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A Retrospective Imaging Evaluation of Presynaptic Dopaminergic Degeneration in Multiple System Atrophy with Levodopa Induced Dyskinesia

BACKGROUND: Multiple system atrophy (MSA) may develop levodopa-induced dyskinesia, which is dystonic and predominant in the orofacial region. We aimed to characterize the patterns of presynaptic dopaminergic degeneration in patients with MSA and dyskinesia using (123)I-N-x-fluoropropyl-2b-carbo-meth...

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Autores principales: Ueno, Shin-ichi, Oyama, Genko, Kanai, Kazuaki, Hatano, Taku, Shimo, Yasushi, Hattori, Nobutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ubiquity Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394229/
https://www.ncbi.nlm.nih.gov/pubmed/32775020
http://dx.doi.org/10.5334/tohm.58
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author Ueno, Shin-ichi
Oyama, Genko
Kanai, Kazuaki
Hatano, Taku
Shimo, Yasushi
Hattori, Nobutaka
author_facet Ueno, Shin-ichi
Oyama, Genko
Kanai, Kazuaki
Hatano, Taku
Shimo, Yasushi
Hattori, Nobutaka
author_sort Ueno, Shin-ichi
collection PubMed
description BACKGROUND: Multiple system atrophy (MSA) may develop levodopa-induced dyskinesia, which is dystonic and predominant in the orofacial region. We aimed to characterize the patterns of presynaptic dopaminergic degeneration in patients with MSA and dyskinesia using (123)I-N-x-fluoropropyl-2b-carbo-methoxy-3b-(4-iodophenyl) nortropan single-photon emission computed tomography ((123)I-FP-CIT SPECT). METHODS: A single center cross-sectional retrospective study was conducted using consecutive chart review of patients with probable MSA who underwent (123)I-FP-CIT SPECT. The degeneration patterns were compared between the groups with and without dyskinesia via visual assessment of (123)I-FP-CIT SPECT images. RESULTS: Twenty-five patients with probable MSA who had undergone dopamine transporter imaging were identified (age [mean ± standard error], 62.5 ± 1.7 years; disease duration, 48.8 ± 7.0 months). Four of them presented dyskinesia and 21 of patients did not. Twenty-five patients with MSA were visually classified into five grades: one Grade 1 (normal), two Grade 2 (eagle wing), three Grade 3 (mixed), nine Grade 4 (egg shape), and ten Grade 5 (burst striatum). All patients with MSA and dyskinesia were classified into Grade 5. Visual grading significantly correlated with disease duration and levodopa responsiveness. CONCLUSIONS: Severe presynaptic dopaminergic dysfunction in (123)I-FP-CIT SPECT images, higher doses of dopaminergic medication, and longer disease durations were associated with occurrence of levodopa-induced dyskinesia, even in MSA.
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spelling pubmed-73942292020-08-07 A Retrospective Imaging Evaluation of Presynaptic Dopaminergic Degeneration in Multiple System Atrophy with Levodopa Induced Dyskinesia Ueno, Shin-ichi Oyama, Genko Kanai, Kazuaki Hatano, Taku Shimo, Yasushi Hattori, Nobutaka Tremor Other Hyperkinet Mov (N Y) Article BACKGROUND: Multiple system atrophy (MSA) may develop levodopa-induced dyskinesia, which is dystonic and predominant in the orofacial region. We aimed to characterize the patterns of presynaptic dopaminergic degeneration in patients with MSA and dyskinesia using (123)I-N-x-fluoropropyl-2b-carbo-methoxy-3b-(4-iodophenyl) nortropan single-photon emission computed tomography ((123)I-FP-CIT SPECT). METHODS: A single center cross-sectional retrospective study was conducted using consecutive chart review of patients with probable MSA who underwent (123)I-FP-CIT SPECT. The degeneration patterns were compared between the groups with and without dyskinesia via visual assessment of (123)I-FP-CIT SPECT images. RESULTS: Twenty-five patients with probable MSA who had undergone dopamine transporter imaging were identified (age [mean ± standard error], 62.5 ± 1.7 years; disease duration, 48.8 ± 7.0 months). Four of them presented dyskinesia and 21 of patients did not. Twenty-five patients with MSA were visually classified into five grades: one Grade 1 (normal), two Grade 2 (eagle wing), three Grade 3 (mixed), nine Grade 4 (egg shape), and ten Grade 5 (burst striatum). All patients with MSA and dyskinesia were classified into Grade 5. Visual grading significantly correlated with disease duration and levodopa responsiveness. CONCLUSIONS: Severe presynaptic dopaminergic dysfunction in (123)I-FP-CIT SPECT images, higher doses of dopaminergic medication, and longer disease durations were associated with occurrence of levodopa-induced dyskinesia, even in MSA. Ubiquity Press 2020-06-15 /pmc/articles/PMC7394229/ /pubmed/32775020 http://dx.doi.org/10.5334/tohm.58 Text en Copyright: © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC-BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ueno, Shin-ichi
Oyama, Genko
Kanai, Kazuaki
Hatano, Taku
Shimo, Yasushi
Hattori, Nobutaka
A Retrospective Imaging Evaluation of Presynaptic Dopaminergic Degeneration in Multiple System Atrophy with Levodopa Induced Dyskinesia
title A Retrospective Imaging Evaluation of Presynaptic Dopaminergic Degeneration in Multiple System Atrophy with Levodopa Induced Dyskinesia
title_full A Retrospective Imaging Evaluation of Presynaptic Dopaminergic Degeneration in Multiple System Atrophy with Levodopa Induced Dyskinesia
title_fullStr A Retrospective Imaging Evaluation of Presynaptic Dopaminergic Degeneration in Multiple System Atrophy with Levodopa Induced Dyskinesia
title_full_unstemmed A Retrospective Imaging Evaluation of Presynaptic Dopaminergic Degeneration in Multiple System Atrophy with Levodopa Induced Dyskinesia
title_short A Retrospective Imaging Evaluation of Presynaptic Dopaminergic Degeneration in Multiple System Atrophy with Levodopa Induced Dyskinesia
title_sort retrospective imaging evaluation of presynaptic dopaminergic degeneration in multiple system atrophy with levodopa induced dyskinesia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394229/
https://www.ncbi.nlm.nih.gov/pubmed/32775020
http://dx.doi.org/10.5334/tohm.58
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