{"title":"Classifying Alzheimer's Disease Using a Finite Basis Physics Neural Network.","authors":"Logeshwari Dhavamani, Sagar Vasantrao Joshi, Pavan Kumar Varma Kothapalli, Muniyandy Elangovan, Ramesh Babu Putchanuthala, Ramasamy Senthamil Selvan","doi":"10.1002/jemt.24727","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":18684,"journal":{"name":"Microscopy Research and Technique","volume":" ","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microscopy Research and Technique","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/jemt.24727","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ANATOMY & MORPHOLOGY","Score":null,"Total":0}
引用次数: 0
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.
期刊介绍:
Microscopy Research and Technique (MRT) publishes articles on all aspects of advanced microscopy original architecture and methodologies with applications in the biological, clinical, chemical, and materials sciences. Original basic and applied research as well as technical papers dealing with the various subsets of microscopy are encouraged. MRT is the right form for those developing new microscopy methods or using the microscope to answer key questions in basic and applied research.