Identification of rare cortical folding patterns using unsupervised deep learning

Author:

Guillon Louise1,Chavas Joël1,Bénézit Audrey2,Moutard Marie-Laure3,Roca Pauline456,Mellerio Charles457,Oppenheim Catherine45,Rivière Denis1,Mangin Jean-François1

Affiliation:

1. CEA, CNRS, NeuroSpin, Baobab, Université Paris-Saclay, Gif-sur-Yvette, France

2. Service de Neurologie et Réanimation Pédiatrique, Hôpital Raymond Poincaré, APHP, Garches, France

3. Service de Neuropédiatrie, Hôpital Trousseau, Hôpitaux Universitaires de l’Est Parisien, Sorbonne Université, Paris, France

4. Institut de Psychiatrie et Neurosciences de Paris (IPNP), INSERM, UMR S1266, Université de Paris, Paris, France

5. Imaging Department, Groupe Hospitalier Universitaire Paris Psychiatrie et Neurosciences, Sainte-Anne Hospital, Paris, France

6. Pixyl, Research and Development Laboratory, Grenoble, France

7. Centre d’imagerie du Nord, Saint Denis, France

Abstract

Abstract Like fingerprints, cortical folding patterns are unique to each brain even though they follow a general species-specific organization. Some folding patterns have been linked with neurodevelopmental disorders. However, due to the high inter-individual variability, the identification of rare folding patterns that could become biomarkers remains a very complex task. This paper proposes a novel unsupervised deep learning approach to identify rare folding patterns and assess the degree of deviations that can be detected. To this end, we preprocess the brain MR images to focus the learning on the folding morphology and train a beta variational auto-encoder (β−VAE) on the inter-individual variability of the folding to identify outliers. We compare the detection power of the latent space and of the reconstruction errors, using synthetic benchmarks and one actual rare configuration related to the central sulcus. Finally, we assess the generalization of our method on a developmental anomaly located in another region and we validate the relevance of our approach on patients suffering from drug-resistant epilepsy. Our results suggest that this method enables encoding relevant folding characteristics that can be enlightened and better interpreted based on the generative power of the β−VAE. The latent space and the reconstruction errors bring complementary information and enable the identification of rare patterns of different nature. This method generalizes well to a different region on another dataset and demonstrates promising results on the epileptic patients. Code is available at https://github.com/neurospin-projects/2022_lguillon_rare_folding_detection.

Publisher

MIT Press

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