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Nigrosome 1 visibility and its association with nigrostriatal dopaminergic loss in Parkinson's disease

Authors
 Han-Kyeol Kim  ;  Taewon Kim  ;  Min Seok Baek  ;  Eung Yeop Kim  ;  Young Hee Sung  ;  Jae Hoon Lee  ;  Young Hoon Ryu  ;  Sung Jun Ahn  ;  Han Soo Yoo  ;  Chul Hyoung Lyoo 
Citation
 EUROPEAN JOURNAL OF NEUROLOGY, Vol.30(6) : 1639-1647, 2023-06 
Journal Title
EUROPEAN JOURNAL OF NEUROLOGY
ISSN
 1351-5101 
Issue Date
2023-06
MeSH
Corpus Striatum / diagnostic imaging ; Corpus Striatum / metabolism ; Dopamine / metabolism ; Dopamine Plasma Membrane Transport Proteins / metabolism ; Humans ; Parkinson Disease* / complications ; Positron-Emission Tomography / methods ; Substantia Nigra / diagnostic imaging ; Substantia Nigra / metabolism ; Tomography, Emission-Computed, Single-Photon / methods ; Tropanes / metabolism
Keywords
Parkinson's disease ; SMwI ; dopamine transporter ; nigrosome 1 ; nigrostriatal degeneration ; visual assessment
Abstract
Background: Nigrosome 1 (NG1), a small cluster of dopaminergic cells in the substantia nigra and visible in the susceptibility map-weighted magnetic resonance image (SMwI), is severely affected in Parkinson's disease (PD). However, the degree of nigrostriatal degeneration according to the visibility of NG1 has not yet been well elucidated.

Methods: We consecutively recruited 138 PD and 78 non-neurodegenerative disease (non-ND) patients, who underwent both 18 F-FP-CIT positron emission tomography (PET) and SMwI. Three neurologists and one radiologist evaluated the visibility of NG1 in SMwI. The participants were thereby grouped into visible, intermediate, and non-visible groups. Nigrostriatal dopaminergic input was calculated using the specific binding ratio (SBR) of the 18 F-FP-CIT PET. We determined the threshold of regional SBR for discriminating NG1 visibility and the probability for NG1 visibility according to regional SBR.

Results: Visual rating of NG1 showed excellent interobserver agreements as well as high sensitivity and specificity to differentiate the PD group from the non-ND group. NG1 was visible in seven patients (5.1%) in the PD group, who had relatively short disease duration or less severe loss of striatal dopamine. The threshold of putaminal SBR reduction on the more affected side for the disappearance of NG1 was 45.5%, and the probability for NG1 visibility dropped to 50% after the reduction of putaminal SBR to 41% from the normal mean.

Conclusions: Almost half loss of nigrostriatal dopaminergic input is required to dissipate the hyperintensity of NG1 on SMwI, suggesting its utility in diagnosing PD only after the onset of the motor symptoms.
Full Text
https://onlinelibrary.wiley.com/doi/10.1111/ene.15781
DOI
10.1111/ene.15781
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Nuclear Medicine (핵의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers
Yonsei Authors
Kim, Han kyeol(김한결) ORCID logo https://orcid.org/0000-0002-7650-6708
Lyoo, Chul Hyoung(류철형) ORCID logo https://orcid.org/0000-0003-2231-672X
Ahn, Sung Jun(안성준) ORCID logo https://orcid.org/0000-0003-0075-2432
Ryu, Young Hoon(유영훈) ORCID logo https://orcid.org/0000-0002-9000-5563
Yoo, Han Soo(유한수) ORCID logo https://orcid.org/0000-0001-7846-6271
Lee, Jae Hoon(이재훈) ORCID logo https://orcid.org/0000-0002-9898-9886
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/195324
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