Mismatch between clinically defined classification of ALS stage and the burden of cerebral pathology.

Amyotrophic lateral sclerosis Clinical classification Early stage Longitudinal analysis Magnetic resonance imaging Texture analysis

Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
28 Jan 2024
Historique:
received: 16 11 2023
accepted: 10 01 2024
revised: 05 01 2024
medline: 29 1 2024
pubmed: 29 1 2024
entrez: 28 1 2024
Statut: aheadofprint

Résumé

This study aimed to investigate the clinical stratification of amyotrophic lateral sclerosis (ALS) patients in relation to in vivo cerebral degeneration. One hundred forty-nine ALS patients and one hundred forty-four healthy controls (HCs) were recruited from the Canadian ALS Neuroimaging Consortium (CALSNIC). Texture analysis was performed on T1-weighted scans to extract the texture feature "autocorrelation" (autoc), an imaging biomarker of cerebral degeneration. Patients were stratified at baseline into early and advanced disease stages based on criteria adapted from ALS clinical trials and the King's College staging system, as well as into slow and fast progressors (disease progression rates, DPR). Patients had increased autoc in the internal capsule. These changes extended beyond the internal capsule in early-stage patients (clinical trial-based criteria), fast progressors, and in advanced-stage patients (King's staging criteria). Longitudinal increases in autoc were observed in the postcentral gyrus, corticospinal tract, posterior cingulate cortex, and putamen; whereas decreases were observed in corpus callosum, caudate, central opercular cortex, and frontotemporal areas. Both longitudinal increases and decreases of autoc were observed in non-overlapping regions within insula and precentral gyrus. Within-criteria comparisons of autoc revealed more pronounced changes at baseline and longitudinally in early- (clinical trial-based criteria) and advanced-stage (King's staging criteria) patients and fast progressors. In summary, comparative patterns of baseline and longitudinal progression in cerebral degeneration are dependent on sub-group selection criteria, with clinical trial-based stratification insufficiently characterizing disease stage based on pathological cerebral burden.

Identifiants

pubmed: 38282082
doi: 10.1007/s00415-024-12190-x
pii: 10.1007/s00415-024-12190-x
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

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Auteurs

Pedram Parnianpour (P)

Neuroscience and Mental Health Institute, University of Alberta, 562 Heritage Medical Research Centre, 11313-87 Ave, Edmonton, AB, T6G2S2, Canada. parnianp@ualberta.ca.

Michael Benatar (M)

Department of Neurology, University of Miami Miller School of Medicine, Miami, USA.

Hannah Briemberg (H)

Division of Neurology, University of British Columbia, Vancouver, BC, Canada.

Avyarthana Dey (A)

Neuroscience and Mental Health Institute, University of Alberta, 562 Heritage Medical Research Centre, 11313-87 Ave, Edmonton, AB, T6G2S2, Canada.

Annie Dionne (A)

Axe Neurosciences, CHU de Québec-Université Laval, Québec City, QC, Canada.
Department of Medicine, Faculty of Medicine, Université Laval, Quebec City, QC, Canada.

Nicolas Dupré (N)

Axe Neurosciences, CHU de Québec-Université Laval, Québec City, QC, Canada.
Department of Medicine, Faculty of Medicine, Université Laval, Quebec City, QC, Canada.

Karleyton C Evans (KC)

Biogen Inc., Cambridge, MA, USA.

Richard Frayne (R)

Hotchkiss Brain Institute, University of Calgary, Calgary, Canada.

Angela Genge (A)

Montreal Neurological Institute, McGill University, Montreal, Canada.

Simon J Graham (SJ)

Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.

Lawrence Korngut (L)

Hotchkiss Brain Institute, University of Calgary, Calgary, Canada.

Donald G McLaren (DG)

Vigil Neuroscience, Inc., Watertown, MA, USA.

Peter Seres (P)

Department of Biomedical Engineering, University of Alberta, Edmonton, Canada.

Robert C Welsh (RC)

Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.

Alan Wilman (A)

Department of Radiology and Diagnostic Imaging, University of Alberta, Edmonton, AB, Canada.

Lorne Zinman (L)

Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.

Sanjay Kalra (S)

Neuroscience and Mental Health Institute, University of Alberta, 562 Heritage Medical Research Centre, 11313-87 Ave, Edmonton, AB, T6G2S2, Canada.
Department of Biomedical Engineering, University of Alberta, Edmonton, Canada.
Division of Neurology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.

Classifications MeSH