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Automated Categorization of Parkinsonian Syndromes Using Magnetic Resonance Imaging in a Clinical Setting.
Chougar, Lydia; Faouzi, Johann; Pyatigorskaya, Nadya; Yahia-Cherif, Lydia; Gaurav, Rahul; Biondetti, Emma; Villotte, Marie; Valabrègue, Romain; Corvol, Jean-Christophe; Brice, Alexis; Mariani, Louise-Laure; Cormier, Florence; Vidailhet, Marie; Dupont, Gwendoline; Piot, Ines; Grabli, David; Payan, Christine; Colliot, Olivier; Degos, Bertrand; Lehéricy, Stéphane.
Afiliación
  • Chougar L; Paris Brain Institute-ICM, INSERM U 1127, CNRS UMR 7225, Sorbonne Université, UMR S 1127, CNRS UMR 7225, Paris, France.
  • Faouzi J; ICM, "Movement Investigations and Therapeutics" Team (MOV'IT), Paris, France.
  • Pyatigorskaya N; ICM, Centre de NeuroImagerie de Recherche-CENIR, Paris, France.
  • Yahia-Cherif L; Department of Neuroradiology, Pitié-Salpêtrière University Hospital, APHP, Paris, France.
  • Gaurav R; Paris Brain Institute-ICM, INSERM U 1127, CNRS UMR 7225, Sorbonne Université, UMR S 1127, CNRS UMR 7225, Paris, France.
  • Biondetti E; INRIA, Aramis Team, Paris, France.
  • Villotte M; Paris Brain Institute-ICM, INSERM U 1127, CNRS UMR 7225, Sorbonne Université, UMR S 1127, CNRS UMR 7225, Paris, France.
  • Valabrègue R; ICM, "Movement Investigations and Therapeutics" Team (MOV'IT), Paris, France.
  • Corvol JC; ICM, Centre de NeuroImagerie de Recherche-CENIR, Paris, France.
  • Brice A; Department of Neuroradiology, Pitié-Salpêtrière University Hospital, APHP, Paris, France.
  • Mariani LL; Paris Brain Institute-ICM, INSERM U 1127, CNRS UMR 7225, Sorbonne Université, UMR S 1127, CNRS UMR 7225, Paris, France.
  • Cormier F; ICM, Centre de NeuroImagerie de Recherche-CENIR, Paris, France.
  • Vidailhet M; Paris Brain Institute-ICM, INSERM U 1127, CNRS UMR 7225, Sorbonne Université, UMR S 1127, CNRS UMR 7225, Paris, France.
  • Dupont G; ICM, "Movement Investigations and Therapeutics" Team (MOV'IT), Paris, France.
  • Piot I; ICM, Centre de NeuroImagerie de Recherche-CENIR, Paris, France.
  • Grabli D; Paris Brain Institute-ICM, INSERM U 1127, CNRS UMR 7225, Sorbonne Université, UMR S 1127, CNRS UMR 7225, Paris, France.
  • Payan C; ICM, "Movement Investigations and Therapeutics" Team (MOV'IT), Paris, France.
  • Colliot O; ICM, Centre de NeuroImagerie de Recherche-CENIR, Paris, France.
  • Degos B; Faculté de Médecine, Université Denis Diderot, Paris, France.
  • Lehéricy S; Paris Brain Institute-ICM, INSERM U 1127, CNRS UMR 7225, Sorbonne Université, UMR S 1127, CNRS UMR 7225, Paris, France.
Mov Disord ; 36(2): 460-470, 2021 02.
Article en En | MEDLINE | ID: mdl-33137232
BACKGROUND: Machine learning algorithms using magnetic resonance imaging (MRI) data can accurately discriminate parkinsonian syndromes. Validation in patients recruited in routine clinical practice is missing. OBJECTIVE: The aim of this study was to assess the accuracy of a machine learning algorithm trained on a research cohort and tested on an independent clinical replication cohort for the categorization of parkinsonian syndromes. METHODS: Three hundred twenty-two subjects, including 94 healthy control subjects, 119 patients with Parkinson's disease (PD), 51 patients with progressive supranuclear palsy (PSP) with Richardson's syndrome, 35 with multiple system atrophy (MSA) of the parkinsonian variant (MSA-P), and 23 with MSA of the cerebellar variant (MSA-C), were recruited. They were divided into a training cohort (n = 179) scanned in a research environment and a replication cohort (n = 143) examined in clinical practice on different MRI systems. Volumes and diffusion tensor imaging (DTI) metrics in 13 brain regions were used as input for a supervised machine learning algorithm. To harmonize data across scanners and reduce scanner-dependent effects, we tested two types of normalizations using patient data or healthy control data. RESULTS: In the replication cohort, high accuracies were achieved using volumetry in the classification of PD-PSP, PD-MSA-C, PSP-MSA-C, and PD-atypical parkinsonism (balanced accuracies: 0.840-0.983, area under the receiver operating characteristic curves: 0.907-0.995). Performances were lower for the classification of PD-MSA-P, MSA-C-MSA-P (balanced accuracies: 0.765-0.784, area under the receiver operating characteristic curve: 0.839-0.871) and PD-PSP-MSA (balanced accuracies: 0.773). Performance using DTI was improved when normalizing by controls, but remained lower than that using volumetry alone or combined with DTI. CONCLUSIONS: A machine learning approach based on volumetry enabled accurate classification of subjects with early-stage parkinsonism, examined on different MRI systems, as part of their clinical assessment. © 2020 International Parkinson and Movement Disorder Society.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Parálisis Supranuclear Progresiva / Atrofia de Múltiples Sistemas / Trastornos Parkinsonianos Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Parálisis Supranuclear Progresiva / Atrofia de Múltiples Sistemas / Trastornos Parkinsonianos Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Francia