arXiv subjects

Jeremy Guillon

Publications and source records attributed to Jeremy Guillon.

3 recordsLinked to original sources

arXiv2018

Disrupted core-periphery structure of multimodal brain networks in Alzheimer's Disease

In Alzheimer's disease (AD), the progressive atrophy leads to aberrant network reconfigurations both at structural and functional levels. In such network reorganization, the core and peripheral nodes appear to be crucial for the prediction of clinical outcome due to their ability to influence large-scale functional integration. However, the role of the different types of brain connectivity in such prediction still remains unclear. Using a multiplex network approach we integrated information from DWI, fMRI and MEG brain connectivity to extract an enriched description of the core-periphery structure in a group of AD patients and age-matched controls. Globally, the regional coreness - i.e., the probability of a region to be in the multiplex core - significantly decreased in AD patients as a result of the randomization process initiated by the neurodegeneration. Locally, the most impacted areas were in the core of the network - including temporal, parietal and occipital areas - while we reported compensatory increments for the peripheral regions in the sensorimotor system. Furthermore, these network changes significantly predicted the cognitive and memory impairment of patients. Taken together these results indicate that a more accurate description of neurodegenerative diseases can be obtained from the multimodal integration of neuroimaging-derived network data.

q-bio.NC↗

arXiv2017

Multiplex core-periphery organization of the human connectome

The behavior of many complex systems is determined by a core of densely interconnected units. While many methods are available to identify the core of a network when connections between nodes are all of the same type, a principled approach to define the core when multiple types of connectivity are allowed is still lacking. Here we introduce a general framework to define and extract the core-periphery structure of multi-layer networks by explicitly taking into account the connectivity of the nodes at each layer. We show how our method works on synthetic networks with different size, density, and overlap between the cores at the different layers. We then apply the method to multiplex brain networks whose layers encode information both on the anatomical and the functional connectivity among regions of the human cortex. Results confirm the presence of the main known hubs, but also suggest the existence of novel brain core regions that have been discarded by previous analysis which focused exclusively on the structural layer. Our work is a step forward in the identification of the core of the human connectome, and contributes to shed light to a fundamental question in modern neuroscience.

q-bio.NC↗

arXiv2017

Loss of brain inter-frequency hubs in Alzheimer's disease

Alzheimer's disease (AD) causes alterations of brain network structure and function. The latter consists of connectivity changes between oscillatory processes at different frequency channels. We proposed a multi-layer network approach to analyze multiple-frequency brain networks inferred from magnetoencephalographic recordings during resting-states in AD subjects and age-matched controls. Main results showed that brain networks tend to facilitate information propagation across different frequencies, as measured by the multi-participation coefficient (MPC). However, regional connectivity in AD subjects was abnormally distributed across frequency bands as compared to controls, causing significant decreases of MPC. This effect was mainly localized in association areas and in the cingulate cortex, which acted, in the healthy group, as a true inter-frequency hub. MPC values significantly correlated with memory impairment of AD subjects, as measured by the total recall score. Most predictive regions belonged to components of the default-mode network that are typically affected by atrophy, metabolism disruption and amyloid-beta deposition. We evaluated the diagnostic power of the MPC and we showed that it led to increased classification accuracy (78.39%) and sensitivity (91.11%). These findings shed new light on the brain functional alterations underlying AD and provide analytical tools for identifying multi-frequency neural mechanisms of brain diseases.

q-bio.NC↗