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Study of Tissue Variation and Analysis of MR Brain Images using Optimized Multilevel Threshold and Deep CNN Features in Neurodegenerative Disorders

机译:优化的多级阈值和神经退行性疾病的深CNN特征对MR脑图像的组织变异和分析的研究

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Dementia is a degenerative irreversible disorder that globally causes a high socio-economic burden. The pathology progression of mild cognitive impairment (MCI) and Alzheimer diseases (AD) are correlated with each other. There is a need to examine the pathology variation to discriminate the disorder to provide appropriate treatment strategies. This study investigates about the brain tissue variations to identify the subtle change in progression. The considered normal, MCI and AD magnetic resonance (MR) images are obtained from Alzheimer’s disease Neuroimaging Initiative (ADNI). In this work, multilevel Tsallis based grey wolf optimization (GWO) is used to segment the brain tissues. Then the feature is extracted from segmented white matter (WM), grey matter (GM) and cerebro spinal fluid (CSF) using convolution neural network (CNN). The obtained deep features are given to principal component analysis (PCA) to obtain a prominent feature set for normal, MCI and AD. Further the tissue variation of optimized deep features is analyzed using support vector machine (SVM). The results shows that Tsallis based GWO perform reliable tissue segmentation for normal, MCI and AD. The deep features are able to observe discrimination than the fully considered feature set. Finally, the classifier result shows distinct tissue variation among normal, MCI and AD subjects. Further the prominent features give a classification accuracy of 77%, 80.22% and 78.7% for WM, GM and CSF respectively. This concludes that GM variation is a close biological substrate of dementia progressive condition than the effects of time or aging. Thus, the proposed framework can be used as an effective system for diagnosis of progression in neurodegenerative disorders.
机译:痴呆症是一种不可逆性的退化性疾病,在全球范围内造成很高的社会经济负担。轻度认知障碍(MCI)和阿尔茨海默氏病(AD)的病理进展相互关联。需要检查病理变化以区分疾病以提供适当的治疗策略。这项研究调查了大脑组织的变化,以确定进展中的细微变化。认为正常的MCI和AD磁共振(MR)图像是从阿尔茨海默氏病神经成像计划(ADNI)获得的。在这项工作中,基于多级Tsallis的灰狼优化(GWO)用于分割大脑组织。然后使用卷积神经网络(CNN)从分割的白质(WM),灰质(GM)和脑脊髓液(CSF)中提取特征。将获得的深层特征进行主成分分析(PCA),以获得正常,MCI和AD的显着特征集。此外,使用支持向量机(SVM)分析优化后的深部特征的组织变化。结果表明,基于Tsallis的GWO对正常,MCI和AD执行可靠的组织分割。与完全考虑的功能集相比,深层功能能够观察到歧视。最后,分类器结果显示正常,MCI和AD受试者之间明显的组织变异。此外,WM,GM和CSF的突出特征分别提供77%,80.22%和78.7%的分类精度。得出的结论是,与时间或衰老的影响相比,GM变异是痴呆症进行性疾病的紧密生物学底物。因此,提出的框架可以用作诊断神经退行性疾病进展的有效系统。

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