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@ARTICLE{Premi:140568,
author = {Premi, Enrico and Calhoun, Vince D and Diano, Matteo and
Gazzina, Stefano and Cosseddu, Maura and Alberici, Antonella
and Archetti, Silvana and Paternicò, Donata and Gasparotti,
Roberto and van Swieten, John and Galimberti, Daniela and
Sanchez-Valle, Raquel and Laforce, Robert and Moreno, Fermin
and Synofzik, Matthis and Graff, Caroline and Masellis,
Mario and Tartaglia, Maria Carmela and Rowe, James and
Vandenberghe, Rik and Finger, Elizabeth and Tagliavini,
Fabrizio and de Mendonça, Alexandre and Santana, Isabel and
Butler, Chris and Ducharme, Simon and Gerhard, Alex and
Danek, Adrian and Levin, Johannes and Otto, Markus and
Frisoni, Giovanni and Cappa, Stefano and Sorbi, Sandro and
Padovani, Alessandro and Rohrer, Jonathan D and Borroni,
Barbara and Genetic FTD Initiative, GENFI and Almeida, Maria
Rosario and Anderl-Straub, Sarah and Andersson, Christin and
Antonell, Anna and Arighi, Andrea and Balasa, Mircea and
Barandiaran, Myriam and Bargalló, Nuria and Bartha, Robart
and Bender, Benjamin and Benussi, Luisa and Binetti,
Giuliano and Black, Sandra and Bocchetta, Martina and
Borrego-Ecija, Sergi and Bras, Jose and Bruffaerts, Rose and
Caroppo, Paola and Cash, David and Castelo-Branco, Miguel
and Convery, Rhian and Cope, Thomas and de Arriba, María
and Di Fede, Giuseppe and Díaz, Zigor and Dick, Katrina M
and Duro, Diana and Fenoglio, Chiara and Ferreira, Carlos
and Ferreira, Catarina B and Flanagan, Toby and Fox, Nick
and Freedman, Morris and Fumagalli, Giorgio and Gabilondo,
Alazne and Gauthier, Serge and Ghidoni, Roberta and
Giaccone, Giorgio and Gorostidi, Ana and Greaves, Caroline
and Guerreiro, Rita and Heller, Carolin and Hoegen, Tobias
and Indakoetxea, Begoña and Jelic, Vesna and Jiskoot, Lize
and Karnath, Hans-Otto and Keren, Ron and Leitão, Maria
João and Lladó, Albert and Lombardi, Gemma and Loosli,
Sandra and Maruta, Carolina and Mead, Simon and Meeter,
Lieke and Miltenberger, Gabriel and van Minkelen, Rick and
Mitchell, Sara and Nacmias, Benedetta and Neason, Mollie and
Nicholas, Jennifer and Öijerstedt, Linn and Olives, Jaume
and Panman, Jessica and Papma, Janne and Patzig, Maximilian
and Pievani, Michela and Prioni, Sara and Prix, Catharina
and Rademakers, Rosa and Redaelli, Veronica and Rittman, Tim
and Rogaeva, Ekaterina and Rosa-Neto, Pedro and Rossi,
Giacomina and Rossor, Martin and Santiago, Beatriz and
Scarpini, Elio and Semler, Elisa and Shafei, Rachelle and
Shoesmith, Christen and Tábuas-Pereira, Miguel and Tainta,
Mikel and Tang-Wai, David and Thomas, David L and Thonberg,
Hakan and Timberlake, Carolyn and Tiraboschi, Pietro and
Vandamme, Philip and Vandenbulcke, Mathieu and Veldsman,
Michele and Verdelho, Ana and Villanua, Jorge and Warren,
Jason and Wilke, Carlo and Zetterberg, Henrik and Zulaica,
Miren},
title = {{T}he inner fluctuations of the brain in presymptomatic
{F}rontotemporal {D}ementia: {T}he chronnectome
fingerprint.},
journal = {NeuroImage},
volume = {189},
issn = {1053-8119},
address = {Orlando, Fla.},
publisher = {Academic Press},
reportid = {DZNE-2020-06890},
pages = {645-654},
year = {2019},
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.},
keywords = {Adult / Connectome: methods / Female / Frontotemporal
Dementia: diagnostic imaging / Frontotemporal Dementia:
genetics / Frontotemporal Dementia: physiopathology /
Heterozygote / Humans / Magnetic Resonance Imaging / Male /
Middle Aged / Nerve Net: diagnostic imaging / Nerve Net:
physiopathology / Prodromal Symptoms / Time Factors},
cin = {U Clinical Researchers - München / AG Levin},
ddc = {610},
cid = {I:(DE-2719)7000003 / I:(DE-2719)1111016},
pnm = {344 - Clinical and Health Care Research (POF3-344)},
pid = {G:(DE-HGF)POF3-344},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30716457},
pmc = {pmc:PMC6669888},
doi = {10.1016/j.neuroimage.2019.01.080},
url = {https://pub.dzne.de/record/140568},
}