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

IF 2 3区 工程技术 Q2 ANATOMY & MORPHOLOGY
Logeshwari Dhavamani, Sagar Vasantrao Joshi, Pavan Kumar Varma Kothapalli, Muniyandy Elangovan, Ramesh Babu Putchanuthala, Ramasamy Senthamil Selvan
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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.

基于有限基物理神经网络的阿尔茨海默病分类。
淀粉样斑块、神经原纤维缠结、突触功能障碍和神经元死亡在阿尔茨海默病(AD)中逐渐累积,导致认知能力下降和功能障碍。使用深度学习进行AD的功能磁共振成像(MRI)分类,必须解决数据集质量、可解释性、伦理整合、人口多样性和图像标准化方面的挑战,以保证值得信赖和实际的治疗应用。本文提出了一种基于有限基物理神经网络(CAD-FBPINN)的AD分类方法。首先,图像收集自AD神经成像倡议(ADNI)数据集。将图像送入预处理段。在预处理阶段,使用反向对数正态卡尔曼滤波(RLKF)对输入图像进行增强。然后将预处理后的图像进行特征提取。特征提取由牛顿时间提取小波变换(NTEWT)完成,该小波变换用于提取均值、峰度和偏度等统计特征。最后将提取到的特征(早期轻度认知障碍(EMCI)、AD、轻度认知障碍(MCI)、晚期轻度认知障碍(LMCI)、正常对照(NC)和主观记忆抱怨(SMCs))提供给fbpinn进行AD分类。总的来说,FBPINN并没有表达自适应优化策略来确定最优因素以确保AD的正确分类。因此,采用海马优化算法(SHOA)对FBPINN进行优化,能够准确地对AD进行分类。该技术在python中实现,并在准确性、精密度、召回率、f1评分、特异性和阴性预测值(NPV)等众多性能的支持下评估CAD-FBPINN技术的有效性。CAD-FBPINN方法的准确率分别提高30.53%、23.34%和32.64%;精度分别提高20.53%、25.34%、29.64%;海马优化器优化后的fbpinn脑修饰对AD分期进行分类,与已有的NP值相比,分别高出20.53%、25.34%和29.64%。然后,将CAD-FBPINN技术与目前使用的卷积神经网络算法(DC-AD-AlexNet)、阿尔茨海默病发病前4年预测诊断(pdp - adii - gcnn)、使用DC-AD-AlexNet卷积神经网络算法对AD进行诊断和分类等方法的有效性进行比较。
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来源期刊
Microscopy Research and Technique
Microscopy Research and Technique 医学-解剖学与形态学
CiteScore
5.30
自引率
20.00%
发文量
233
审稿时长
4.7 months
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.
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