4.6 Article

Nigral Iron Deposition Is Associated With Levodopa-Induced Dyskinesia in Parkinson's Disease

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FRONTIERS IN NEUROSCIENCE
卷 15, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fnins.2021.647168

关键词

Parkinsion’ s disease; dyskinesia; levodopa; quantitative susceptibility mapping; substantia nigra

资金

  1. Beijing Municipal Administration of Hospitals' Ascent Plan [DFL20180802]
  2. Wu Jieping Medical Foundation [320.6750.19089-78]

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This study found higher iron deposition in the substantia nigra of PD patients with LID compared to those without LID. The QSM value of the SN may be a potential early diagnostic neuroimaging biomarker for LID.
Objective To investigate iron deposition in the substantia nigra (SN) of Parkinson's disease (PD) patients associated with levodopa-induced dyskinesia (LID). Methods Seventeen PD patients with LID, 17 PD patients without LID, and 16 healthy controls were recruited for this study. The mean QSM values of the whole, left, and right SN were compared among the three groups. A multivariate logistic regression model was constructed to determine the factors associated with increased risk of LID. The receiver operating characteristic curve of the QSM value of SN in discriminating PD with and without LID was evaluated. Results The mean QSM values of the whole and right SN in the PD with LID were higher than those in the PD without LID (*P = 0.03, *P = 0.03). Multivariate logistic regression analysis revealed that the QSM value of whole, left, or right SN was a predictor of the development of LID (*P = 0.03, *P = 0.04, and *P = 0.04). The predictive accuracy of LID in adding the QSM value of the whole, left, and right SN to LID-related clinical risk factors was 70.6, 64.7, and 67.6%, respectively. The QSM cutoff values between PD with and without LID of the whole, left, and right SN were 148.3, 165.4, and 152.7 ppb, respectively. Conclusion This study provides the evidence of higher iron deposition in the SN of PD patients with LID than those without LID, suggesting that the QSM value of the SN may be a potential early diagnostic neuroimaging biomarker for LID.

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