Cortical and subcortical grey matter atrophy in Amyotrophic Lateral Sclerosis correlates with measures of disease accumulation independent of disease aggressiveness.


Journal

NeuroImage. Clinical
ISSN: 2213-1582
Titre abrégé: Neuroimage Clin
Pays: Netherlands
ID NLM: 101597070

Informations de publication

Date de publication:
2022
Historique:
received: 30 01 2022
revised: 11 07 2022
accepted: 18 08 2022
pubmed: 7 9 2022
medline: 15 12 2022
entrez: 6 9 2022
Statut: ppublish

Résumé

There is a growing demand for reliable biomarkers to monitor disease progression in Amyotrophic Lateral Sclerosis (ALS) that also take the heterogeneity of ALS into account. In this study, we explored the association between Magnetic Resonance Imaging (MRI)-derived measures of cortical thickness (CT) and subcortical grey matter (GM) volume with D50 model parameters. T1-weighted MRI images of 72 Healthy Controls (HC) and 100 patients with ALS were analyzed using Surface-based Morphometry for cortical structures and Voxel-based Morphometry for subcortical Region-Of-Interest analyses using the Computational Anatomy Toolbox (CAT12). In Inter-group contrasts, these parameters were compared between patients and HC. Further, the D50 model was used to conduct subgroup-analyses, dividing patients by a) Phase of disease covered at the time of MRI-scan and b) individual overall disease aggressiveness. Finally, correlations between GM and D50 model-derived parameters were examined. Inter-group analyses revealed ALS-related cortical thinning compared to HC located mainly in frontotemporal regions and a decrease in GM volume in the left hippocampus and amygdala. A comparison of patients in different phases showed further cortical and subcortical GM atrophy along with disease progression. Correspondingly, regression analyses identified negative correlations between cortical thickness and individual disease covered. However, there were no differences in CT and subcortical GM between patients with low and high disease aggressiveness. By application of the D50 model, we identified correlations between cortical and subcortical GM atrophy and ALS-related functional disability, but not with disease aggressiveness. This qualifies CT and subcortical GM volume as biomarkers representing individual disease covered to monitor therapeutic interventions in ALS.

Identifiants

pubmed: 36067613
pii: S2213-1582(22)00227-3
doi: 10.1016/j.nicl.2022.103162
pmc: PMC9460837
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103162

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Nora Dieckmann (N)

Department of Neurology, University Hospital Jena, Jena, Germany.

Annekathrin Roediger (A)

Department of Neurology, University Hospital Jena, Jena, Germany.

Tino Prell (T)

Department of Geriatrics, University Hospital Halle, Halle, Germany.

Simon Schuster (S)

Precision Neurology, University of Lübeck, Luebeck, Germany.

Meret Herdick (M)

Precision Neurology, University of Lübeck, Luebeck, Germany.

Thomas E Mayer (TE)

Department of Neuroradiology, University Hospital Jena, Jena, Germany.

Otto W Witte (OW)

Department of Neurology, University Hospital Jena, Jena, Germany.

Robert Steinbach (R)

Department of Neurology, University Hospital Jena, Jena, Germany. Electronic address: Robert.Steinbach@med.uni-jena.de.

Julian Grosskreutz (J)

Precision Neurology, University of Lübeck, Luebeck, Germany.

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Classifications MeSH