Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study.
Adult
Aged
Brain
/ metabolism
C9orf72 Protein
/ genetics
Cerebrovascular Circulation
/ genetics
Cross-Sectional Studies
Female
Frontotemporal Dementia
/ genetics
Heterozygote
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Mutation
Neuropsychological Tests
Progranulins
/ genetics
tau Proteins
/ genetics
arterial spin labelling
cerebral blood flow
genetic frontotemporal dementia
presymptomatic biomarker
Journal
Brain : a journal of neurology
ISSN: 1460-2156
Titre abrégé: Brain
Pays: England
ID NLM: 0372537
Informations de publication
Date de publication:
01 04 2019
01 04 2019
Historique:
received:
14
10
2018
revised:
14
12
2018
accepted:
04
01
2019
pubmed:
9
3
2019
medline:
18
12
2019
entrez:
9
3
2019
Statut:
ppublish
Résumé
Genetic forms of frontotemporal dementia are most commonly due to mutations in three genes, C9orf72, GRN or MAPT, with presymptomatic carriers from families representing those at risk. While cerebral blood flow shows differences between frontotemporal dementia and other forms of dementia, there is limited evidence of its utility in presymptomatic stages of frontotemporal dementia. This study aimed to delineate the cerebral blood flow signature of presymptomatic, genetic frontotemporal dementia using a voxel-based approach. In the multicentre GENetic Frontotemporal dementia Initiative (GENFI) study, we investigated cross-sectional differences in arterial spin labelling MRI-based cerebral blood flow between presymptomatic C9orf72, GRN or MAPT mutation carriers (n = 107) and non-carriers (n = 113), using general linear mixed-effects models and voxel-based analyses. Cerebral blood flow within regions of interest derived from this model was then explored to identify differences between individual gene carrier groups and to estimate a timeframe for the expression of these differences. The voxel-based analysis revealed a significant inverse association between cerebral blood flow and the expected age of symptom onset in carriers, but not non-carriers. Regions included the bilateral insulae/orbitofrontal cortices, anterior cingulate/paracingulate gyri, and inferior parietal cortices, as well as the left middle temporal gyrus. For all bilateral regions, associations were greater on the right side. After correction for partial volume effects in a region of interest analysis, the results were found to be largely driven by the C9orf72 genetic subgroup. These cerebral blood flow differences first appeared approximately 12.5 years before the expected symptom onset determined on an individual basis. Cerebral blood flow was lower in presymptomatic mutation carriers closer to and beyond their expected age of symptom onset in key frontotemporal dementia signature regions. These results suggest that arterial spin labelling MRI may be a promising non-invasive imaging biomarker for the presymptomatic stages of genetic frontotemporal dementia.
Identifiants
pubmed: 30847466
pii: 5371511
doi: 10.1093/brain/awz039
pmc: PMC6439322
doi:
Substances chimiques
C9orf72 Protein
0
C9orf72 protein, human
0
GRN protein, human
0
MAPT protein, human
0
Progranulins
0
tau Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1108-1120Subventions
Organisme : Medical Research Council
ID : MC_U123160651
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00024/1
Pays : United Kingdom
Organisme : CIHR
ID : MOP 327387
Pays : Canada
Organisme : Medical Research Council
ID : MR/J009482/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M023664/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M008525/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M009041/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M024873/1
Pays : United Kingdom
Investigateurs
Christin Andersson
(C)
Silvia Archetti
(S)
Andrea Arighi
(A)
Luisa Benussi
(L)
Giuliano Binetti
(G)
Maura Cosseddu
(M)
Katrina M Dick
(KM)
Marie Fallström
(M)
Carlos Ferreira
(C)
Chiara Fenoglio
(C)
Nick C Fox
(NC)
Giorgio Fumagalli
(G)
Stefano Gazzina
(S)
Roberta Ghidoni
(R)
Marina Grisoli
(M)
Vesna Jelic
(V)
Lize Jiskoot
(L)
Gemma Lombardi
(G)
Carolina Maruta
(C)
Simon Mead
(S)
Lieke Meeter
(L)
Rick van Minkelen
(R)
Benedetta Nacmias
(B)
Linn Öijerstedt
(L)
Sebastien Ourselin
(S)
Alessandro Padovani
(A)
Jessica Panman
(J)
Michela Pievani
(M)
Cristina Polito
(C)
Enrico Premi
(E)
Sara Prioni
(S)
Rosa Rademakers
(R)
Veronica Redaelli
(V)
Giacomina Rossi
(G)
Martin N Rossor
(MN)
Elio Scarpini
(E)
Hakan Thonberg
(H)
Pietro Tiraboschi
(P)
Ana Verdelho
(A)
Jason D Warren
(JD)
Commentaires et corrections
Type : ErratumIn
Informations de copyright
© The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain.
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