scholarly journals Diagnosis of Alzheimer’s Disease Using Brain Network

2021 ◽  
Vol 15 ◽  
Author(s):  
Ramesh Kumar Lama ◽  
Goo-Rak Kwon

Recent studies suggest the brain functional connectivity impairment is the early event occurred in case of Alzheimer’s disease (AD) as well as mild cognitive impairment (MCI). We model the brain as a graph based network to study these impairment. In this paper, we present a new diagnosis approach using graph theory based features from functional magnetic resonance (fMR) images to discriminate AD, MCI, and healthy control (HC) subjects using different classification techniques. These techniques include linear support vector machine (LSVM), and regularized extreme learning machine (RELM). We used pairwise Pearson’s correlation-based functional connectivity to construct the brain network. We compare the classification performance of brain network using Alzheimer’s disease neuroimaging initiative (ADNI) datasets. Node2vec graph embedding approach is employed to convert graph features to feature vectors. Experimental results show that the SVM with LASSO feature selection method generates better classification accuracy compared to other classification technique.

2020 ◽  
Vol 10 (3) ◽  
pp. 667-671
Author(s):  
Jing Sun ◽  
Yanhui Ding ◽  
Kun Zhao ◽  
Haiyan Xu ◽  
Yongxin Zhang ◽  
...  

Alzheimer's disease (AD) is a progressive neurodegenerative disease. Right now there is no cure for AD. As we know, the brain structure is constantly changing as it progresses to AD. If we can detect these changes, it may be helpful to discover new biomarkers and early diagnosis of AD. We use the deep learning method DeepWalk to extract the structural features of each subject based on brain function connection. The method takes a brain topology network based on functional connection transformations as input and outputs a potential feature representation for each brain region in the brain network structure. In the current research, a new potential biomarker is found, which is based on a structural feature that can represent changes in brain connectivity. In our experiment, 79 Resting-state fMRI were used from ADNI dataset, including 49 normal controls (NCs) and 30 AD patients. By analyzing the structural features between AD patients and NCs, obvious differences are detected in the temporal lobe, parietal lobe, and frontal lobe. We use a support vector machine (SVM) model to evaluate the performance of these structural features, and its classification performance achieves 80.36% accuracy (specificity = 73.67%, sensitivity = 87.17%). In general, these findings indicate that structural features may be a new potential biomarker between NCs and AD patients.


2020 ◽  
Vol 10 (3) ◽  
pp. 667-671
Author(s):  
Jing Sun ◽  
Yanhui Ding ◽  
Kun Zhao ◽  
Haiyan Xu ◽  
Yongxin Zhang ◽  
...  

Alzheimer's disease (AD) is a progressive neurodegenerative disease. Right now there is no cure for AD. As we know, the brain structure is constantly changing as it progresses to AD. If we can detect these changes, it may be helpful to discover new biomarkers and early diagnosis of AD. We use the deep learning method DeepWalk to extract the structural features of each subject based on brain function connection. The method takes a brain topology network based on functional connection transformations as input and outputs a potential feature representation for each brain region in the brain network structure. In the current research, a new potential biomarker is found, which is based on a structural feature that can represent changes in brain connectivity. In our experiment, 79 Resting-state fMRI were used from ADNI dataset, including 49 normal controls (NCs) and 30 AD patients. By analyzing the structural features between AD patients and NCs, obvious differences are detected in the temporal lobe, parietal lobe, and frontal lobe. We use a support vector machine (SVM) model to evaluate the performance of these structural features, and its classification performance achieves 80.36% accuracy (specificity = 73.67%, sensitivity = 87.17%). In general, these findings indicate that structural features may be a new potential biomarker between NCs and AD patients.


2020 ◽  
Vol 14 ◽  
Author(s):  
Ali Noroozi ◽  
Mansoor Rezghi

Recently, machine learning methods have gained lots of attention from researchers seeking to analyze brain images such as Resting-State Functional Magnetic Resonance Imaging (rs-fMRI) to obtain a deeper understanding of the brain and such related diseases, for example, Alzheimer's disease. Finding the common patterns caused by a brain disorder through analysis of the functional connectivity (FC) network along with discriminating brain diseases from normal controls have long been the two principal goals in studying rs-fMRI data. The majority of FC extraction methods calculate the FC matrix for each subject and then use simple techniques to combine them and obtain a general FC matrix. In addition, the state-of-the-art classification techniques for finding subjects with brain disorders also rely on calculating an FC for each subject, vectorizing, and feeding them to the classifier. Considering these problems and based on multi-dimensional nature of the data, we have come up with a novel tensor framework in which a general FC matrix is obtained without the need to construct an FC matrix for each sample. This framework also allows us to reduce the dimensionality and create a novel discriminant function that rather than using FCs works directly with each sample, avoids vectorization in any step, and uses the test data in the training process without forcing any prior knowledge of its label into the classifier. Extensive experiments using the ADNI dataset demonstrate that our proposed framework effectively boosts the fMRI classification performance and reveals novel connectivity patterns in Alzheimer's disease at its early stages.


2021 ◽  
Vol 15 ◽  
Author(s):  
Justine Staal ◽  
Francesco Mattace-Raso ◽  
Hennie A. M. Daniels ◽  
Johannes van der Steen ◽  
Johan J. M. Pel

BackgroundResearch into Alzheimer’s disease has shifted toward the identification of minimally invasive and less time-consuming modalities to define preclinical stages of Alzheimer’s disease.MethodHere, we propose visuomotor network dysfunctions as a potential biomarker in AD and its prodromal stage, mild cognitive impairment with underlying the Alzheimer’s disease pathology. The functionality of this network was tested in terms of timing, accuracy, and speed with goal-directed eye-hand tasks. The predictive power was determined by comparing the classification performance of a zero-rule algorithm (baseline), a decision tree, a support vector machine, and a neural network using functional parameters to classify controls without cognitive disorders, mild cognitive impaired patients, and Alzheimer’s disease patients.ResultsFair to good classification was achieved between controls and patients, controls and mild cognitive impaired patients, and between controls and Alzheimer’s disease patients with the support vector machine (77–82% accuracy, 57–93% sensitivity, 63–90% specificity, 0.74–0.78 area under the curve). Classification between mild cognitive impaired patients and Alzheimer’s disease patients was poor, as no algorithm outperformed the baseline (63% accuracy, 0% sensitivity, 100% specificity, 0.50 area under the curve).Comparison with Existing Method(s)The classification performance found in the present study is comparable to that of the existing CSF and MRI biomarkers.ConclusionThe data suggest that visuomotor network dysfunctions have potential in biomarker research and the proposed eye-hand tasks could add to existing tests to form a clear definition of the preclinical phenotype of AD.


2021 ◽  
Author(s):  
Hessam Ahmadi ◽  
Emad Fatemizadeh ◽  
Ali Motie Nasrabadi

Abstract Neuroimaging data analysis reveals the underlying interactions in the brain. It is essential, yet controversial, to choose a proper tool to manifest brain functional connectivity. In this regard, researchers have not reached a definitive conclusion between the linear and non-linear approaches, as both have pros and cons. In this study, to evaluate this concern, the functional Magnetic Resonance Imaging (fMRI) data of different stages of Alzheimer’s disease are investigated. In the linear approach, the Pearson Correlation Coefficient (PCC) is employed as a common technique to generate brain functional graphs. On the other hand, for non-linear approaches, two methods including Distance Correlation (DC) and the kernel trick are utilized. By the use of the three mentioned routines and graph theory, functional brain networks of all stages of Alzheimer’s disease (AD) are constructed and then sparsed. Afterwards, graph global measures are calculated over the networks and a non-parametric permutation test is conducted. Results reveal that the non-linear approaches have more potential to discriminate groups in all stages of AD. Moreover, the kernel trick method is more powerful in comparison to the DC technique. Nevertheless, AD degenerates the brain functional graphs more at the beginning stages of the disease. At the first phase, both functional integration and segregation of the brain degrades, and as AD progressed brain functional segregation further declines. The most distinguishable feature in all stages is the clustering coefficient that reflects brain functional segregation.


Author(s):  
A. Thushara ◽  
C. Ushadevi Amma ◽  
Ansamma John

Alzheimer’s Disease (AD) is basically a progressive neurodegenerative disorder associated with abnormal brain networks that affect millions of elderly people and degrades their quality of life. The abnormalities in brain networks are due to the disruption of White Matter (WM) fiber tracts that connect the brain regions. Diffusion-Weighted Imaging (DWI) captures the brain’s WM integrity. Here, the correlation betwixt the WM degeneration and also AD is investigated by utilizing graph theory as well as Machine Learning (ML) algorithms. By using the DW image obtained from Alzheimer’s Disease Neuroimaging Initiative (ADNI) database, the brain graph of each subject is constructed. The features extracted from the brain graph form the basis to differentiate between Mild Cognitive Impairment (MCI), Control Normal (CN) and AD subjects. Performance evaluation is done using binary and multiclass classification algorithms and obtained an accuracy that outperforms the current top-notch DWI-based studies.


Entropy ◽  
2019 ◽  
Vol 21 (3) ◽  
pp. 300 ◽  
Author(s):  
Shuaizong Si ◽  
Bin Wang ◽  
Xiao Liu ◽  
Chong Yu ◽  
Chao Ding ◽  
...  

Alzheimer’s disease (AD) is a progressive disease that causes problems of cognitive and memory functions decline. Patients with AD usually lose their ability to manage their daily life. Exploring the progression of the brain from normal controls (NC) to AD is an essential part of human research. Although connection changes have been found in the progression, the connection mechanism that drives these changes remains incompletely understood. The purpose of this study is to explore the connection changes in brain networks in the process from NC to AD, and uncovers the underlying connection mechanism that shapes the topologies of AD brain networks. In particular, we propose a mutual information brain network model (MINM) from the perspective of graph theory to achieve our aim. MINM concerns the question of estimating the connection probability between two cortical regions with the consideration of both the mutual information of their observed network topologies and their Euclidean distance in anatomical space. In addition, MINM considers establishing and deleting connections, simultaneously, during the networks modeling from the stage of NC to AD. Experiments show that MINM is sufficient to capture an impressive range of topological properties of real brain networks such as characteristic path length, network efficiency, and transitivity, and it also provides an excellent fit to the real brain networks in degree distribution compared to experiential models. Thus, we anticipate that MINM may explain the connection mechanism for the formation of the brain network organization in AD patients.


Author(s):  
Bhuvaneshwari Bhaskaran ◽  
Kavitha Anandan

Alzheimer's disease (AD) is a progressive brain disorder which has a long preclinical phase. The beta-amyloid plaques and tangles in the brain are considered as the main pathological causes. Functional connectivity is typically examined in capturing brain network dynamics in AD. A definitive underconnectivity is observed in patients through the progressive stages of AD. Graph theoretic modeling approaches have been effective in understanding the brain dynamics. In this article, the brain connectivity patterns and the functional topology through the progression of Alzheimer's disease are analysed using resting state fMRI. The altered network topology is analysed by graphed theoretical measures and explains cognitive deficits caused by the progression of this disease. Results show that the functional topology is disrupted in the default mode network regions as the disease progresses in patients. Further, it is observed that there is a lack of left lateralization involving default mode network regions as the severity in AD increases.


2020 ◽  
Vol 10 (2) ◽  
pp. 370-379 ◽  
Author(s):  
Jie Cai ◽  
Lingjing Hu ◽  
Zhou Liu ◽  
Ke Zhou ◽  
Huailing Zhang

Background: Mild cognitive impairment (MCI) patients are a high-risk group for Alzheimer's disease (AD). Each year, the diagnosed of 10–15% of MCI patients are converted to AD (MCI converters, MCI_C), while some MCI patients remain relatively stable, and unconverted (MCI stable, MCI_S). MCI patients are considered the most suitable population for early intervention treatment for dementia, and magnetic resonance imaging (MRI) is clinically the most recommended means of imaging examination. Therefore, using MRI image features to reliably predict the conversion from MCI to AD can help physicians carry out an effective treatment plan for patients in advance so to prevent or slow down the development of dementia. Methods: We proposed an embedded feature selection method based on the least squares loss function and within-class scatter to select the optimal feature subset. The optimal subsets of features were used for binary classification (AD, MCI_C, MCI_S, normal control (NC) in pairs) based on a support vector machine (SVM), and the optimal 3-class features were used for 3-class classification (AD, MCI_C, MCI_S, NC in triples) based on one-versus-one SVMs (OVOSVMs). To ensure the insensitivity of the results to the random train/test division, a 10-fold cross-validation has been repeated for each classification. Results: Using our method for feature selection, only 7 features were selected from the original 90 features. With using the optimal subset in the SVM, we classified MCI_C from MCI_S with an accuracy, sensitivity, and specificity of 71.17%, 68.33% and 73.97%, respectively. In comparison, in the 3-class classification (AD vs. MCI_C vs. MCI_S) with OVOSVMs, our method selected 24 features, and the classification accuracy was 81.9%. The feature selection results were verified to be identical to the conclusions of the clinical diagnosis. Our feature selection method achieved the best performance, comparing with the existing methods using lasso and fused lasso for feature selection. Conclusion: The results of this study demonstrate the potential of the proposed approach for predicting the conversion from MCI to AD by identifying the affected brain regions undergoing this conversion.


2018 ◽  
Vol 28 (09) ◽  
pp. 1850022 ◽  
Author(s):  
Olga Valenzuela ◽  
Xiaoyi Jiang ◽  
Antonio Carrillo ◽  
Ignacio Rojas

Computer-Aided Diagnosis (CAD) represents a relevant instrument to automatically classify between patients with and without Alzheimer's Disease (AD) using several actual imaging techniques. This study analyzes the optimization of volumes of interest (VOIs) to extract three-dimensional (3D) textures from Magnetic Resonance Image (MRI) in order to diagnose AD, Mild Cognitive Impairment converter (MCIc), Mild Cognitive Impairment nonconverter (MCInc) and Normal subjects. A relevant feature of the proposed approach is the use of 3D features instead of traditional two-dimensional (2D) features, by using 3D discrete wavelet transform (3D-DWT) approach for performing feature extraction from T-1 weighted MRI. Due to the high number of coefficients when applying 3D-DWT to each of the VOIs, a feature selection algorithm based on mutual information is used, as is the minimum Redundancy Maximum Relevance (mRMR) algorithm. Region optimization has been performed in order to discover the most relevant regions (VOIs) in the brain with the use of Multi-Objective Genetic Algorithms, being one of the objectives to be optimize the accuracy of the system. The error index of the system is computed by the confusion matrix obtained by the multi-class support vector machine (SVM) classifier. Principal Component Analysis (PCA) is used with the purpose of reducing the number of features to the classifier. The cohort of subjects used in the study consisted of 296 different patients. A first group of 206 patients was used to optimize VOI selection and another group of 90 independent subjects (that did not belong to the first group) was used to test the solutions yielded by the genetic algorithm. The proposed methodology obtains excellent results in multi-class classification achieving accuracies of 94.4% and also extracting significant information on the location of the most relevant points of the brain. This suggests that the proposed method could aid in the research of other neurodegenerative diseases, improving the accuracy of the diagnosis and finding the most relevant regions of the brain associated with them.


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