Multiparametric Microstructural MRI and Machine Learning Classification Yields High Diagnostic Accuracy in Amyotrophic Lateral Sclerosis: Proof of Concept.

amyotrophic lateral sclerosis diffusion tensor imaging (DTI) machine learning magnetic resonance imaging (MRI) motor neuron disease neural network neurodegeneration support vector machine (SVM)

Journal

Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899

Informations de publication

Date de publication:
2021
Historique:
received: 22 07 2021
accepted: 21 10 2021
entrez: 6 12 2021
pubmed: 7 12 2021
medline: 7 12 2021
Statut: epublish

Résumé

The potential of multiparametric quantitative neuroimaging has been extensively discussed as a diagnostic tool in amyotrophic lateral sclerosis (ALS). In the past, the integration of multimodal, quantitative data into a useful diagnostic classifier was a major challenge. With recent advances in the field, machine learning in a data driven approach is a potential solution: neuroimaging biomarkers in ALS are mainly observed in the cerebral microstructure, with diffusion tensor imaging (DTI) and texture analysis as promising approaches. We set out to combine these neuroimaging markers as age-corrected features in a machine learning model with a cohort of 502 subjects, divided into 404 patients with ALS and 98 healthy controls. We calculated a linear support vector classifier (SVC) which is a very robust model and then verified the results with a multilayer perceptron (MLP)/neural network. Both classifiers were able to separate ALS patients from controls with receiver operating characteristic (ROC) curves showing an area under the curve (AUC) of 0.87-0.88 ("good") for the SVC and 0.88-0.91 ("good" to "excellent") for the MLP. Among the coefficients of the SVC, texture data contributed the most to a correct classification. We consider these results as a proof of concept that demonstrated the power of machine learning in the application of multiparametric quantitative neuroimaging data to ALS.

Identifiants

pubmed: 34867726
doi: 10.3389/fneur.2021.745475
pmc: PMC8637840
doi:

Types de publication

Journal Article

Langues

eng

Pagination

745475

Informations de copyright

Copyright © 2021 Kocar, Behler, Ludolph, Müller and Kassubek.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Thomas D Kocar (TD)

Department of Neurology, University of Ulm, Ulm, Germany.

Anna Behler (A)

Department of Neurology, University of Ulm, Ulm, Germany.

Albert C Ludolph (AC)

Department of Neurology, University of Ulm, Ulm, Germany.
German Center for Neurodegenerative Diseases (DZNE), Ulm, Germany.

Hans-Peter Müller (HP)

Department of Neurology, University of Ulm, Ulm, Germany.

Jan Kassubek (J)

Department of Neurology, University of Ulm, Ulm, Germany.
German Center for Neurodegenerative Diseases (DZNE), Ulm, Germany.

Classifications MeSH