Cortical Macro‐ and Microstructural Changes in Parkinson's Disease with Probable Rapid Eye Movement Sleep Behavior Disorder

Author:

Pardo Jèssica12ORCID,Montal Victor34ORCID,Campabadal Anna15ORCID,Oltra Javier12ORCID,Uribe Carme126ORCID,Roura Ignacio12ORCID,Bargalló Núria27ORCID,Martí Maria J.289ORCID,Compta Yaroslau289ORCID,Iranzo Alex2810ORCID,Fortea Juan3811ORCID,Junqué Carme128ORCID,Segura Bàrbara128ORCID

Affiliation:

1. Medical Psychology Unit, Department of Medicine Institute of Neurosciences, University of Barcelona Barcelona Spain

2. Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) Barcelona Spain

3. Sant Pau Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Universitat Autònoma de Barcelona Barcelona Spain

4. Department of Life Sciences Barcelona Supercomputing Center Barcelona Spain

5. Neurology Service, Consorci Corporació Sanitària Parc Taulí de Sabadell Barcelona Spain

6. Brain Health Imaging Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH) Toronto Ontario Canada

7. Imaging Diagnostic Center (CDI), Hospital Clínic Universitari de Barcelona Barcelona Spain

8. Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas Barcelona Spain

9. Parkinson's Disease and Movement Disorders Unit, Hospital Clínic Universitari de Barcelona, UBNeuro Institute of Neurosciences, University of Barcelona Barcelona Spain

10. Sleep Disorders Center, Neurology Service, Hospital Clínic Universitari de Barcelona, University of Barcelona Barcelona Spain

11. Barcelona Down Medical Center, Fundació Catalana de Síndrome de Down Barcelona Spain

Abstract

AbstractBackgroundEvidence regarding cortical atrophy patterns in Parkinson's disease (PD) with probable rapid eye movement sleep behavior disorder (RBD) (PD‐pRBD) remains scarce. Cortical mean diffusivity (cMD), as a novel imaging biomarker highly sensitive to detecting cortical microstructural changes in different neurodegenerative diseases, has not been investigated in PD‐pRBD yet.ObjectivesThe aim was to investigate cMD as a sensitive measure to identify subtle cortical microstructural changes in PD‐pRBD and its relationship with cortical thickness (CTh).MethodsTwenty‐two PD‐pRBD, 31 PD without probable RBD (PD‐nonpRBD), and 28 healthy controls (HC) were assessed using 3D T1‐weighted and diffusion‐weighted magnetic resonance imaging on a 3‐T scanner and neuropsychological testing. Measures of cortical brain changes were obtained through cMD and CTh. Two‐class group comparisons of a general linear model were performed (P < 0.05). Cohen's d effect size for both approaches was computed.ResultsPD‐pRBD patients showed higher cMD than PD‐nonpRBD patients in the left superior temporal, superior frontal, and precentral gyri, precuneus cortex, as well as in the right middle frontal and postcentral gyri and paracentral lobule (d > 0.8), whereas CTh did not detect significant differences. PD‐pRBD patients also showed increased bilateral posterior cMD in comparison with HCs (d > 0.8). These results partially overlapped with CTh results (0.5 < d < 0.8). PD‐nonpRBD patients showed no differences in cMD when compared with HCs but showed cortical thinning in the left fusiform gyrus and lateral occipital cortex bilaterally (d > 0.5).ConclusionscMD may be more sensitive than CTh displaying significant cortico‐structural differences between PD subgroups, indicating this imaging biomarker's utility in studying early cortical changes in PD. © 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

Ministerio de Economía y Competitividad

Instituto de Salud Carlos III

Ministerio de Ciencia, Innovación y Universidades

Generalitat de Catalunya

H2020 Marie Skłodowska-Curie Actions

'la Caixa' Foundation

Ministerio de Ciencia e Innovación

Publisher

Wiley

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