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Nigrosome 1 visibility and its association with nigrostriatal dopaminergic loss in Parkinson's disease.
Kim, Han-Kyeol; Kim, Taewon; Baek, Min Seok; Kim, Eung Yeop; Sung, Young Hee; Lee, Jae Hoon; Ryu, Young Hoon; Ahn, Sung Jun; Yoo, Han Soo; Lyoo, Chul Hyoung.
Afiliação
  • Kim HK; Department of Neurology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
  • Kim T; Department of Neurology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
  • Baek MS; Department of Neurology, Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju, South Korea.
  • Kim EY; Department of Radiology, Samsung Medical Center, Sungkyunkwan University College of Medicine, Seoul, South Korea.
  • Sung YH; Department of Neurology, Gachon University Gil Medical Center, Incheon, South Korea.
  • Lee JH; Department of Radiology, Gangnam Severance Hospital, College of Medicine, Yonsei University, Seoul, South Korea.
  • Ryu YH; Department of Radiology, Gangnam Severance Hospital, College of Medicine, Yonsei University, Seoul, South Korea.
  • Ahn SJ; Department of Nuclear Medicine, Gangnam Severance Hospital, College of Medicine, Yonsei University, Seoul, South Korea.
  • Yoo HS; Department of Neurology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
  • Lyoo CH; Department of Neurology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Eur J Neurol ; 30(6): 1639-1647, 2023 06.
Article em En | MEDLINE | ID: mdl-36915220
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Coréia do Sul

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Coréia do Sul