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Grand Total EEG Score Can Differentiate Parkinson's Disease From Parkinson-Related Disorders

Background: Semi-quantitative electroencephalogram (EEG) analysis is easy to perform and has been used to differentiate dementias, as well as idiopathic and vascular Parkinson's disease. Purpose: To study whether a semi-quantitative EEG analysis can aid in distinguishing idiopathic Parkinson�...

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Autores principales: Barcelon, Ela Austria, Mukaino, Takahiko, Yokoyama, Jun, Uehara, Taira, Ogata, Katsuya, Kira, Jun-ichi, Tobimatsu, Shozo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482237/
https://www.ncbi.nlm.nih.gov/pubmed/31057481
http://dx.doi.org/10.3389/fneur.2019.00398
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author Barcelon, Ela Austria
Mukaino, Takahiko
Yokoyama, Jun
Uehara, Taira
Ogata, Katsuya
Kira, Jun-ichi
Tobimatsu, Shozo
author_facet Barcelon, Ela Austria
Mukaino, Takahiko
Yokoyama, Jun
Uehara, Taira
Ogata, Katsuya
Kira, Jun-ichi
Tobimatsu, Shozo
author_sort Barcelon, Ela Austria
collection PubMed
description Background: Semi-quantitative electroencephalogram (EEG) analysis is easy to perform and has been used to differentiate dementias, as well as idiopathic and vascular Parkinson's disease. Purpose: To study whether a semi-quantitative EEG analysis can aid in distinguishing idiopathic Parkinson's disease (IPD) from atypical parkinsonian disorders (APDs), and furthermore, whether it can help to distinguish between APDs. Materials and Methods: A comprehensive retrospective review of charts was performed to include patients with parkinsonian disorders who had at least one EEG recording available. A modified grand total EEG (GTE) score evaluating the posterior background activity, and diffuse and focal slow wave activities was used in further analyses. Results: We analyzed data from 76 patients with a final diagnosis of either IPD, probable corticobasal degeneration (CBD), multiple system atrophy (MSA), or progressive supra-nuclear palsy (PSP). IPD patients had the lowest mean GTE score, followed those with CBD or MSA, while PSP patients scored the highest. However, none of these differences were statistically significant. A GTE score of ≤9 distinguished IPD patients from those with APD (p < 0.01) with a sensitivity of 100% and a specificity of 33.3%. Conclusion: The modified GTE score can distinguish patients with IPD from those with CBD, PSP or MSA at a cut-off score of 9 with excellent sensitivity but poor specificity. However, this score is not able to distinguish a particular form of APD from other forms of the disorder.
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spelling pubmed-64822372019-05-03 Grand Total EEG Score Can Differentiate Parkinson's Disease From Parkinson-Related Disorders Barcelon, Ela Austria Mukaino, Takahiko Yokoyama, Jun Uehara, Taira Ogata, Katsuya Kira, Jun-ichi Tobimatsu, Shozo Front Neurol Neurology Background: Semi-quantitative electroencephalogram (EEG) analysis is easy to perform and has been used to differentiate dementias, as well as idiopathic and vascular Parkinson's disease. Purpose: To study whether a semi-quantitative EEG analysis can aid in distinguishing idiopathic Parkinson's disease (IPD) from atypical parkinsonian disorders (APDs), and furthermore, whether it can help to distinguish between APDs. Materials and Methods: A comprehensive retrospective review of charts was performed to include patients with parkinsonian disorders who had at least one EEG recording available. A modified grand total EEG (GTE) score evaluating the posterior background activity, and diffuse and focal slow wave activities was used in further analyses. Results: We analyzed data from 76 patients with a final diagnosis of either IPD, probable corticobasal degeneration (CBD), multiple system atrophy (MSA), or progressive supra-nuclear palsy (PSP). IPD patients had the lowest mean GTE score, followed those with CBD or MSA, while PSP patients scored the highest. However, none of these differences were statistically significant. A GTE score of ≤9 distinguished IPD patients from those with APD (p < 0.01) with a sensitivity of 100% and a specificity of 33.3%. Conclusion: The modified GTE score can distinguish patients with IPD from those with CBD, PSP or MSA at a cut-off score of 9 with excellent sensitivity but poor specificity. However, this score is not able to distinguish a particular form of APD from other forms of the disorder. Frontiers Media S.A. 2019-04-18 /pmc/articles/PMC6482237/ /pubmed/31057481 http://dx.doi.org/10.3389/fneur.2019.00398 Text en Copyright © 2019 Barcelon, Mukaino, Yokoyama, Uehara, Ogata, Kira and Tobimatsu. 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 Neurology
Barcelon, Ela Austria
Mukaino, Takahiko
Yokoyama, Jun
Uehara, Taira
Ogata, Katsuya
Kira, Jun-ichi
Tobimatsu, Shozo
Grand Total EEG Score Can Differentiate Parkinson's Disease From Parkinson-Related Disorders
title Grand Total EEG Score Can Differentiate Parkinson's Disease From Parkinson-Related Disorders
title_full Grand Total EEG Score Can Differentiate Parkinson's Disease From Parkinson-Related Disorders
title_fullStr Grand Total EEG Score Can Differentiate Parkinson's Disease From Parkinson-Related Disorders
title_full_unstemmed Grand Total EEG Score Can Differentiate Parkinson's Disease From Parkinson-Related Disorders
title_short Grand Total EEG Score Can Differentiate Parkinson's Disease From Parkinson-Related Disorders
title_sort grand total eeg score can differentiate parkinson's disease from parkinson-related disorders
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482237/
https://www.ncbi.nlm.nih.gov/pubmed/31057481
http://dx.doi.org/10.3389/fneur.2019.00398
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