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Clinical features, MRI, and 18F‐FDG‐PET in differential diagnosis of Parkinson disease from multiple system atrophy

OBJECTIVE: This study aimed to differentiate the variations in the clinical characteristics, MRI irregularity, and glucose metabolism on (18)F‐FDG‐PET for the differential diagnosis of Parkinson's Disease (PD), MSA with predominant Parkinsonism (MSA‐P), and MSA with predominant cerebellar featu...

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Autores principales: Zhao, Ping, Zhang, Benshu, Gao, Shuo, Li, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667335/
https://www.ncbi.nlm.nih.gov/pubmed/32940411
http://dx.doi.org/10.1002/brb3.1827
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author Zhao, Ping
Zhang, Benshu
Gao, Shuo
Li, Xin
author_facet Zhao, Ping
Zhang, Benshu
Gao, Shuo
Li, Xin
author_sort Zhao, Ping
collection PubMed
description OBJECTIVE: This study aimed to differentiate the variations in the clinical characteristics, MRI irregularity, and glucose metabolism on (18)F‐FDG‐PET for the differential diagnosis of Parkinson's Disease (PD), MSA with predominant Parkinsonism (MSA‐P), and MSA with predominant cerebellar features (MSA‐C). METHODS: Thirty PD patients, 22 MSA‐P patients, and 28 MSA‐C patients received an MRI and 20 PD patients, 11 MSA‐P patients, and 13 MSA‐C patients received (18)F‐FDG‐PET. RESULTS: Firstly, we found that the clinical data presented a tremor at rest, bradykinesia, and postural instability that was predominated in PD (100%), MSA‐P (86.4%), and MSA‐C (53.6%) patients, respectively. Then, we used MRI analyses and found that putamina atrophy and hyperintensive rim (T(2)WI) were characteristic features in MSA‐P and cerebellar atrophy, the “hot cross bun” sign and signal rise in the middle cerebellar peduncle were more obvious in MSA‐C. To further explore the distinctions among the 3 diseases, we also used 18F‐FDG‐PET technology for our examination and found a decrease in glucose metabolism in the parietal area for Parkinson's Disease (PD), in the bilateral putamen for MSA‐P, and in the bilateral cerebellum for MSA‐C. CONCLUSION: This study identified the distinctive features of the clinic symptoms, MRI irregularity, and glucose metabolism on (18)F‐FDG‐PET, which provided a new basis for the differential diagnosis of Parkinson's Disease (PD), MSA with predominant Parkinsonism (MSA‐P), and MSA with predominant cerebellar features (MSA‐C).
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spelling pubmed-76673352020-11-20 Clinical features, MRI, and 18F‐FDG‐PET in differential diagnosis of Parkinson disease from multiple system atrophy Zhao, Ping Zhang, Benshu Gao, Shuo Li, Xin Brain Behav Original Research OBJECTIVE: This study aimed to differentiate the variations in the clinical characteristics, MRI irregularity, and glucose metabolism on (18)F‐FDG‐PET for the differential diagnosis of Parkinson's Disease (PD), MSA with predominant Parkinsonism (MSA‐P), and MSA with predominant cerebellar features (MSA‐C). METHODS: Thirty PD patients, 22 MSA‐P patients, and 28 MSA‐C patients received an MRI and 20 PD patients, 11 MSA‐P patients, and 13 MSA‐C patients received (18)F‐FDG‐PET. RESULTS: Firstly, we found that the clinical data presented a tremor at rest, bradykinesia, and postural instability that was predominated in PD (100%), MSA‐P (86.4%), and MSA‐C (53.6%) patients, respectively. Then, we used MRI analyses and found that putamina atrophy and hyperintensive rim (T(2)WI) were characteristic features in MSA‐P and cerebellar atrophy, the “hot cross bun” sign and signal rise in the middle cerebellar peduncle were more obvious in MSA‐C. To further explore the distinctions among the 3 diseases, we also used 18F‐FDG‐PET technology for our examination and found a decrease in glucose metabolism in the parietal area for Parkinson's Disease (PD), in the bilateral putamen for MSA‐P, and in the bilateral cerebellum for MSA‐C. CONCLUSION: This study identified the distinctive features of the clinic symptoms, MRI irregularity, and glucose metabolism on (18)F‐FDG‐PET, which provided a new basis for the differential diagnosis of Parkinson's Disease (PD), MSA with predominant Parkinsonism (MSA‐P), and MSA with predominant cerebellar features (MSA‐C). John Wiley and Sons Inc. 2020-09-17 /pmc/articles/PMC7667335/ /pubmed/32940411 http://dx.doi.org/10.1002/brb3.1827 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Zhao, Ping
Zhang, Benshu
Gao, Shuo
Li, Xin
Clinical features, MRI, and 18F‐FDG‐PET in differential diagnosis of Parkinson disease from multiple system atrophy
title Clinical features, MRI, and 18F‐FDG‐PET in differential diagnosis of Parkinson disease from multiple system atrophy
title_full Clinical features, MRI, and 18F‐FDG‐PET in differential diagnosis of Parkinson disease from multiple system atrophy
title_fullStr Clinical features, MRI, and 18F‐FDG‐PET in differential diagnosis of Parkinson disease from multiple system atrophy
title_full_unstemmed Clinical features, MRI, and 18F‐FDG‐PET in differential diagnosis of Parkinson disease from multiple system atrophy
title_short Clinical features, MRI, and 18F‐FDG‐PET in differential diagnosis of Parkinson disease from multiple system atrophy
title_sort clinical features, mri, and 18f‐fdg‐pet in differential diagnosis of parkinson disease from multiple system atrophy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667335/
https://www.ncbi.nlm.nih.gov/pubmed/32940411
http://dx.doi.org/10.1002/brb3.1827
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