International Multicenter Analysis of Brain Structure Across Clinical Stages of Parkinson’s Disease
Citation
Max A. Laansma, Joanna K. Bright, Sarah Al-Bachari, Tim J. Anderson, Tyler Ard, Francesca Assogna, Katherine A. Baquero, Henk W. Berendse, Jamie Blair, Fernando Cendes, John C. Dalrymple-Alford, Rob M.A. de Bie, Ines Debove, Michiel F. Dirkx, Jason Druzgal, Hedley C.A. Emsley,Gäetan Garraux, Rachel P. Guimaraes, Boris A. Gutman, Rick C. Helmich, Johannes C. Klein, Clare E. Mackay, Corey T. McMillan, Tracy R. Melzer, Laura M. Parkes, Fabrizio Piras, Toni L. Pitcher, Kathleen L. Poston, Mario Rango, Letícia F. Ribeiro, Cristiane S. Rocha, Christian Rummel, Lucas S.R. Santos, Reinhold Schmidt, Petra Schwingenschuh, Gianfranco Spalletta, Letizia Squarcina, Odile A. van den Heuvel, Chris Vriend, Jiun-Jie Wang, PhD,33,34 Daniel Weintraub, MD, PhD,35 Roland Wiest, PhD,29 Clarissa L. Yasuda, Neda Jahanshad, Paul M. Thompson, Ysbrand D. van der Werf, and The ENIGMA-Parkinson’s Study.International Multicenter Analysis of Brain Structure Across Clinical Stages of Parkinson’s Disease. Movement Disorders 2021.
Abstract
ABSTRACT: 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 sexmatched 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. © 2021 The Authors. Movement
Disorders published by Wiley Periodicals LLC on behalf
of International Parkinson and Movement Disorder
Society