Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783610290832670720 |
---|---|
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). |
format | Online Article Text |
id | pubmed-7667335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zhaoping clinicalfeaturesmriand18ffdgpetindifferentialdiagnosisofparkinsondiseasefrommultiplesystematrophy AT zhangbenshu clinicalfeaturesmriand18ffdgpetindifferentialdiagnosisofparkinsondiseasefrommultiplesystematrophy AT gaoshuo clinicalfeaturesmriand18ffdgpetindifferentialdiagnosisofparkinsondiseasefrommultiplesystematrophy AT lixin clinicalfeaturesmriand18ffdgpetindifferentialdiagnosisofparkinsondiseasefrommultiplesystematrophy |