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Neuropsychiatric symptoms in genetic frontotemporal dementia: developing a new module for Clinical Rating Scales.
Samra, Kiran; Macdougall, Amy; Peakman, Georgia; Bouzigues, Arabella; Bocchetta, Martina; Cash, David M; Greaves, Caroline V; Convery, Rhian S; van Swieten, John C; Jiskoot, Lize C; Seelaar, Harro; Moreno, Fermin; Sánchez-Valle, Raquel; Laforce, Robert; Graff, Caroline; Masellis, Mario; Tartaglia, Maria Carmela; Rowe, James B; Borroni, Barbara; Finger, Elizabeth; Synofzik, Matthis; Galimberti, Daniela; Vandenberghe, Rik; de Mendonca, Alexandre; Butler, Christopher R; Gerhard, Alexander; Ducharme, Simon; Le Ber, Isabelle; Tiraboschi, Pietro; Santana, Isabel; Pasquier, Florence; Levin, Johannes; Otto, Markus; Sorbi, Sandro; Rohrer, Jonathan D; Russell, Lucy L.
Afiliação
  • Samra K; Dementia Reseach Centre, Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK.
  • Macdougall A; London School of Hygiene & Tropical Medicine, London, UK.
  • Peakman G; Dementia Reseach Centre, Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK.
  • Bouzigues A; Dementia Reseach Centre, Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK.
  • Bocchetta M; Dementia Reseach Centre, Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK.
  • Cash DM; Dementia Reseach Centre, Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK.
  • Greaves CV; Centre for Medical Image Computing, University College London, London, UK.
  • Convery RS; Dementia Reseach Centre, Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK.
  • van Swieten JC; Dementia Reseach Centre, Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK.
  • Jiskoot LC; Neurology, Erasmus MC, Rotterdam, The Netherlands.
  • Seelaar H; Neurology, Erasmus MC, Rotterdam, The Netherlands.
  • Moreno F; Neurology, Erasmus MC Alzheimer Centre, Rotterdam, The Netherlands.
  • Sánchez-Valle R; Cognitive Disorders Unit, Department of Neurology, Donostia University Hospital Gipuzkoa Building, San Sebastian, Spain.
  • Laforce R; Alzheimer's Disease and Other Cognitive Disorders Unit, Neurology Service, Hospital Clinic de Barcelona, Barcelona, Spain.
  • Graff C; Interdisciplinary Memory Clinic, Department of Neurological Sciences, Laval University, Quebec, Quebec, Canada.
  • Masellis M; Center for Alzheimer Research, Division of Neurogeriatrics, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
  • Tartaglia MC; Unit for Hereditary Dementias, Theme Aging, Karolinska University Hospital, Solna, Sweden.
  • Rowe JB; Neurology, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
  • Borroni B; Tanz Centre for Research in Neurodegenerative Disease, University of Toronto, Toronto, Ontario, Canada.
  • Finger E; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Synofzik M; Centre for Ageing Brain and Neurodegenerative Disorders, Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
  • Galimberti D; Clinical Neurological Sciences, University of Western Ontario, London, Ontario, Canada.
  • Vandenberghe R; Dept. of Neurodegenerative Diseases, Eberhard Karls University Tubingen Hertie Institute for Clinical Brain Research, Tubingen, Germany.
  • de Mendonca A; Department of Neurological Sciences, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Butler CR; Laboratory for Cognitive Neurology, Department of Neurosciences, KU Leuven, Leuven, Belgium.
  • Gerhard A; Neurology Service, KU Leuven University Hospitals Leuven, Leuven, Belgium.
  • Ducharme S; Faculty of Medicine, University of Lisbon, Lisboa, Portugal.
  • Le Ber I; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
  • Tiraboschi P; Department of Brain Sciences, Imperial College London, London, UK.
  • Santana I; Division of Neuroscience and Experimental Psychology, The University of Manchester, Manchester, UK.
  • Pasquier F; Departments of Geriatric Medicine and Nuclear Medicine, University of Duisburg-Essen, Duisburg, Germany.
  • Levin J; McConnell Brain Imaging Centre, Department of Neurology & Neurosurgery, Montreal Neurological Institute and Hospital, Montreal, Québec, Canada.
  • Otto M; Douglas Mental Health University Institute, Department of Psychiatry, McGill University, Montreal, Québec, Canada.
  • Sorbi S; Inserm U1127, CNRS UMR 7225, FrontLab - Reference Centre for Rare or Early Dementias, IM2A, Département de Neurologie, Hôpital Universitaire Pitié Salpêtrière, Sorbonne Université, Paris Brain Institute - Institut du Cerveau - ICM, Paris, France.
  • Rohrer JD; National Reference Center On Rare Dementias, Groupe Hospitalier La Pitié Salpêtrière-Charles Foix, Paris, France.
  • Russell LL; Division of Neurology V and Neuropathology, Foundation IRCCS Carlo Besta Neurological Institute, Milano, Italy.
J Neurol Neurosurg Psychiatry ; 94(5): 357-368, 2023 05.
Article em En | MEDLINE | ID: mdl-36627201
ABSTRACT

BACKGROUND:

Current clinical rating scales in frontotemporal dementia (FTD) often do not incorporate neuropsychiatric features and may therefore inadequately measure disease stage.

METHODS:

832 participants from the Genetic FTD Initiative (GENFI) were recruited 522 mutation carriers and 310 mutation-negative controls. The standardised GENFI clinical questionnaire assessed the frequency and severity of 14 neuropsychiatric symptoms visual, auditory, and tactile hallucinations, delusions, depression, anxiety, irritability/lability, agitation/aggression, euphoria/elation, aberrant motor behaviour, hypersexuality, hyperreligiosity, impaired sleep, and altered sense of humour. A principal component analysis (PCA) was performed to identify key groupings of neuropsychiatric and behavioural items in order to create a new neuropsychiatric module that could be used as an addition to the Clinical Dementia Rating (CDR) plus National Alzheimer's Coordinating Center Behaviour and Language Domains (NACC FTLD) rating scale.

RESULTS:

Overall, 46.4% of mutation carriers had neuropsychiatric symptoms (51.6% C9orf72, 40.8% GRN, 46.6% MAPT) compared with 24.5% of controls. Anxiety and depression were the most common in all genetic groups but fluctuated longitudinally and loaded separately in the PCA. Hallucinations and delusions loaded together, with the remaining neuropsychiatric symptoms loading with the core behavioural features of FTD. These results suggest using a single 'psychosis' neuropsychiatric module consisting of hallucinations and delusions. Adding this to the CDR plus NACC FTLD, called the CDR plus NACC FTLD-N, leads to a number of participants being scored more severely, including those who were previously considered asymptomatic now being scored as prodromal.

CONCLUSIONS:

Neuropsychiatric symptoms occur in mutation carriers at all disease stages across all three genetic groups. However, only psychosis features provided additional staging benefit to the CDR plus NACC FTLD. Inclusion of these features brings us closer to optimising the rating scale for use in trials.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Demência Frontotemporal Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: J Neurol Neurosurg Psychiatry Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Demência Frontotemporal Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: J Neurol Neurosurg Psychiatry Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido