Literature DB >> 34875472

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

Peter Bede1, Aizuri Murad2, Jasmin Lope2, Stacey Li Hi Shing2, Eoin Finegan2, Rangariroyashe H Chipika2, Orla Hardiman2, Kai Ming Chang3.   

Abstract

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

Entities:  

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

Mesh:

Year:  2021        PMID: 34875472     DOI: 10.1016/j.jns.2021.120079

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  2 in total

Review 1.  Pre-symptomatic radiological changes in frontotemporal dementia: propagation characteristics, predictive value and implications for clinical trials.

Authors:  Mary Clare McKenna; Jasmin Lope; Ee Ling Tan; Peter Bede
Journal:  Brain Imaging Behav       Date:  2022-08-03       Impact factor: 3.224

2.  Clusters of anatomical disease-burden patterns in ALS: a data-driven approach confirms radiological subtypes.

Authors:  Peter Bede; Aizuri Murad; Jasmin Lope; Orla Hardiman; Kai Ming Chang
Journal:  J Neurol       Date:  2022-03-25       Impact factor: 6.682

  2 in total

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