Publication:
Neurogenetic traits outline vulnerability to cortical disruption in Parkinson's disease

dc.contributor.authorBasaia, Silvia (56830447300)
dc.contributor.authorAgosta, Federica (6701687853)
dc.contributor.authorDiez, Ibai (56673934700)
dc.contributor.authorBueichekú, Elisenda (56502262000)
dc.contributor.authord'Oleire Uquillas, Federico (56663302500)
dc.contributor.authorDelgado-Alvarado, Manuel (55382885300)
dc.contributor.authorCaballero-Gaudes, César (6506596377)
dc.contributor.authorRodriguez-Oroz, MariCruz (6602886527)
dc.contributor.authorStojkovic, Tanja (57211211787)
dc.contributor.authorKostic, Vladimir S. (35239923400)
dc.contributor.authorFilippi, Massimo (7202268530)
dc.contributor.authorSepulcre, Jorge (14829519300)
dc.date.accessioned2025-06-12T13:06:08Z
dc.date.available2025-06-12T13:06:08Z
dc.date.issued2022
dc.description.abstractThe 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 PD-related 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. © 2022 The Author(s)
dc.identifier.urihttps://doi.org/10.1016/j.nicl.2022.102941
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85123372897&doi=10.1016%2fj.nicl.2022.102941&partnerID=40&md5=882708dc251aa5529258706987fb591a
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/3813
dc.subjectConnectomics
dc.subjectCortical Gene Expression
dc.subjectfMRI
dc.subjectParkinson's disease
dc.titleNeurogenetic traits outline vulnerability to cortical disruption in Parkinson's disease
dspace.entity.typePublication

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