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Functional cognitive disorder: dementia's blind spot.
Ball, Harriet A; McWhirter, Laura; Ballard, Clive; Bhome, Rohan; Blackburn, Daniel J; Edwards, Mark J; Fleming, Stephen M; Fox, Nick C; Howard, Robert; Huntley, Jonathan; Isaacs, Jeremy D; Larner, Andrew J; Nicholson, Timothy R; Pennington, Catherine M; Poole, Norman; Price, Gary; Price, Jason P; Reuber, Markus; Ritchie, Craig; Rossor, Martin N; Schott, Jonathan M; Teodoro, Tiago; Venneri, Annalena; Stone, Jon; Carson, Alan J.
Afiliação
  • Ball HA; Population Health Sciences, University of Bristol, BS8 1QU, UK.
  • McWhirter L; Centre for Clinical Brain Sciences, The University of Edinburgh, EH16 4SB, UK.
  • Ballard C; College of Medicine and Health, University of Exeter, EX1 2LU, UK.
  • Bhome R; Division of Psychiatry, University College London, W1T 7NF, UK.
  • Blackburn DJ; Department of Neuroscience, Medical School, The University of Sheffield, S10 2TN, UK.
  • Edwards MJ; Neuroscience Research Centre, St George's, University of London, SW17 0RE, UK.
  • Fleming SM; Wellcome Centre for Human Neuroimaging, University College London, WC1N 3AR, UK.
  • Fox NC; Dementia Research Centre, Department of Neurodegenerative Diseases, UCL Queen Square Institute of Neurology, WC1E 6BT, UK.
  • Howard R; Division of Psychiatry, University College London, W1T 7NF, UK.
  • Huntley J; Division of Psychiatry, University College London, W1T 7NF, UK.
  • Isaacs JD; Neuroscience Research Centre, St George's, University of London, SW17 0RE, UK.
  • Larner AJ; Department of Neurology, St George's University Hospitals NHS Foundation Trust, London, SW17 0QT, UK.
  • Nicholson TR; Cognitive Function Clinic, Walton Centre for Neurology and Neurosurgery, Liverpool, L9 7LJ, UK.
  • Pennington CM; Institute of Psychiatry Psychology and Neuroscience, King's College London, SE5 8AF, UK.
  • Poole N; Centre for Clinical Brain Sciences, The University of Edinburgh, EH16 4SB, UK.
  • Price G; Department of Neurology, St George's University Hospitals NHS Foundation Trust, London, SW17 0QT, UK.
  • Price JP; University College London Hospitals NHS Foundation Trust, NW1 2BU, UK.
  • Reuber M; Department of Neuropsychology, South Tees Hospitals NHS Foundation Trust, TS4 3BW, UK.
  • Ritchie C; Department of Neuroscience, Medical School, The University of Sheffield, S10 2TN, UK.
  • Rossor MN; Centre for Clinical Brain Sciences, The University of Edinburgh, EH16 4SB, UK.
  • Schott JM; Dementia Research Centre, Department of Neurodegenerative Diseases, UCL Queen Square Institute of Neurology, WC1E 6BT, UK.
  • Teodoro T; Dementia Research Centre, Department of Neurodegenerative Diseases, UCL Queen Square Institute of Neurology, WC1E 6BT, UK.
  • Venneri A; Neuroscience Research Centre, St George's, University of London, SW17 0RE, UK.
  • Stone J; Instituto de Medicina Molecular, Universidade de Lisbon, 1649-028 Lisboa, Portugal.
  • Carson AJ; Department of Neuroscience, Medical School, The University of Sheffield, S10 2TN, UK.
Brain ; 143(10): 2895-2903, 2020 10 01.
Article em En | MEDLINE | ID: mdl-32791521
ABSTRACT
An increasing proportion of cognitive difficulties are recognized to have a functional cause, the chief clinical indicator of which is internal inconsistency. When these symptoms are impairing or distressing, and not better explained by other disorders, this can be conceptualized as a cognitive variant of functional neurological disorder, termed functional cognitive disorder (FCD). FCD is likely very common in clinical practice but may be under-diagnosed. Clinicians in many settings make liberal use of the descriptive term mild cognitive impairment (MCI) for those with cognitive difficulties not impairing enough to qualify as dementia. However, MCI is an aetiology-neutral description, which therefore includes patients with a wide range of underlying causes. Consequently, a proportion of MCI cases are due to non-neurodegenerative processes, including FCD. Indeed, significant numbers of patients diagnosed with MCI do not 'convert' to dementia. The lack of diagnostic specificity for MCI 'non-progressors' is a weakness inherent in framing MCI primarily within a deterministic neurodegenerative pathway. It is recognized that depression, anxiety and behavioural changes can represent a prodrome to neurodegeneration; empirical data are required to explore whether the same might hold for subsets of individuals with FCD. Clinicians and researchers can improve study efficacy and patient outcomes by viewing MCI as a descriptive term with a wide differential diagnosis, including potentially reversible components such as FCD. We present a preliminary definition of functional neurological disorder-cognitive subtype, explain its position in relation to other cognitive diagnoses and emerging biomarkers, highlight clinical features that can lead to positive diagnosis (as opposed to a diagnosis of exclusion), and red flags that should prompt consideration of alternative diagnoses. In the research setting, positive identifiers of FCD will enhance our recognition of individuals who are not in a neurodegenerative prodrome, while greater use of this diagnosis in clinical practice will facilitate personalized interventions.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progressão da Doença / Demência / Disfunção Cognitiva Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progressão da Doença / Demência / Disfunção Cognitiva Idioma: En Ano de publicação: 2020 Tipo de documento: Article