Deep Learning to Differentiate Parkinsonian Syndromes Using Multimodal Magnetic Resonance Imaging: A Proof‐of‐Concept Study

Giulia Maria Mattia, Lydia Chougar, Alexandra Foubert‐Samier, Wassilios G. Meissner, Margherita Fabbri, Anne Pavy‐Le Traon, Olivier Rascol, David Grabli, Bertrand Degos, Nadya Pyatigorskaya, Alice Faucher, Marie Vidailhet, Jean‐Christophe Corvol, Stéphane Lehéricy, Patrice Péran
Movement Disorders. 2025-07-24; :
DOI: 10.1002/mds.30300

PubMed
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https://www.bordeaux-neurocampus.fr/11921

AbstractBackgroundThe differentiation between multiple system atrophy (MSA) and Parkinson’s disease (PD) based on clinical diagnostic criteria can be challenging, especially at an early stage. Leveraging deep learning methods and magnetic resonance imaging (MRI) data has shown great potential in aiding automatic diagnosis.ObjectiveThe aim was to determine the feasibility of a three‐dimensional convolutional neural network (3D CNN)–based approach using multimodal, multicentric MRI data for differentiating MSA and its variants from PD.MethodsMRI data were retrospectively collected from three MSA French reference centers. We computed quantitative maps of gray matter density (GD) from a T1‐weighted sequence and mean diffusivity (MD) from diffusion tensor imaging. These maps were used as input to a 3D CNN, either individually (“monomodal,” “GD” or “MD”) or in combination (“bimodal,” “GD‐MD”). Classification tasks included the differentiation of PD and MSA patients. Model interpretability was investigated by analyzing misclassified patients and providing a visual interpretation of the most activated regions in CNN predictions.ResultsThe study population included 92 patients with MSA (50 with MSA‐P, parkinsonian variant; 33 with MSA‐C, cerebellar variant; 9 with MSA‐PC, mixed variant) and 64 with PD. The best accuracies were obtained for the PD/MSA (0.88 ± 0.03 with GD‐MD), PD/MSA‐C&PC (0.84 ± 0.08 with MD), and PD/MSA‐P (0.78 ± 0.09 with GD) tasks. Patients misclassified by the CNN exhibited fewer and milder image alterations, as found using an image‐based z score analysis. Activation maps highlighted regions involved in MSA pathophysiology, namely the putamen and cerebellum.ConclusionsOur findings hold promise for developing an efficient, MRI‐based, and user‐independent diagnostic tool suitable for differentiating parkinsonian syndromes in clinical practice. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Auteurs Bordeaux Neurocampus