Spatial analysis of paraneoplastic cerebellar degeneration in ovarian cancer with anti-Yo syndrome and SCA1.
Authors
Affiliations (8)
Affiliations (8)
- ICM, INSERM U 1127, CNRS UMR 7225, UMRS 1127, Paris Brain Institute, Sorbonne University, Paris, France.
- Neurological Department, Groupe Hospitalier Paris Saint-Joseph, Paris, France.
- Université Paris Cité, Paris, France.
- Charles Foix, DMU Neurosciences, Service de Neuro-Oncologie-Institut de Neurologie, AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière, Paris, France.
- Department of Neuroradiology, APHP, La Pitié-Salpêtrière Hospital, Sorbonne University, F-75013, Paris, France.
- APHP-Salpêtrière Hospital, DMU BioGem, CNRS, INSERM, Paris Brain Institute, Sorbonne University, Paris, France.
- ICM, INSERM U 1127, CNRS UMR 7225, UMRS 1127, Paris Brain Institute, Sorbonne University, Paris, France. [email protected].
- Charles Foix, DMU Neurosciences, Service de Neuro-Oncologie-Institut de Neurologie, AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière, Paris, France. [email protected].
Abstract
Anti-Yo paraneoplastic cerebellar degeneration (PCD) is a rare autoimmune disorder linked to ovarian and breast cancers. Neurological symptoms often precede cancer diagnosis, yet conventional imaging techniques may fail to detect early cerebellar changes. This study quantitatively assessed cerebellar atrophy and network alterations in anti-Yo PCD patients compared to healthy controls and patients with spinocerebellar ataxia type 1 (SCA1). We analyzed structural MRI data from 11 antiYo PCD patients, 17 healthy controls, and 17 SCA1 patients. Cerebellar lobular segmentation and cortical thickness measurements were conducted. Structural covariance networks were built using inter-lobular Pearson correlation coefficients (threshold |r| > 0.5), with graph theory metrics assessing connectivity. Univariate and age-adjusted multivariate analyses evaluated group differences, and machine learning assessed the discriminative power of regional morphometric measures. AntiYo PCD patients showed pronounced anterior cortical thinning, while SCA1 atrophy was milder and more posterior. Two PCD subtypes emerged: one with severe atrophy, another with nearnormal thickness. Network analysis revealed increased node strength and clustering coefficients, but reduced betweenness centrality in PCD, suggesting altered network hierarchy and widespread clustering that may reflect pathological reorganization. In cross-validated analysis, regional cerebellar features distinguished PCD, SCA1, and controls with promising AUC values. Anti-Yo PCD is characterized by anterior cerebellar vulnerability and network reorganization distinct from SCA1. These morphometric and connectivity markers are candidate imaging biomarkers for early diagnosis and subgroup stratification in paraneoplastic cerebellar degeneration.