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Rapid eye movement sleep behaviour disorder and striatal dopamine depletion in patients with Parkinson's disease

Authors
Chung, Su JinLee, Yang-hyunLee, Jae-jungLee, Phil-hyuSohn, Youngho
Issue Date
Oct-2017
Publisher
WILEY-BLACKWELL
Keywords
dopamine; Parkinson' s disease; positron emission tomography; REM sleep behaviour disorder; striatum
Citation
EUROPEAN JOURNAL OF NEUROLOGY, v.24, no.10, pp.1314 - 1319
Indexed
SCIE
SCOPUS
Journal Title
EUROPEAN JOURNAL OF NEUROLOGY
Volume
24
Number
10
Start Page
1314
End Page
1319
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/151429
DOI
10.1111/ene.13388
ISSN
1351-5101
Abstract
Background and purpose: Rapid eye movement sleep behaviour disorder (RBD) is related to striatal dopamine depletion. This study was performed to confirm whether clinically probable RBD (cpRBD) in patients with Parkinson's disease (PD) is associated with a specific pattern of striatal dopamine depletion. Methods : A prospective survey was conducted using the RBD Screening Questionnaire (RBDSQ) in 122 patients with PD who had undergone dopamine transporter (DAT) positron emission tomography scan. Results: Patients with cpRBD (RBDSQ ≥ 7) exhibited greater motor deficits, predominantly in the less-affected side and axial symptoms, and were prescribed higher levodopa-equivalent doses at follow-up than those without cpRBD (RBDSQ ≤ 4), despite their similar disease and treatment durations. Compared to patients without cpRBD, those with cpRBD showed lower DAT activities in the putamen, particularly in the less-affected side in all putaminal subregions, and a tendency to be lower in the ventral striatum. In addition, greater motor deficits in patients with cpRBD than in those without cpRBD remained significant after controlling for DAT binding in the putamen and other confounding variables. Conclusions : These results demonstrated that the presence of RBD in patients with PD is associated with different patterns of both motor deficit distribution and striatal DAT depletion, suggesting that the presence of RBD represents a distinct PD subtype with a malignant motor parkinsonism.
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