Literature DB >> 30716457

The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint.

Enrico Premi1, Vince D Calhoun2, Matteo Diano3, Stefano Gazzina4, Maura Cosseddu4, Antonella Alberici4, Silvana Archetti5, Donata Paternicò4, Roberto Gasparotti6, John van Swieten7, Daniela Galimberti8, Raquel Sanchez-Valle9, Robert Laforce10, Fermin Moreno11, Matthis Synofzik12, Caroline Graff13, Mario Masellis14, Maria Carmela Tartaglia15, James Rowe16, Rik Vandenberghe17, Elizabeth Finger18, Fabrizio Tagliavini19, Alexandre de Mendonça20, Isabel Santana21, Chris Butler22, Simon Ducharme23, Alex Gerhard24, Adrian Danek25, Johannes Levin25, Markus Otto26, Giovanni Frisoni27, Stefano Cappa28, Sandro Sorbi29, Alessandro Padovani4, Jonathan D Rohrer30, Barbara Borroni31.   

Abstract

Frontotemporal Dementia (FTD) is preceded by a long period of subtle brain changes, occurring in the absence of overt cognitive symptoms, that need to be still fully characterized. Dynamic network analysis based on resting-state magnetic resonance imaging (rs-fMRI) is a potentially powerful tool for the study of preclinical FTD. In the present study, we employed a "chronnectome" approach (recurring, time-varying patterns of connectivity) to evaluate measures of dynamic connectivity in 472 at-risk FTD subjects from the Genetic Frontotemporal dementia research Initiative (GENFI) cohort. We considered 249 subjects with FTD-related pathogenetic mutations and 223 mutation non-carriers (HC). Dynamic connectivity was evaluated using independent component analysis and sliding-time window correlation to rs-fMRI data, and meta-state measures of global brain flexibility were extracted. Results show that presymptomatic FTD exhibits diminished dynamic fluidity, visiting less meta-states, shifting less often across them, and travelling through a narrowed meta-state distance, as compared to HC. Dynamic connectivity changes characterize preclinical FTD, arguing for the desynchronization of the inner fluctuations of the brain. These changes antedate clinical symptoms, and might represent an early signature of FTD to be used as a biomarker in clinical trials. Crown
Copyright © 2019. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  C9orf72; Chronnectome; Dynamic brain functional connectivity; Frontotemporal dementia; Granulin; Microtuble associate protein tau; Mutation; resting-state fMRI

Mesh:

Year:  2019        PMID: 30716457      PMCID: PMC6669888          DOI: 10.1016/j.neuroimage.2019.01.080

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


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