Extra-motor cerebral changes and manifestations in primary lateral sclerosis.


Journal

Brain imaging and behavior
ISSN: 1931-7565
Titre abrégé: Brain Imaging Behav
Pays: United States
ID NLM: 101300405

Informations de publication

Date de publication:
Oct 2021
Historique:
accepted: 12 11 2020
pubmed: 8 1 2021
medline: 13 10 2021
entrez: 7 1 2021
Statut: ppublish

Résumé

Primary lateral sclerosis (PLS) is classically considered a 'pure' upper motor neuron disorder. Motor cortex atrophy and pyramidal tract degeneration are thought to be pathognomonic of PLS, but extra-motor cerebral changes are poorly characterized. In a prospective neuroimaging study, forty PLS patients were systematically evaluated with a standardised imaging, genetic and clinical protocol. Patients were screened for ALS and HSP associated mutations, as well as C9orf72 hexanucleotide repeats. Clinical assessment included composite reflex scores, spasticity scales, functional rating scales, and screening for cognitive and behavioural deficits. The neuroimaging protocol evaluated cortical atrophy patterns, subcortical grey matter changes and white matter alterations in whole-brain and region-of-interest analyses. PLS patients tested negative for known ALS- and HSP-associated mutations and C9orf72 repeat expansions. Voxel-wise analyses revealed anterior cingulate, dorsolateral prefrontal, insular, opercular, orbitofrontal and bilateral mesial temporal grey matter changes and white matter alterations in the fornix, brainstem, temporal lobes, and cerebellum. Significant thalamus, caudate, hippocampus, putamen and accumbens nucleus volume reductions were also identified. Extra-motor clinical manifestations were dominated by verbal fluency deficits, language deficits, apathy and pseudobulbar affect. Our clinical and radiological evaluation confirms considerable extra-motor changes in a population-based cohort of PLS patients. Our data suggest that PLS should no longer be considered a neurodegenerative disorder selectively affecting the pyramidal system. PLS is associated with widespread extra-motor changes and manifestations which should be carefully considered in the multidisciplinary management of this low-incidence condition.

Identifiants

pubmed: 33409820
doi: 10.1007/s11682-020-00421-4
pii: 10.1007/s11682-020-00421-4
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2283-2296

Subventions

Organisme : Health Research Board Ireland
ID : HRB EIA-2017-019

Informations de copyright

© 2021. Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Eoin Finegan (E)

Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.

Stacey Li Hi Shing (SLH)

Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.

Rangariroyashe H Chipika (RH)

Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.

Kai Ming Chang (KM)

Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.
Electronics and Computer Science, University of Southampton, Southampton, UK.

Mary Clare McKenna (MC)

Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.

Mark A Doherty (MA)

Complex Trait Genomics Laboratory, Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.

Jennifer C Hengeveld (JC)

Complex Trait Genomics Laboratory, Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.

Alice Vajda (A)

Complex Trait Genomics Laboratory, Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.

Niall Pender (N)

Department of Psychology, Beaumont Hospital, Dublin, Ireland.

Colette Donaghy (C)

Department of Neurology, Belfast, Western Health & Social Care Trust, Belfast, Northern Ireland.

Siobhan Hutchinson (S)

Department of Neurology, St James's Hospital, Dublin, Ireland.

Russell L McLaughlin (RL)

Complex Trait Genomics Laboratory, Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.

Orla Hardiman (O)

Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.

Peter Bede (P)

Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland. bedep@tcd.ie.

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