using a convolution neural network algorithm (DC-AD-AlexNet), Predicting diagnosis 4 years before Alzheimer's disease incident (PDP-ADI-GCNN), and Using the DC-AD-AlexNet convolution neural network algorithm, diagnose and classify AD.The disease amyloid plaques, neurofibrillary tangles, synaptic dysfunction, and neuronal death gradually accumulate throughout Alzheimer's disease (AD), resulting in cognitive decline and functional disability. The challenges of dataset quality, interpretability, ethical integration, population variety, and picture standardization must be addressed using deep learning for the functional magnetic resonance imaging (MRI) classification of AD in order to guarantee a trustworthy and practical therapeutic application. In this manuscript Classifying AD using a finite basis physics neural network (CAD-FBPINN) is proposed. Initially, images are collected from AD Neuroimaging Initiative (ADNI) dataset. The images are fed to Pre-processing segment. During the preprocessing phase the reverse lognormal Kalman filter (RLKF) is used to enhance the input images. Then the preprocessed images are given to the feature extraction process. Feature extraction is done by Newton-time-extracting wavelet transform (NTEWT), which is used to extract the statistical features such as the mean, kurtosis, and skewness. Finally the features extracted are given to FBPINNs for Classifying AD such as early mild cognitive impairment (EMCI), AD, mild cognitive impairment (MCI), late mild cognitive impairment (LMCI), normal control (NC), and subjective memory complaints (SMCs). In General, FBPINN does not express adapting optimization strategies to determine optimal factors to ensure correct AD classification. Hence, sea-horse optimization algorithm (SHOA) to optimize FBPINN, which accurately classifies AD. The proposed technique implemented in python and efficacy of the CAD-FBPINN technique is assessed with support of numerous performances like accuracy, precision, Recall, F1-score, specificity and negative predictive value (NPV) is analyzed. Proposed CAD-FBPINN method attain 30.53%, 23.34%, and 32.64% higher accuracy; 20.53%, 25.34%, and 29.64% higher precision; 20.53%, 25.34%, and 29.64% higher NP values analyzed with the existing for Classifying AD Stages through Brain Modifications using FBPINNs Optimized with sea-horse optimizer. Then, the effectiveness of the CAD-FBPINN technique is compared to other methods that are currently in use, such as AD diagnosis and classification using a convolution neural network algorithm (DC-AD-AlexNet), Predicting diagnosis 4 years before Alzheimer's disease incident (PDP-ADI-GCNN), and Using the DC-AD-AlexNet convolution neural network algorithm, diagnose and classify AD.
Author Joshi, Sagar Vasantrao
Putchanuthala, Ramesh Babu
Dhavamani, Logeshwari
Senthamil Selvan, Ramasamy
Elangovan, Muniyandy
Kothapalli, Pavan Kumar Varma
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Keywords sea‐horse optimization algorithm
finite basis physics‐informed neural networks
reverse lognormal Kalman filter
Newton‐time‐extracting wavelet transform
Alzheimer's disease
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Snippet ABSTRACT The disease amyloid plaques, neurofibrillary tangles, synaptic dysfunction, and neuronal death gradually accumulate throughout Alzheimer's disease...
The disease amyloid plaques, neurofibrillary tangles, synaptic dysfunction, and neuronal death gradually accumulate throughout Alzheimer's disease (AD),...
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SubjectTerms Algorithms
Alzheimer Disease - classification
Alzheimer Disease - diagnosis
Alzheimer Disease - diagnostic imaging
Alzheimer's disease
Amyloid
Artificial neural networks
Brain - diagnostic imaging
Brain - pathology
Classification
Cognitive ability
Cognitive Dysfunction - classification
Cognitive Dysfunction - diagnostic imaging
Convolution
Datasets
Deep Learning
Diagnosis
Effectiveness
Ethical standards
Feature extraction
finite basis physics‐informed neural networks
Functional magnetic resonance imaging
Horses
Humans
Image Processing, Computer-Assisted - methods
Impairment
Kalman filters
Kurtosis
Machine learning
Magnetic resonance imaging
Magnetic Resonance Imaging - methods
Medical imaging
Neural networks
Neural Networks, Computer
Neurodegenerative diseases
Neurofibrillary tangles
Neuroimaging
Neuroimaging - methods
Newton‐time‐extracting wavelet transform
Optimization
Physics
reverse lognormal Kalman filter
sea‐horse optimization algorithm
Senile plaques
Wavelet transforms
Title Classifying Alzheimer's Disease Using a Finite Basis Physics Neural Network
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjemt.24727
https://www.ncbi.nlm.nih.gov/pubmed/39704389
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https://www.proquest.com/docview/3147486929
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