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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 |
Ficheiros deste registo:
Ficheiro | Descrição | Tamanho | Formato | |
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White_matter.pdf | 3,05 MB | Adobe PDF | Ver/Abrir |
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