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Multimodal Imaging of Substantia Nigra in Parkinson's Disease with Levodopa-Induced Dyskinesia.
Su, Dongning; Gan, Yawen; Zhang, Zhe; Cui, Yusha; Zhang, Zhijin; Liu, Zhu; Wang, Zhan; Zhou, Junhong; Sossi, Vesna; Stoessl, A Jon; Wu, Tao; Jing, Jing; Feng, Tao.
Afiliação
  • Su D; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Gan Y; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Zhang Z; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Cui Y; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Zhang Z; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Liu Z; Tiantan Neuroimaging Center of Excellence, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Wang Z; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Zhou J; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Sossi V; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Stoessl AJ; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Wu T; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Jing J; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Feng T; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Mov Disord ; 38(4): 616-625, 2023 04.
Article em En | MEDLINE | ID: mdl-36799459
BACKGROUND: Degeneration of the substantia nigra (SN) may contribute to levodopa-induced dyskinesia (LID) in Parkinson's disease (PD), but the exact characteristics of SN in LID remain unclear. OBJECTIVE: To further understand the pathogenesis of patients with PD with LID (PD-LID), we explored the structural and functional characteristics of SN in PD-LID using multimodal magnetic resonance imaging (MRI). METHODS: Twenty-nine patients with PD-LID, 37 patients with PD without LID (PD-nLID), and 28 healthy control subjects underwent T1-weighted MRI, quantitative susceptibility mapping, neuromelanin-sensitive MRI, multishell diffusion MRI, and resting-state functional MRI. Different measures characterizing the SN were obtained using a region of interest-based approach. RESULTS: Compared with patients with PD-nLID and healthy control subjects, the quantitative susceptibility mapping values of SN pars compacta (SNpc) were significantly higher (P = 0.049 and P = 0.00002), and the neuromelanin contrast-to-noise ratio values in SNpc were significantly lower (P = 0.012 and P = 0.000002) in PD-LID. The intracellular volume fraction of the posterior SN in PD-LID was significantly higher compared with PD-nLID (P = 0.037). Resting-state fMRI indicated that PD-LID in the medication off state showed higher functional connectivity between the SNpc and putamen compared with PD-nLID (P = 0.031), and the functional connectivity changes in PD-LID were positively correlated with Unified Dyskinesia Rating Scale total scores (R = 0.427, P = 0.042). CONCLUSIONS: Our multimodal imaging findings highlight greater neurodegeneration in SN and the altered nigrostriatal connectivity in PD-LID. These characteristics provide a new perspective into the role of SN in the pathophysiological mechanisms underlying PD-LID. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Discinesias Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Discinesias Idioma: En Ano de publicação: 2023 Tipo de documento: Article