In vivo cholinergic basal forebrain degeneration and cognition in Parkinson's disease : Imaging results from the COPPADIS study

Michel J. Grothe, Miguel A. Labrador-Espinosa, Silvia Jesús Maestre, Daniel Macías-García, A.D Adarmes-Gómez, Fátima Carrillo, Elena Iglesias Camacho, Pablo Franco-Rosado, Florinda Roldán Lora, Juan Francisco Martín-Rodríguez, Miquel Aguilar Barberà, Pau Pastor, Sonia Escalante Arroyo, Berta Soriano Vila, Anna Cots-Foraster, Javier Ruiz Martínez, Francisco Carrillo Padilla, Mercedes Pueyo Morlans, Isabel Gonzalez-Aramburu, Jon Infante CeberioJorge Hernández Vara, Oriol de Fàbregues-Boixar i Nebot, Teresa de Deus Fonticoba, Berta María Pascual-Sedano, Jaime Kulisevsky, Pablo Martínez-Martín, Diego Santos García, Pablo Mir

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Resumen

Introduction: We aimed to assess associations between multimodal neuroimaging measures of cholinergic basal forebrain (CBF) integrity and cognition in Parkinson's disease (PD) without dementia. Methods: The study included a total of 180 non-demented PD patients and 45 healthy controls, who underwent structural MRI acquisitions and standardized neurocognitive assessment through the PD-Cognitive Rating Scale (PD-CRS) within the multicentric COPPADIS-2015 study. A subset of 73 patients also had Diffusion Tensor Imaging (DTI) acquisitions. Volumetric and microstructural (mean diffusivity, MD) indices of CBF degeneration were automatically extracted using a stereotactic CBF atlas. For comparison, we also assessed multimodal indices of hippocampal degeneration. Associations between imaging measures and cognitive performance were assessed using linear models. Results: Compared to controls, CBF volume was not significantly reduced in PD patients as a group. However, across PD patients lower CBF volume was significantly associated with lower global cognition (PD-CRS: r = 0.37, p < 0.001), and this association remained significant after controlling for several potential confounding variables (p = 0.004). Analysis of individual item scores showed that this association spanned executive and memory domains. No analogue cognition associations were observed for CBF MD. In covariate-controlled models, hippocampal volume was not associated with cognition in PD, but there was a significant association for hippocampal MD (p = 0.02). Conclusions: Early cognitive deficits in PD without dementia are more closely related to structural MRI measures of CBF degeneration than hippocampal degeneration. In our multicentric imaging acquisitions, DTI-based diffusion measures in the CBF were inferior to standard volumetric assessments for capturing cognition-relevant changes in non-demented PD.
Idioma originalInglés
Páginas (desde-hasta)0068-75
Número de páginas8
PublicaciónParkinsonism and Related Disorders
Volumen88
DOI
EstadoPublicada - 2021

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