Brain atrophy pattern in de novo Parkinsons disease with probable RBD associated with cognitive impairment

Rapid eye movement sleep behavior disorder (RBD) is associated with high likelihood of prodromal Parkinson's disease (PD) and is common in de novo PD. It is associated with greater cognitive impairment and brain atrophy. However, the relation between structural brain characteristics and cogniti...

ver descrição completa

Detalhes bibliográficos
Autores: Oltra González, Javier, Uribe, Carme, Segura i Fàbregas, Bàrbara, Campabadal Delgado, Anna, Inguanzo, Anna, Monté Rubio, Gemma C., Pardo, Jèssica, Martí Domènech, Ma. Josep, Compta, Yaroslau, Valldeoriola Serra, Francesc, Junqué i Plaja, Carme, 1955-, Iranzo, Alex
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2022
País:España
Recursos:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/190789
Acesso em linha:https://hdl.handle.net/2445/190789
Access Level:acceso abierto
Palavra-chave:Malaltia de Parkinson
Malalties cerebrals
Trastorns del son
Trastorns de la cognició
Imatges per ressonància magnètica
Parkinson's disease
Brain diseases
Sleep disorders
Cognition disorders
Magnetic resonance imaging
Descrição
Resumo:Rapid eye movement sleep behavior disorder (RBD) is associated with high likelihood of prodromal Parkinson's disease (PD) and is common in de novo PD. It is associated with greater cognitive impairment and brain atrophy. However, the relation between structural brain characteristics and cognition remains poorly understood. We aimed to investigate subcortical and cortical atrophy in de novo PD with probable RBD (PD-pRBD) and to relate it with cognitive impairment. We analyzed volumetry, cortical thickness, and cognitive measures from 79 PD-pRBD patients, 126 PD without probable RBD patients (PD-non pRBD), and 69 controls from the Parkinson's Progression Markers Initiative (PPMI). Regression models of cognition were tested using magnetic resonance imaging measures as predictors. We found lower left thalamus volume in PD-pRBD compared with PD-non pRBD. Compared with controls, PD-pRBD group showed atrophy in the bilateral putamen, left hippocampus, left amygdala, and thinning in the right superior temporal gyrus. Specific deep gray matter nuclei volumes were associated with impairment in global cognition, phonemic fluency, processing speed, and visuospatial function in PD-pRBD. In conclusion, cognitive impairment and gray matter atrophy are already present in de novo PD-pRBD. Thalamus, hippocampus, and putamen volumes were mainly associated with these cognitive deficits.