The role of neurofilament light in genetic frontotemporal lobar degeneration.

disease progression frontotemporal dementia frontotemporal lobar degeneration neurofilament light trial stratification

Journal

Brain communications
ISSN: 2632-1297
Titre abrégé: Brain Commun
Pays: England
ID NLM: 101755125

Informations de publication

Date de publication:
2023
Historique:
received: 16 06 2022
revised: 26 09 2022
accepted: 23 11 2022
entrez: 25 1 2023
pubmed: 26 1 2023
medline: 26 1 2023
Statut: epublish

Résumé

Genetic frontotemporal lobar degeneration caused by autosomal dominant gene mutations provides an opportunity for targeted drug development in a highly complex and clinically heterogeneous dementia. These neurodegenerative disorders can affect adults in their middle years, progress quickly relative to other dementias, are uniformly fatal and have no approved disease-modifying treatments. Frontotemporal dementia, caused by mutations in the

Identifiants

pubmed: 36694576
doi: 10.1093/braincomms/fcac310
pii: fcac310
pmc: PMC9866262
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

fcac310

Subventions

Organisme : Medical Research Council
ID : MR/M008525/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M023664/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T046015/1
Pays : United Kingdom

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the Guarantors of Brain.

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Auteurs

Henrik Zetterberg (H)

Department of Psychiatry and Neurochemistry, University of Gothenburg, Gothenburg, Sweden.
Clinical Chemistry, Sahlgrenska University Hospital, Gothenburg, Sweden.
Dementia Research Institute, University College London, London, UK.
DRI Fluid Biomarker Laboratory, Hong Kong Center for Neurodegenerative Diseases, Hong Kong, China.

Charlotte Teunissen (C)

Department of Clinical Chemistry, Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.

John van Swieten (J)

Department of Neurology, Erasmus Medical Center, Rotterdam, the Netherlands.

Jens Kuhle (J)

Department of Clinical Research, Department of Neurology, Department of Biomedicine, Multiple Sclerosis Centre, University Hospital Basel, University of Basel, Basel, Switzerland.

Adam Boxer (A)

Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, CA, USA.

Jonathan D Rohrer (JD)

Queen Square UCL Institute of Neurology, Dementia Research Centre, UK Dementia Research Institute, University College London, London, UK.

Laura Mitic (L)

Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, CA, USA.
The Bluefield Project to Cure FTD, San Francisco, CA, USA.

Alexandra M Nicholson (AM)

The Bluefield Project to Cure FTD, San Francisco, CA, USA.
Department of Neuroscience, Mayo Clinic Jacksonville, Jacksonville, FL, USA.

Rodney Pearlman (R)

The Bluefield Project to Cure FTD, San Francisco, CA, USA.

Stella Mayo McCaughey (SM)

Medical Affairs, Alector, Inc., South San Francisco, CA, USA.

Nadine Tatton (N)

Medical Affairs, Alector, Inc., South San Francisco, CA, USA.

Classifications MeSH