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Nigral Iron Deposition Is Associated With Levodopa-Induced Dyskinesia in Parkinson’s Disease
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 valu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019898/ https://www.ncbi.nlm.nih.gov/pubmed/33828454 http://dx.doi.org/10.3389/fnins.2021.647168 |
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author | Song, Tianbin Li, Jiping Mei, Shanshan Jia, Xiaofei Yang, Hongwei Ye, Yongquan Yuan, Jianmin Zhang, Yuqing Lu, Jie |
author_facet | Song, Tianbin Li, Jiping Mei, Shanshan Jia, Xiaofei Yang, Hongwei Ye, Yongquan Yuan, Jianmin Zhang, Yuqing Lu, Jie |
author_sort | Song, Tianbin |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8019898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80198982021-04-06 Nigral Iron Deposition Is Associated With Levodopa-Induced Dyskinesia in Parkinson’s Disease Song, Tianbin Li, Jiping Mei, Shanshan Jia, Xiaofei Yang, Hongwei Ye, Yongquan Yuan, Jianmin Zhang, Yuqing Lu, Jie Front Neurosci Neuroscience 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. Frontiers Media S.A. 2021-03-22 /pmc/articles/PMC8019898/ /pubmed/33828454 http://dx.doi.org/10.3389/fnins.2021.647168 Text en Copyright © 2021 Song, Li, Mei, Jia, Yang, Ye, Yuan, Zhang and Lu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Song, Tianbin Li, Jiping Mei, Shanshan Jia, Xiaofei Yang, Hongwei Ye, Yongquan Yuan, Jianmin Zhang, Yuqing Lu, Jie Nigral Iron Deposition Is Associated With Levodopa-Induced Dyskinesia in Parkinson’s Disease |
title | Nigral Iron Deposition Is Associated With Levodopa-Induced Dyskinesia in Parkinson’s Disease |
title_full | Nigral Iron Deposition Is Associated With Levodopa-Induced Dyskinesia in Parkinson’s Disease |
title_fullStr | Nigral Iron Deposition Is Associated With Levodopa-Induced Dyskinesia in Parkinson’s Disease |
title_full_unstemmed | Nigral Iron Deposition Is Associated With Levodopa-Induced Dyskinesia in Parkinson’s Disease |
title_short | Nigral Iron Deposition Is Associated With Levodopa-Induced Dyskinesia in Parkinson’s Disease |
title_sort | nigral iron deposition is associated with levodopa-induced dyskinesia in parkinson’s disease |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019898/ https://www.ncbi.nlm.nih.gov/pubmed/33828454 http://dx.doi.org/10.3389/fnins.2021.647168 |
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