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Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study.
Mutsaerts, Henri J M M; Mirza, Saira S; Petr, Jan; Thomas, David L; Cash, David M; Bocchetta, Martina; de Vita, Enrico; Metcalfe, Arron W S; Shirzadi, Zahra; Robertson, Andrew D; Tartaglia, Maria Carmela; Mitchell, Sara B; Black, Sandra E; Freedman, Morris; Tang-Wai, David; Keren, Ron; Rogaeva, Ekaterina; van Swieten, John; Laforce, Robert; Tagliavini, Fabrizio; Borroni, Barbara; Galimberti, Daniela; Rowe, James B; Graff, Caroline; Frisoni, Giovanni B; Finger, Elizabeth; Sorbi, Sandro; de Mendonça, Alexandre; Rohrer, Jonathan D; MacIntosh, Bradley J; Masellis, Mario.
Afiliação
  • Mutsaerts HJMM; Hurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
  • Mirza SS; Hurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
  • Petr J; PET Center, Institute of Radiopharmaceutical Cancer Research, Helmholtz-Zentrum Dresden-Rossendorf, Dresden, Germany.
  • Thomas DL; Institute of Neurology, University College London, London, UK.
  • Cash DM; Institute of Neurology, University College London, London, UK.
  • Bocchetta M; Institute of Neurology, University College London, London, UK.
  • de Vita E; Institute of Neurology, University College London, London, UK.
  • Metcalfe AWS; Hurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
  • Shirzadi Z; Hurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
  • Robertson AD; Hurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
  • Tartaglia MC; Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Canada.
  • Mitchell SB; Memory Clinic, University Health Network, Toronto, Canada.
  • Black SE; Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada.
  • Freedman M; Hurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
  • Tang-Wai D; Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada.
  • Keren R; L.C. Campbell Cognitive Neurology Research Unit, Sunnybrook Health Sciences Centre, Toronto, Canada.
  • Rogaeva E; Hurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
  • van Swieten J; Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada.
  • Laforce R; L.C. Campbell Cognitive Neurology Research Unit, Sunnybrook Health Sciences Centre, Toronto, Canada.
  • Tagliavini F; Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada.
  • Borroni B; Baycrest Centre for Geriatric Care, Toronto, Canada.
  • Galimberti D; Memory Clinic, University Health Network, Toronto, Canada.
  • Rowe JB; Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada.
  • Graff C; Memory Clinic, University Health Network, Toronto, Canada.
  • Frisoni GB; Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Canada.
  • Finger E; Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Sorbi S; Clinique Interdisciplinaire de Mémoire (CIME), Département des Sciences Neurologiques, CHU de Québec, Faculté de médecine, Université Laval, Québec, Canada.
  • de Mendonça A; Fondazione Istituto di Ricovero e Cura a Carattere Scientifico, Milan, Italy.
  • Rohrer JD; Department of Medical and Experimental Sciences, University of Brescia, Brescia, Italy.
  • MacIntosh BJ; Centro Dino Ferrari, Fondazione Ca' Granda IRCCS Ospedale Policlinico, University of Milan, Milan, Italy.
  • Masellis M; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Brain ; 142(4): 1108-1120, 2019 04 01.
Article em En | MEDLINE | ID: mdl-30847466
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Circulação Cerebrovascular / Demência Frontotemporal Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Brain Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Circulação Cerebrovascular / Demência Frontotemporal Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Brain Ano de publicação: 2019 Tipo de documento: Article