Cerebellar dysfunction in frontotemporal dementia: intra-cerebellar pathology and cerebellar network degeneration

Our analyses capture significant cerebro-cerebellar disconnection in frontotemporal dementia. Corticospinal tract and motor cortex degeneration can be readily detected in non-ALS phenotypes. Intra-cerebellar pathology, coupled with the degeneration of cerebellar projections and the ensuing dysfunction of cerebro-cerebellar networks likely contribute to phenotype-defining clinical profiles in frontotemporal dementia. Infratentorial disease burden and cerebellar network dysfunction should, therefore, be carefully considered in FTD, and phenotype-defining neuropsychological profiles should not be solely attributed to supratentorial degeneration.

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Publication Details

Journal
Journal of Neurology
Published
2025-03-25
DOI
https://doi.org/10.1007/s00415-025-13046-8
Citations
3
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
4.17

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article

Cerebellar dysfunction in frontotemporal dementia: intra-cerebellar pathology and cerebellar network degeneration

Bernard L. Schneider, Cédric Raoul, Marlene Tahedl, Fabrice Ango et al.
3 citations
Journal of Neurology
Amyotrophic Lateral Sclerosis Research
4.17
article

Cerebellar dysfunction in frontotemporal dementia: intra-cerebellar pathology and cerebellar network degeneration

Bernard L. Schneider, Cédric Raoul, Marlene Tahedl, Fabrice Ango, Orla M. Hardiman, Mary C. McKenna, Siobhán Hutchinson, Peter Bede, Jana Kleinerová, Ee Ling Tan, Angela Garcia-Gallardo, Pierre‐François Pradat
article en
3 citations

Abstract

Our analyses capture significant cerebro-cerebellar disconnection in frontotemporal dementia. Corticospinal tract and motor cortex degeneration can be readily detected in non-ALS phenotypes. Intra-cerebellar pathology, coupled with the degeneration of cerebellar projections and the ensuing dysfunction of cerebro-cerebellar networks likely contribute to phenotype-defining clinical profiles in frontotemporal dementia. Infratentorial disease burden and cerebellar network dysfunction should, therefore, be carefully considered in FTD, and phenotype-defining neuropsychological profiles should not be solely attributed to supratentorial degeneration.

Journal of NeurologyVol. 272(4)
Centre National de la Recherche Scientifique (FR), Inserm (FR), Université de Montpellier (FR), Trinity College Dublin (IE), Sorbonne Université (FR), Laboratoire d’Imagerie Biomédicale (FR), Pitié-Salpêtrière Hospital (FR), Institute for Neurosciences of Montpellier (FR), St. James's Hospital (IE), École Polytechnique Fédérale de Lausanne (CH)
Health Research Board, EU Joint Programme – Neurodegenerative Disease Research, Irish Research eLibrary, Science Foundation Ireland, Agence Nationale de la Recherche
Openalex Percentile: Top 7%
Amyotrophic Lateral Sclerosis Research
4.17
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