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Loss of substantia nigra hyperintensity on 7 Tesla MRI of Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy

Authors
Kim, Jong-MinJeong, Hye-JinBae, Yun JungPark, Sung-YeonKim, EunheeKang, Seo YoungOh, Eung SeokKim, Kyeong JoonJeon, BeomseokKim, Sang EunCho, Zang-HeeKim, Young-Bo
Issue Date
May-2016
Publisher
ELSEVIER SCI LTD
Keywords
Magnetic resonance imaging; Parkinson' s disease; Multiple system atrophy; Progressive supranuclear palsy
Citation
PARKINSONISM & RELATED DISORDERS, v.26, pp.47 - 54
Journal Title
PARKINSONISM & RELATED DISORDERS
Volume
26
Start Page
47
End Page
54
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/8307
DOI
10.1016/j.parkreldis.2016.01.023
ISSN
1353-8020
Abstract
Background: Seven Tesla (7T) MRI can visualize anatomical alterations occurring in a hyperintense structure of the substantia nigra in Parkinson's disease (PD). Objective: We investigated whether 7T MRI can detect the loss of substantia nigra hyperintensity in patients with PD, multiple system atrophy (MSA), and progressive supranuclear palsy (PSP). Methods: Using 7T MRI, we evaluated 26 healthy subjects, 30 patients with PD, 7 patients with MSA, and 3 patients with PSP. Two blinded readers independently assessed the images. We carried out a comparative analysis of five patients with hemiparkinsonism via I-123-2 beta-carbomethoxy-3 beta-(4-iodophenyl)-N-(3-fluoropropyl)-nortropane (I-123-FP-CIT) SPECT. Results: 7T MRI revealed a definitive shape of nigral hyperintensity in healthy subjects, nearly identical to neuropathological characterization of nigrosome 1, and enabled instantaneous determination of its presence or absence in all subjects. Nigral hyperintensity was lost in all patients with PD, MSA with predominant parkinsonism, and PSP. One of five patients with MSA with predominant cerebellar ataxia showed an intact nigral hyperintensity. The side effects were mild and tolerable, and imaging was successful in patients with dyskinesia. Motion artifact incidence was higher in elderly subjects. In hemiparkinsonism cases, we observed partial loss of nigral hyperintensity on the side of less reduced I-123-FP-CIT binding, suggesting an ongoing iron deposition on the unaffected side in hemiparkinsonism. Conclusions: The present findings suggest that 7T MRI represents an excellent tool for evaluating nigral hyperintensity in PD, MSA, and PSP, with tolerable side effects and limited motion artifacts. Thus, imaging of parkinsonism may benefit from using 7T MRI. (C) 2016 Elsevier Ltd. All rights reserved.
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