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Brain regional iron contents in progressive supranuclear palsy




TekijätSeung Ha Lee, Chul Hyoung Lyoo, Sung Jun Ahn, Juha O. Rinne, Myung Sik Lee

KustantajaElsevier Ltd

Julkaisuvuosi2017

JournalParkinsonism and Related Disorders

Tietokannassa oleva lehden nimiParkinsonism and Related Disorders

Vuosikerta45

Aloitussivu28

Lopetussivu32

Sivujen määrä5

ISSN1353-8020

eISSN1873-5126

DOIhttps://doi.org/10.1016/j.parkreldis.2017.09.020


Tiivistelmä
Introduction

To determine motor-related brain regions in which iron contents correlate with the degree of motor deficits of progressive supranuclear palsy (PSP).

Methods

Twenty-four patients with probable PSP and 20 controls were included. Using a 3.0T magnetic resonance imaging scanner, R2* values were measured in the putamen, globus pallidus (GP), substantia nigra (SN), subthalamic nucleus, and dentate nucleus. After adjustment for disease duration and age at examination, correlations between regional brain R2* values and Unified Parkinson Disease Rating Scale (UPDRS) total motor scores or subscores for bradykinesia, rigidity, tremor, or axial motor deficits were investigated.

Results

Compared to controls, patients with PSP had significantly higher R2* values in all of the five brain regions. UPDRS
total motor scores and subscores for bradykinesia and axial motor
deficits did not correlate with R2* values of the five brain regions.
However, UPDRS subscores for unilateral rigidity were correlated with
R2* values of the contralateral putamen and GP. In addition, unilateral
UPDRS subscores for tremor were associated with R2* values of the
ipsilateral dentate nucleus, contralateral putamen, GP, and SN.

Conclusion

In PSP, excessive iron accumulation occurs in motor-related subcortical regions. Iron-related PSP pathologies in the lenticular nucleus
are associated with rigidity severity, while those in the
nigro-striato-pallidal unit and dentate nucleus are associated with
tremor severity. Bradykinesia and axial motor deficits of PSP seem to be
associated with widespread pathologies in the cerebrum, brainstem, cerebellum, as well as the basal ganglia.



Last updated on 2024-26-11 at 23:41