Background: Alzheimer’s disease (AD) is a common neurodegenerative disease occurring in the elderly population. The effective and accurate classification of AD symptoms by using functional magnetic resonance imaging (fMRI) has a great significance for the clinical diagnosis and prediction of AD patients. Methods: Therefore, this paper proposes a new method for identifying AD patients fromhealthy subjects by using functional connectivities (FCs) between the activity voxels in the brain based on fMRI data analysis. Firstly, independent component analysis is used to detect the activity voxels in the fMRI signals of AD patients and healthy subjects; Secondly, the FCs between the common activity voxels of the two groups are calculated, and then the FCs with significant differences are further identified by statistical analysis between them; Finally, the classification of AD patients fromhealthy subjects is realized by using FCs with significant differences as the feature samples in support vector machine. Results: The results show that the proposed identification method can obtain higher classification accuracy, and the FCs between activity voxels within prefrontal lobe as well as those between prefrontal and parietal lobes play an important role in the prediction of AD patients. Furthermore, we also find that more brain regions and much more voxels in some regions are activity in AD group compared with health control group. Conclusion: It has a great potential value for the AD pathogenesis mechanism study.

Granger causality (GC) is one of the most popular measures to investigate causality influence among brain regions and has been achieved significant results for exploring brain networks based on functional magnetic resonance imaging (fMRI). However, the predictors and order selection of conventional GC are based on linear models which result in such restrictions as poorly detection of nonlinearity and so on, in the application. This paper proposes a novel GC model called back propagation (BP) based kernel function Granger causality (BP_KFGC), in which symplectic geometry is used for embedding dimension and fuzzy inference system for predicting time series. The proposed method doesn’t depend on the prediction of the vector auto-regression model, so that time series don’t need to be wide-sense stationary as linear GC and kernel GC. In addition, it is a multivariate approach which is applicable to both linear and nonlinear systems and eliminates the effects of latent variables. The performance of the new method is evaluated and compared with linear GC, partial GC, neural network GC and kernel GC by simulated data with multiple adjustments to the nonlinearity. The results show that BP_KFGC outperforms the other four methods in detecting both linear and nonlinear causalities. Furthermore, we applied BP_KFGC to construct directed weight network (DWN) of Alzheimer's disease (AD) patients and health controls (HCs), and then nine graph-based features of DWN were used for classification by the classifier of support vector machine with radial basis kernel function. The accuracy of 95.89%, sensitivity of 93.31%, and specificity of 94.97% were achieved which may provide an auxiliary mean for the clinical diagnosis of AD.

Objective: The study of pathogenic mechanism at the genetic level by imaging genetics methods enables to effectively reveal the association of histopathology and genetics. However, there is a lack of effective and accurate tools to establish association models from macroscopic to microscopic. Methods: The multi-constrained joint non-negative matrix factorization (MCJNMF) was developed for simultaneous integration of genomic data and image data to identify common modules related to disease. Two types of data matrices were projected onto a common feature space, in which heterogeneous variables with large coefficients in the same projected direction form a common module. Meanwhile, the correlation between original data features was integrated by using regularization constraints to improve the biological relevance. Sparsity constraints and orthogonal constraints were performed on decomposition factors to minimize the redundancy between different bases and to reduce algorithm complexity. Results: This algorithm was successfully performed on the module identification of lung metastasis in soft tissue sarcomas (STSs) by integrating FDG-PET image and DNA methylation data features. Multilevel analysis on the top extracted modules revealed that these modules were closely related to the lung metastasis. Particularly, several genes with diagnostic potential for lung metastasis can be discovered from high score modules. Conclusion: This method not only can be applied for the accurate identification of patterns related to pathogenic mechanism of diseases, but also has a significant implication for discovering protein biomarkers. Significance: This method provides avenues for further studies of identifying complex association patterns of diseases according to different types of biological data.

Migraine seriously affects the physical and mental health of patients because of its recurrence and the hypersensitivity to the environment that it causes. However, the pathogenesis and pathophysiology of migraine are not fully understood. We addressed this issue in the present study using an autodynamic functional connectome model (A-DFCM) with twice-clustering to compare dynamic functional connectome patterns (DFCPs) from resting-state functional magnetic resonance imaging data from migraine patients and normal control subjects. We used automatic localization of segment points to improve the efficiency of the model, and intergroup differences and network metrics were analyzed to identify the neural mechanisms of migraine. Using the A-DFCM model, we identified 17 DFCPs—including 1 that was specific and 16 that were general—based on intergroup differences. The specific DFCP was closely associated with neuronal dysfunction in migraine, whereas the general DFCPs showed that the 2 groups had similar functional topology as well as differences in the brain resting state. An analysis of network metrics revealed the critical brain regions in the specific DFCP; these were not only distributed in brain areas related to pain such as Brodmann area 1/2/3, basal ganglia, and thalamus but also located in regions that have been implicated in migraine symptoms such as the occipital lobe. An analysis of the dissimilarities in general DFCPs between the 2 groups identified 6 brain areas belonging to the so-called pain matrix. Our findings provide insight into the neural mechanisms of migraine while also identifying neuroimaging biomarkers that can aid in the diagnosis or monitoring of migraine patients.

Judging and identifying biological activities and biomarkers inside tissues from imaging features of diseases is challenging, so correlating pathological image data with genes inside organisms is of great significance for clinical diagnosis. This paper proposes a high-dimensional kernel non-negative matrix factorization (NMF) method based on muti-modal information fusion. This algorithm can project RNA gene expression data and pathological images (WSI) into a common feature space, where the heterogeneous variables with the largest coefficient in the same projection direction form a co-module. In addition, the miRNA-mRNA and miRNA-lncRNA interaction networks in the ceRNA network are added to the algorithm as a priori information to explore the relationship between the images and the internal activities of the gene. Furthermore, the radial basis kernel function is used to calculate the feature proportion between different kinds of genes mapped in the high-dimensional feature space and projected into the common feature space to explore the gene interaction in the high-dimensional situation. The original feature matrix is regularized to improve biological correlation, and the feature factors are sparse by orthogonal constraints to reduce redundancy. Experimental results show that the proposed NMF method is better than the traditional NMF method in stability, decomposition accuracy, and robustness. Through data analysis applied to lung cancer, genes related to tissue morphology are found, such as COL7A1, CENPF and BIRC5. In addition, gene pairs with a correlation degree exceeding 0.8 are found, and potential biomarkers of significant correlation with survival are obtained such as CAPN8. It has potential application value for the clinical diagnosis of lung cancer.

Extracting massive features from images to quantify tumors provides a new insight to solve the problem that tumor heterogeneity is difficult to assess quantitatively. However, quantification of tumors by single-mode methods often has defects such as difficulty in features extraction and high computational complexity. The multimodal approach has shown effective application prospects in solving these problems. In this paper, we propose a feature fusion method based on positron emission tomography (PET) images and clinical information, which is used to obtain features for lung metastasis prediction of soft tissue sarcomas (STSs). Random forest method was adopted to select effective features by eliminating irrelevant or redundant features, and then they were used for the prediction of the lung metastasis combined with back propagation (BP) neural network. The results show that the prediction ability of the proposed model using fusion features is better than that of the model using an image or clinical feature alone. Furthermore, a good performance can be obtained using 3 standard uptake value (SUV) features of PET image and 7 clinical features, and its average accuracy, sensitivity, and specificity on all the sets can reach 92%, 91%, and 92%, respectively. Therefore, the fusing features have the potential to predict lung metastasis for STSs.