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Phenotypic categorisation of individual subjects with motor neuron disease based on radiological disease burden patterns: A machine-learning approach.
Bede, Peter; Murad, Aizuri; Lope, Jasmin; Li Hi Shing, Stacey; Finegan, Eoin; Chipika, Rangariroyashe H; Hardiman, Orla; Chang, Kai Ming.
Afiliación
  • 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.
  • Murad A; Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland.
  • Lope J; Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland.
  • Li Hi Shing S; Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland.
  • Finegan E; Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland.
  • Chipika RH; Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland.
  • Hardiman O; Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland.
  • Chang KM; Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland; Department of Electronics and Computer Science, University of Southampton, UK.
J Neurol Sci ; 432: 120079, 2022 Jan 15.
Article en En | MEDLINE | ID: mdl-34875472
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Radiología / Enfermedad de la Neurona Motora / Esclerosis Amiotrófica Lateral Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Neurol Sci Año: 2022 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Radiología / Enfermedad de la Neurona Motora / Esclerosis Amiotrófica Lateral Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Neurol Sci Año: 2022 Tipo del documento: Article Pais de publicación: Países Bajos