Disrupted core-periphery structure of multimodal brain networks in Alzheimer’s disease

Jeremy Guillon, Mario Chavez, Federico Battiston, Yohan Attal, Valentina La Corte, Michel Thiebaut de Schotten, Bruno Dubois, Denis Schwartz, Olivier Colliot, Fabrizio De Vico Fallani

Research output: Contribution to journalArticlepeer-review

Abstract (may include machine translation)

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 because of 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—that is, the probability of a region to be in the multiplex core—significantly decreased in AD patients as result of a random disconnection 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.

Original languageEnglish
Pages (from-to)635-652
Number of pages18
JournalNetwork Neuroscience
Volume3
Issue number2
DOIs
StatePublished - 1 Jan 2019

Keywords

  • Brain connectivity
  • DWI
  • FMRI
  • MEG
  • Multilayer network theory
  • Neurodegenerative diseases

Fingerprint

Dive into the research topics of 'Disrupted core-periphery structure of multimodal brain networks in Alzheimer’s disease'. Together they form a unique fingerprint.

Cite this