The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint
Author(s)
Type
Journal Article
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.
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.
Date Issued
2019-04-01
Date Acceptance
2019-01-31
Citation
NeuroImage, 2019, 189, pp.645-654
ISSN
1053-8119
Publisher
Elsevier
Start Page
645
End Page
654
Journal / Book Title
NeuroImage
Volume
189
Copyright Statement
© 2019 Published by Elsevier Inc.
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000461166900055&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
Science & Technology
Life Sciences & Biomedicine
Neurosciences
Neuroimaging
Radiology, Nuclear Medicine & Medical Imaging
Neurosciences & Neurology
Frontotemporal dementia
Mutation
Granulin
Microtuble associate protein tau
C9orf72
resting-state fMRI
Dynamic brain functional connectivity
Chronnectome
DYNAMIC FUNCTIONAL CONNECTIVITY
RESTING-STATE NETWORKS
FMRI DATA
BEHAVIORAL VARIANT
LOBAR DEGENERATION
FREQUENCY
SENSITIVITY
PATTERNS
SUBJECT
MOTION
Publication Status
Published
Date Publish Online
2019-02-01