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Altered plasma protein profiles in genetic FTD - a GENFI study.
Ullgren, Abbe; Öijerstedt, Linn; Olofsson, Jennie; Bergström, Sofia; Remnestål, Julia; van Swieten, John C; Jiskoot, Lize C; Seelaar, Harro; Borroni, Barbara; Sanchez-Valle, Raquel; Moreno, Fermin; Laforce, Robert; Synofzik, Matthis; Galimberti, Daniela; Rowe, James B; Masellis, Mario; Tartaglia, Maria Carmela; Finger, Elizabeth; Vandenberghe, Rik; de Mendonça, Alexandre; Tirabosch, Pietro; Santana, Isabel; Ducharme, Simon; Butler, Chris R; Gerhard, Alexander; Otto, Markus; Bouzigues, Arabella; Russell, Lucy; Swift, Imogen J; Sogorb-Esteve, Aitana; Heller, Carolin; Rohrer, Jonathan D; Månberg, Anna; Nilsson, Peter; Graff, Caroline.
Afiliación
  • Ullgren A; Swedish FTD Initiative, Stockholm, Sweden.
  • Öijerstedt L; Department of Neurobiology, Care Sciences and Society, Division of Neurogeriatrics, Karolinska Institutet, Solna, Sweden.
  • Olofsson J; Unit for Hereditary Dementias, Karolinska University Hospital, Solna, Sweden.
  • Bergström S; Swedish FTD Initiative, Stockholm, Sweden.
  • Remnestål J; Department of Neurobiology, Care Sciences and Society, Division of Neurogeriatrics, Karolinska Institutet, Solna, Sweden.
  • van Swieten JC; Unit for Hereditary Dementias, Karolinska University Hospital, Solna, Sweden.
  • Jiskoot LC; Swedish FTD Initiative, Stockholm, Sweden.
  • Seelaar H; Department of Protein Science, Division of Affinity Proteomics, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.
  • Borroni B; Swedish FTD Initiative, Stockholm, Sweden.
  • Sanchez-Valle R; Department of Protein Science, Division of Affinity Proteomics, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.
  • Moreno F; Swedish FTD Initiative, Stockholm, Sweden.
  • Laforce R; Department of Protein Science, Division of Affinity Proteomics, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.
  • Synofzik M; Department of Neurology, Erasmus Medical Centre, Rotterdam, Netherlands.
  • Galimberti D; Department of Neurology, Erasmus Medical Centre, Rotterdam, Netherlands.
  • Rowe JB; Department of Neurology, Erasmus Medical Centre, Rotterdam, Netherlands.
  • Masellis M; Department of Clinical and Experimental Sciences, Centre for Neurodegenerative Disorders, University of Brescia, Brescia, Italy.
  • Tartaglia MC; Alzheimer's Disease and Other Cognitive Disorders Unit, Neurology Service, Hospital Clínic, Institut d'Investigacións Biomèdiques August Pi I Sunyer, University of Barcelona, Barcelona, Spain.
  • Finger E; Department of Neurology, Cognitive Disorders Unit, Donostia University Hospital, San Sebastian, Gipuzkoa, Spain.
  • Vandenberghe R; Neuroscience Area, Biodonostia Health Research Institute, San Sebastian, Gipuzkoa, Spain.
  • de Mendonça A; Département Des Sciences Neurologiques, Clinique Interdisciplinaire de Mémoire, CHU de Québec, and Faculté de Médecine, Université Laval, Quebec City, QC, Canada.
  • Tirabosch P; Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Tübingen, Germany.
  • Santana I; Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Ducharme S; Fondazione IRCCS Ospedale Policlinico, Milan, Italy.
  • Butler CR; University of Milan, Centro Dino Ferrari, Milan, Italy.
  • Gerhard A; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Otto M; Sunnybrook Health Sciences Centre, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
  • Bouzigues A; Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Canada.
  • Russell L; Department of Clinical Neurological Sciences, University of Western Ontario, London, ON, Canada.
  • Swift IJ; Department of Neurosciences, Laboratory for Cognitive Neurology, KU Leuven, Leuven, Belgium.
  • Sogorb-Esteve A; Neurology Service, University Hospitals Leuven, Leuven, Belgium.
  • Heller C; Leuven Brain Institute, KU Leuven, Leuven, Belgium.
  • Rohrer JD; Faculty of Medicine, University of Lisbon, Lisbon, Portugal.
  • Månberg A; Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
  • Nilsson P; Faculty of Medicine, University Hospital of Coimbra (HUC), Neurology Service, University of Coimbra, Coimbra, Portugal.
  • Graff C; Center for Neuroscience and Cell Biology, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Mol Neurodegener ; 18(1): 85, 2023 Nov 15.
Article en En | MEDLINE | ID: mdl-37968725
BACKGROUND: Plasma biomarkers reflecting the pathology of frontotemporal dementia would add significant value to clinical practice, to the design and implementation of treatment trials as well as our understanding of disease mechanisms. The aim of this study was to explore the levels of multiple plasma proteins in individuals from families with genetic frontotemporal dementia. METHODS: Blood samples from 693 participants in the GENetic Frontotemporal Dementia Initiative study were analysed using a multiplexed antibody array targeting 158 proteins. RESULTS: We found 13 elevated proteins in symptomatic mutation carriers, when comparing plasma levels from people diagnosed with genetic FTD to healthy non-mutation controls and 10 proteins that were elevated compared to presymptomatic mutation carriers. CONCLUSION: We identified plasma proteins with altered levels in symptomatic mutation carriers compared to non-carrier controls as well as to presymptomatic mutation carriers. Further investigations are needed to elucidate their potential as fluid biomarkers of the disease process.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Demencia Frontotemporal Límite: Humans Idioma: En Revista: Mol Neurodegener Año: 2023 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Demencia Frontotemporal Límite: Humans Idioma: En Revista: Mol Neurodegener Año: 2023 Tipo del documento: Article País de afiliación: Suecia