Major depressive disorder (MDD) may be driven by dysfunction in intrinsic dynamic properties of the brain, and EEG microstate is a promising method for analyzing brain dynamics. However, the alterations in EEG microstate is still not entirely clear, and its ability for MDDs detection is worth probing. Moreover, the mechanism behind the neural networks contributing to microstates remains poorly understood in MDDs. Therefore, we applied microstate analysis and Topographic Electrophysiological State Source-imaging (TESS) on EEG data of 27 MDDs and 28 healthy controls (HCs). Compared to HCs, MDDs had apparent increase in microstate C and decrease in microstate D. Furthermore, TESS results showed that the underlying network of microstate C in MDDs overlapped with the anterior cingulate cortex and left insula gyrus, whereas main source of microstate D was in the orbital part of inferior frontal gyrus. The reduced transition probability from C to D in MDDs may reveal an imbalance between the networks of microstates. The microstate parameters as features reached good performance in identifying MDD (89.09% accuracy, 92.86% sensitivity, 85.19% specificity), indicating their potential as biomarkers of depression pathology. Collectively, these results highlight alteration of brain activity patterns and provide new insights into abnormal EEG dynamics in MDDs.

At present, most brain functional studies are based on traditional frequency bands to explore the abnormal functional connections and topological organization of patients with depression. However, they ignore the characteristic relationship of electroencephalogram (EEG) signals in the time domain. Therefore, this paper proposes a network decomposition model based on Improved Empirical Mode Decomposition (EMD), it is suitable for time-frequency analysis of brain functional network. On the one hand, it solves the problem of mode mixing on original EMD method, especially on high-density EEG data. On the other hand, by building brain function networks on different intrinsic mode function (IMF), we can perform time-frequency analysis of brain function connections. It provides a new insight for brain function connectivity analysis of major depressive disorder (MDD). Experimental results found that the IMFs waveform decomposed by Improved EMD was more stable and the difference between IMFs was obvious, it indicated that the mode mixing can be effectively solved. Besides, the analysis of the brain network, we found that the changes in MDD functional connectivity on different IMFs, it may be related to the pathological changes for MDD. More statistical results on three network metrics proved that there were significant differences between MDD and normal controls (NC) group. In addition, the aberrant brain network structure of MDDs was also confirmed in the hubs characteristic. These findings may provide potential biomarkers for the clinical diagnosis of MDD patients.

Depression is a heterogeneous syndrome with certain individual differences among subjects. Exploring a feature selection method that can effectively mine the commonness intra-groups and the differences inter-groups in depression recognition is therefore of great significance. This study proposed a new clustering-fusion feature selection method. Hierarchical clustering (HC) algorithm was used to capture the heterogeneity distribution of subjects. Average and similarity network fusion (SNF) algorithms were adopted to characterize the brain network atlas of different populations. Differences analysis was also utilized to obtain the features with discriminant performance. Experiments showed that compared with traditional feature selection methods, HCSNF method yielded the optimal classification results of depression recognition in both sensor and source layers of electroencephalography (EEG) data. Especially in the beta band of EEG data at sensor layer, the classification performance was improved by more than 6%. Moreover, the long-distance connections between parietal-occipital lobe and other brain regions not only have high discriminative power, but also significantly correlate with depressive symptoms, indicating the important role of these features in depression recognition. Therefore, this study may provide methodological guidance for the discovery of reproducible electrophysiological biomarkers and new insights into common neuropathological mechanisms of heterogeneous depression diseases.

Objective. Brain connectivity network is a vital tool to reveal the interaction between different brain regions. Currently, most functional connectivity methods can only capture pairs of information to construct brain networks which ignored the high-order correlations between brain regions. Approach. Therefore, this study proposed a weighted connectivity hyper-network based on resting-state EEG data, and then applied to depression identification and analysis. The hyper-network model was build based on least absolute shrinkage and selection operator sparse regression method to effectively represent the higher-order relationships of brain regions. On this basis, by integrating the correlation-based weighted hyper-edge information, the weighted hyper-network is constructed, and the topological features of the network are extracted for classification. Main results. The experimental results obtained an optimal accuracy compared to the traditional coupling methods. The statistical results on network metrics proved that there were significant differences between depressive patients and normal controls. In addition, some brain regions and electrodes were found and discussed to highly correlate with depression by analyzing of the critical nodes and hyper-edges. Significance. These may help discover disease-related biomarkers important for depression diagnosis.

Studies have shown that attention bias can affect behavioral indicators in patients with depression, but it is still unclear how this bias affects the brain network topology of patients with mild depression (MD). Therefore, a novel functional brain network analysis and hierarchical clustering methods were used to explore the abnormal brain topology of MD patients based on EEG signals during the visual search paradigm. The behavior results showed that the reaction time of MD group was significantly higher than that of normal group. The results of functional brain network indicated significant differences in functional connections between the two groups, the amount of inter-hemispheric long-distance connections are much larger than intra-hemispheric short-distance connections. Patients with MD showed significantly lower local efficiency and clustering coefficient, destroyed community structure of frontal lobe and parietal-occipital lobe, frontal asymmetry, especially in beta band. In addition, the average value of long-distance connections between left frontal and right parietal-occipital lobes presented significant correlation with depressive symptoms. Our results suggested that MD patients achieved long-distance connections between the frontal and parietal-occipital regions by sacrificing the connections within the regions, which might provide new insights into the abnormal cognitive processing mechanism of depression.

Objective. Depression is accompanied by abnormalities in large-scale functional brain networks. This paper combined static and dynamic methods to analyze the abnormal topology and changes of functional connectivity network (FCN) of depression. Methods. We collected resting-state EEG recordings from 27 depressed subjects and 28 normal subjects, then obtained 68 regions of interests (ROIs) by source localization. We took ROIs as the nodes and correlations as the edges to build FCNs and analyzed static network based on graph theory. We used a sliding window method followed by k-means clustering, states analyses and trend analysis of network metrics over time to study dynamic connectivity. Results. The clustering coefficient (CC) and local efficiency in depression were increased, the characteristic path length and global efficiency were decreased, and local metrics had different manifestations in different resting state networks (RSNs); Depression had reduced connectivity in most RSNs, but increased connectivity in the default mode network, and there was a decoupling phenomenon between different RSNs; Depressed patients spent more time in sparsely connected states, their FCN's flexibility was less than normal subjects; The trend of CC over time was opposite between two groups. Most metrics in normal showed a relatively stronger correlation with time. Significance. Our research may provide a deeper understanding of neurophysiological mechanisms of depression and new biomarkers for clinical diagnosis of depression.