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  3. International Multicenter Analysis of Brain Structure Across Clinical Stages of Parkinson's Disease.
 

International Multicenter Analysis of Brain Structure Across Clinical Stages of Parkinson's Disease.

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BORIS DOI
10.48350/159375
Date of Publication
November 2021
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Universitätsinstitut ...

Contributor
Laansma, Max A
Bright, Joanna K
Al-Bachari, Sarah
Anderson, Tim J
Ard, Tyler
Assogna, Francesca
Baquero, Katherine A
Berendse, Henk W
Blair, Jamie
Cendes, Fernando
Dalrymple-Alford, John C
de Bie, Rob M A
Debove, Ines
Universitätsklinik für Neurologie
Dirkx, Michiel F
Druzgal, Jason
Emsley, Hedley C A
Garraux, Gäetan
Guimarães, Rachel P
Gutman, Boris A
Helmich, Rick C
Klein, Johannes C
Mackay, Clare E
McMillan, Corey T
Melzer, Tracy R
Parkes, Laura M
Piras, Fabrizio
Pitcher, Toni L
Poston, Kathleen L
Rango, Mario
Ribeiro, Letícia F
Rocha, Cristiane S
Rummel, Christian
Santos, Lucas S R
Schmidt, Reinhold
Schwingenschuh, Petra
Spalletta, Gianfranco
Squarcina, Letizia
van den Heuvel, Odile A
Vriend, Chris
Wang, Jiun-Jie
Weintraub, Daniel
Wiest, Roland Gerhard Rudi
Universitätsinstitut für Diagnostische und Interventionelle Neuroradiologie
Yasuda, Clarissa L
Jahanshad, Neda
Thompson, Paul M
van der Werf, Ysbrand D
Subject(s)

600 - Technology::610...

Series
Movement disorders
ISSN or ISBN (if monograph)
0885-3185
Publisher
Wiley-Blackwell
Language
English
Publisher DOI
10.1002/mds.28706
PubMed ID
34288137
Uncontrolled Keywords

ENIGMA MRI Parkinson'...

Description
BACKGROUND

Brain structure abnormalities throughout the course of Parkinson's disease have yet to be fully elucidated.

OBJECTIVE

Using a multicenter approach and harmonized analysis methods, we aimed to shed light on Parkinson's disease stage-specific profiles of pathology, as suggested by in vivo neuroimaging.

METHODS

Individual brain MRI and clinical data from 2357 Parkinson's disease patients and 1182 healthy controls were collected from 19 sources. We analyzed regional cortical thickness, cortical surface area, and subcortical volume using mixed-effects models. Patients grouped according to Hoehn and Yahr stage were compared with age- and sex-matched controls. Within the patient sample, we investigated associations with Montreal Cognitive Assessment score.

RESULTS

Overall, patients showed a thinner cortex in 38 of 68 regions compared with controls (dmax  = -0.20, dmin  = -0.09). The bilateral putamen (dleft  = -0.14, dright  = -0.14) and left amygdala (d = -0.13) were smaller in patients, whereas the left thalamus was larger (d = 0.13). Analysis of staging demonstrated an initial presentation of thinner occipital, parietal, and temporal cortices, extending toward rostrally located cortical regions with increased disease severity. From stage 2 and onward, the bilateral putamen and amygdala were consistently smaller with larger differences denoting each increment. Poorer cognition was associated with widespread cortical thinning and lower volumes of core limbic structures.

CONCLUSIONS

Our findings offer robust and novel imaging signatures that are generally incremental across but in certain regions specific to disease stages. Our findings highlight the importance of adequately powered multicenter collaborations.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/43744
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