Utilize este identificador para referenciar este registo: http://hdl.handle.net/10451/52438
Título: White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort
Autor: Sudre, Carole H.
Bocchetta, Martina
Cash, David
Thomas, David L.
Woollacott, Ione
Dick, Katrina M.
van Swieten, John
Borroni, Barbara
Galimberti, Daniela
Masellis, Mario
Tartaglia, Maria Carmela
Rowe, James B.
Graff, Caroline
Tagliavini, Fabrizio
Frisoni, Giovanni
Laforce, Robert
Finger, Elizabeth
De Mendonça, Alexandre
Sorbi, Sandro
Ourselin, Sébastien
Cardoso, M. Jorge
Rohrer, Jonathan D.
Andersson, Christin
Archetti, Silvana
Arighi, Andrea
Benussi, Luisa
Binetti, Giuliano
Black, Sandra
Cosseddu, Maura
Fallström, Marie
Ferreira, Carlos
Fenoglio, Chiara
Fox, Nick C.
Freedman, Morris
Fumagalli, Giorgio
Gazzina, Stefano
Ghidoni, Roberta
Grisoli, Marina
Jelic, Vesna
Jiskoot, Lize
Keren, Ron
Lombardi, Gemma
Maruta, Carolina
Mead, Simon
Meeter, Lieke
van Minkelen, Rick
Nacmias, Benedetta
Öijerstedt, Linn
Padovani, Alessandro
Panman, Jessica
Pievani, Michela
Polito, Cristina
Premi, Enrico
Prioni, Sara
Rademakers, Rosa
Redaelli, Veronica
Rogaeva, Ekaterina
Rossi, Giacomina
Rossor, Martin N.
Scarpini, Elio
Tang-Wai, David
Thonberg, Hakan
Tiraboschi, Pietro
Verdelho, Ana
Warren, Jason D.
Palavras-chave: CI, Confidence interval
FTD, Frontotemporal dementia
IQR, Inter Quartile Range
PS, Presymptomatic
S, Symptomatic
TIV, Total Intracranial volume
WMH, White matter hyperintensity
Data: 2017
Editora: Elsevier
Citação: Neuroimage Clin. 2017 Apr 26;15:171-180
Resumo: Genetic frontotemporal dementia is most commonly caused by mutations in the progranulin (GRN), microtubule-associated protein tau (MAPT) and chromosome 9 open reading frame 72 (C9orf72) genes. Previous small studies have reported the presence of cerebral white matter hyperintensities (WMH) in genetic FTD but this has not been systematically studied across the different mutations. In this study WMH were assessed in 180 participants from the Genetic FTD Initiative (GENFI) with 3D T1- and T2-weighed magnetic resonance images: 43 symptomatic (7 GRN, 13 MAPT and 23 C9orf72), 61 presymptomatic mutation carriers (25 GRN, 8 MAPT and 28 C9orf72) and 76 mutation negative non-carrier family members. An automatic detection and quantification algorithm was developed for determining load, location and appearance of WMH. Significant differences were seen only in the symptomatic GRN group compared with the other groups with no differences in the MAPT or C9orf72 groups: increased global load of WMH was seen, with WMH located in the frontal and occipital lobes more so than the parietal lobes, and nearer to the ventricles rather than juxtacortical. Although no differences were seen in the presymptomatic group as a whole, in the GRN cohort only there was an association of increased WMH volume with expected years from symptom onset. The appearance of the WMH was also different in the GRN group compared with the other groups, with the lesions in the GRN group being more similar to each other. The presence of WMH in those with progranulin deficiency may be related to the known role of progranulin in neuroinflammation, although other roles are also proposed including an effect on blood-brain barrier permeability and the cerebral vasculature. Future studies will be useful to investigate the longitudinal evolution of WMH and their potential use as a biomarker as well as post-mortem studies investigating the histopathological nature of the lesions.
Descrição: © 2017 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/BY/4.0/).
Peer review: yes
URI: http://hdl.handle.net/10451/52438
DOI: 10.1016/j.nicl.2017.04.015
Versão do Editor: https://www.sciencedirect.com/journal/neuroimage-clinical
Aparece nas colecções:FM - Artigos em Revistas Internacionais

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