Phenotypic categorisation of individual subjects with motor neuron disease based on radiological disease burden patterns: A machine-learning approach.

Amyotrophic lateral sclerosis Artificial neural networks Biomarkers Clinical trials Diffusion imaging Machine-learning Motor neuron disease Neuroimaging Primary lateral sclerosis

Journal

Journal of the neurological sciences
ISSN: 1878-5883
Titre abrégé: J Neurol Sci
Pays: Netherlands
ID NLM: 0375403

Informations de publication

Date de publication:
15 Jan 2022
Historique:
received: 16 11 2021
revised: 25 11 2021
accepted: 29 11 2021
pubmed: 8 12 2021
medline: 29 1 2022
entrez: 7 12 2021
Statut: ppublish

Résumé

Motor neuron disease is an umbrella term encompassing a multitude of clinically heterogeneous phenotypes. The early and accurate categorisation of patients is hugely important, as MND phenotypes are associated with markedly different prognoses, progression rates, care needs and benefit from divergent management strategies. The categorisation of patients shortly after symptom onset is challenging, and often lengthy clinical monitoring is needed to assign patients to the appropriate phenotypic subgroup. In this study, a multi-class machine-learning strategy was implemented to classify 300 patients based on their radiological profile into diagnostic labels along the UMN-LMN spectrum. A comprehensive panel of cortical thickness measures, subcortical grey matter variables, and white matter integrity metrics were evaluated in a multilayer perceptron (MLP) model. Additional exploratory analyses were also carried out using discriminant function analyses (DFA). Excellent classification accuracy was achieved for amyotrophic lateral sclerosis in the testing cohort (93.7%) using the MLP model, but poor diagnostic accuracy was detected for primary lateral sclerosis (43.8%) and poliomyelitis survivors (60%). Feature importance analyses highlighted the relevance of white matter diffusivity metrics and the evaluation of cerebellar indices, cingulate measures and thalamic radiation variables to discriminate MND phenotypes. Our data suggest that radiological data from single patients may be meaningfully interpreted if large training data sets are available and the provision of diagnostic probability outcomes may be clinically useful in patients with short symptom duration. The computational interpretation of multimodal radiology datasets herald viable diagnostic, prognostic and clinical trial applications.

Identifiants

pubmed: 34875472
pii: S0022-510X(21)02781-7
doi: 10.1016/j.jns.2021.120079
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

120079

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Peter Bede (P)

Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland; Pitié-Salpêtrière University Hospital, Sorbonne University, Paris, France. Electronic address: bedep@tcd.ie.

Aizuri Murad (A)

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

Jasmin Lope (J)

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

Stacey Li Hi Shing (S)

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

Eoin Finegan (E)

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

Rangariroyashe H Chipika (RH)

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

Orla Hardiman (O)

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

Kai Ming Chang (KM)

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

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