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Plasma Neurofilament Light as a Biomarker of Neurological Involvement in Wilson's Disease.
Shribman, Samuel; Heller, Carolin; Burrows, Maggie; Heslegrave, Amanda; Swift, Imogen; Foiani, Martha S; Gillett, Godfrey T; Tsochatzis, Emmanuel A; Rowe, James B; Gerhard, Alex; Butler, Chris R; Masellis, Mario; Bremner, Fion; Martin, Alison; Jung, Lynne; Cook, Paul; Zetterberg, Henrik; Bandmann, Oliver; Rohrer, Jonathan D; Warner, Thomas T.
Affiliation
  • Shribman S; Department of Clinical and Movement Neurosciences, Reta Lila Weston Institute, UCL Queen Square Institute of Neurology, London, United Kingdom.
  • Heller C; Dementia Research Centre, Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, United Kingdom.
  • Burrows M; Department of Neurodegenerative Disease, UK Dementia Research Institute, UCL Queen Square Institute of Neurology, London, United Kingdom.
  • Heslegrave A; Department of Clinical and Movement Neurosciences, Reta Lila Weston Institute, UCL Queen Square Institute of Neurology, London, United Kingdom.
  • Swift I; Department of Neurodegenerative Disease, UK Dementia Research Institute, UCL Queen Square Institute of Neurology, London, United Kingdom.
  • Foiani MS; Department of Neurodegenerative Disease, UK Dementia Research Institute, UCL Queen Square Institute of Neurology, London, United Kingdom.
  • Gillett GT; Department of Neurodegenerative Disease, UK Dementia Research Institute, UCL Queen Square Institute of Neurology, London, United Kingdom.
  • Tsochatzis EA; Department of Clinical Chemistry, Northern General Hospital, Sheffield, United Kingdom.
  • Rowe JB; UCL Institute for Liver and Digestive Health, Royal Free Hospital and UCL, London, United Kingdom.
  • Gerhard A; Department of Clinical Neurosciences, University of Cambridge and Cambridge University Hospitals Trust, Cambridge, United Kingdom.
  • Butler CR; Division of Neuroscience and Experimental Psychology, Wolfson Molecular Imaging Centre, University of Manchester, Manchester, United Kingdom.
  • Masellis M; Departments of Geriatric Medicine and Nuclear Medicine, University of Duisburg-Essen, Duisburg, Germany.
  • Bremner F; Department of Brain Sciences, Imperial College London, London, United Kingdom.
  • Martin A; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
  • Jung L; Departamento de Neurología, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Cook P; Sunnybrook Health Sciences Centre, Sunnybrook Research Institute, University of Toronto, Toronto, Ontario, Canada.
  • Zetterberg H; Neuro-Ophthalmology, National Hospital for Neurology and Neurosurgery, London, United Kingdom.
  • Bandmann O; Department of Clinical Chemistry, Northern General Hospital, Sheffield, United Kingdom.
  • Rohrer JD; Department of Clinical Biochemistry, Southampton General Hospital, Southampton, United Kingdom.
  • Warner TT; Department of Clinical Biochemistry, Southampton General Hospital, Southampton, United Kingdom.
Mov Disord ; 36(2): 503-508, 2021 02.
Article in En | MEDLINE | ID: mdl-33078859
BACKGROUND: Outcomes are unpredictable for neurological presentations of Wilson's disease (WD). Dosing regimens for chelation therapy vary and monitoring depends on copper indices, which do not reflect end-organ damage. OBJECTIVE: To identify a biomarker for neurological involvement in WD. METHODS: Neuronal and glial-specific proteins were measured in plasma samples from 40 patients and 38 age-matched controls. Patients were divided into neurological or hepatic presentations and those with recent neurological presentations or deterioration associated with non-adherence were subcategorized as having active neurological disease. Unified WD Rating Scale scores and copper indices were recorded. RESULTS: Unlike copper indices, neurofilament light (NfL) concentrations were higher in neurological than hepatic presentations. They were also higher in those with active neurological disease when controlling for severity and correlated with neurological examination subscores in stable patients. CONCLUSION: NfL is a biomarker of neurological involvement with potential use in guiding chelation therapy and clinical trials for novel treatments. © 2020 University College London. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatolenticular Degeneration Type of study: Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2021 Document type: Article Affiliation country: United kingdom Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatolenticular Degeneration Type of study: Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2021 Document type: Article Affiliation country: United kingdom Country of publication: United States