Multiplex Networks for Early Diagnosis of Alzheimer's Disease

Analysis and quantification of brain structural changes, using Magnetic Resonance Imaging (MRI), are increasingly used to define novel biomarkers of brain pathologies, such as Alzheimer's disease (AD). Several studies have suggested that brain topological organization can reveal early signs of...

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Published inFrontiers in aging neuroscience Vol. 10; p. 365
Main Authors Amoroso, Nicola, La Rocca, Marianna, Bruno, Stefania, Maggipinto, Tommaso, Monaco, Alfonso, Bellotti, Roberto, Tangaro, Sabina
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Research Foundation 14.11.2018
Frontiers Media S.A
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ISSN1663-4365
1663-4365
DOI10.3389/fnagi.2018.00365

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Summary:Analysis and quantification of brain structural changes, using Magnetic Resonance Imaging (MRI), are increasingly used to define novel biomarkers of brain pathologies, such as Alzheimer's disease (AD). Several studies have suggested that brain topological organization can reveal early signs of AD. Here, we propose a novel brain model which captures both intra- and inter-subject information within a multiplex network approach. This model localizes brain atrophy effects and summarizes them with a diagnostic score. On an independent test set, our multiplex-based score segregates (i) normal controls (NC) from AD patients with a 0.86±0.01 accuracy and (ii) NC from mild cognitive impairment (MCI) subjects that will convert to AD (cMCI) with an accuracy of 0.84±0.01. The model shows that illness effects are maximally detected by parceling the brain in equal volumes of 3, 000 mm ("patches"), without any segmentation based on anatomical features. The multiplex approach shows great sensitivity in detecting anomalous changes in the brain; the robustness of the obtained results is assessed using both voxel-based morphometry and FreeSurfer morphological features. Because of its generality this method can provide a reliable tool for clinical trials and a disease signature of many neurodegenerative pathologies.
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Reviewed by: Patrizia Giannoni, University of Nîmes, France; Ghulam Md Ashraf, King Abdulaziz University, Saudi Arabia
Data used in preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. More details are given in the Acknowledgments
Edited by: Fernanda Laezza, The University of Texas Medical Branch at Galveston, United States
These authors have contributed equally to this work and last authorship
ISSN:1663-4365
1663-4365
DOI:10.3389/fnagi.2018.00365