Neurogenetic traits outline vulnerability to cortical disruption in Parkinson’s disease

The genetic traits that underlie vulnerability to neuronal damage across specific brain circuits in Parkinson’s disease (PD) remain to be elucidated. In this study, we characterized the brain topological intersection between propagating connectivity networks in controls and PD participants and gene...

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Autores: Basaia, S. (Silvia)|||/items/cd793d81-3221-4656-8a65-809849b8dd63, Agosta, F. (Federica)|||/items/6f2f430b-eba8-41e3-9942-67cbe06b03ee, Diez, I. (Ibai)|||/items/86905c33-fa56-4bdb-8c83-6c521a1764b6, Bueichekú, E. (Elisenda)|||/items/813acf6f-b593-46cb-9e8a-8525fedcd91e, d’Oleire-Uquillas, F. (Federico)|||/items/e21a1a80-2932-4632-91ee-b217b95d175d, Delgado-Alvarado, M. (Manuel)|||/items/a4951956-75a5-4b50-872b-6291081c0681, Caballero-Gaudes, C. (César)|||/items/64b32c36-8f36-497b-ae62-2b2956f483ad, Rodriguez-Oroz, M.C. (María Cruz)|||/items/ba71432e-1a59-4a6d-87af-ba74627ba030, Stojkovic, T. (Tanja)|||/items/0c0897ed-26c5-4de8-8b24-fe3426d12722, Kostic, V. (Vladimir)|||/items/9433ca57-244c-44ca-a2c6-480bf6eb15ec, Filippi, M. (Massimo)|||/items/ff8ee205-779d-4a57-a968-7047340fac42, Sepulcre, J. (Jorge)|||/items/f0581de0-92ca-48ca-9154-f9704cf6a5fc
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/119715
Acceso en línea:https://hdl.handle.net/10171/119715
Access Level:acceso abierto
Palabra clave:Parkinson’s disease
fMRI
Connectomics
Cortical
Gene
Expression
Descripción
Sumario:The genetic traits that underlie vulnerability to neuronal damage across specific brain circuits in Parkinson’s disease (PD) remain to be elucidated. In this study, we characterized the brain topological intersection between propagating connectivity networks in controls and PD participants and gene expression patterns across the human cortex – such as the SNCA gene. We observed that brain connectivity originated from PD-related pathology epicenters in the brainstem recapitulated the anatomical distribution of alpha-synuclein histopathology in postmortem data. We also discovered that the gene set most related to cortical propagation patterns of PDrelated pathology was primarily involved in microtubule cellular components. Thus, this study sheds light on new avenues for enhancing detection of PD neuronal vulnerability via an evaluation of in vivo connectivity trajectories across the human brain and successful integration of neuroimaging-genetic strategies.