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Bipolar Disorder and Parkinson disease: a 123I-FP-CIT SPECT study
INTRODUCTION: Bipolar Disorder (BD) has been suggested to be a risk factor for development of Parkinson Disease. Psychiatric drugs used as standard treatment of BD includes many drugs that are known to induce drug-induced parkinsonism (DIP). OBJECTIVES: Clinical differentiation between PD and DIP is...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10434513/ http://dx.doi.org/10.1192/j.eurpsy.2023.1090 |
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author | D’agostino, G. Cascino, G. Landolfi, A. M. Erro, R. Barone, P. Monteleone, P. |
author_facet | D’agostino, G. Cascino, G. Landolfi, A. M. Erro, R. Barone, P. Monteleone, P. |
author_sort | D’agostino, G. |
collection | PubMed |
description | INTRODUCTION: Bipolar Disorder (BD) has been suggested to be a risk factor for development of Parkinson Disease. Psychiatric drugs used as standard treatment of BD includes many drugs that are known to induce drug-induced parkinsonism (DIP). OBJECTIVES: Clinical differentiation between PD and DIP is a clinical and scientific crucial result. It might be aided by functional neuroimaging of the dopaminergic nigrostriatal pathway. METHODS: Twenty consecutive BD patients with parkinsonism were clinically assessed and underwent (123)I-ioflupane dopamine transporter SPECT. Imaging data of BD patients with pathological nigrostriatal pathway were further compared to a population of de-novo PD patients. RESULTS: Four BD patients had abnormal scans; they had higher putaminal binding ratio and putamen-to-caudate ratios than PD patients, despite similar motor symptom burden. CONCLUSIONS: in our initial results, up to 20% of BD patients with parkinsonism might have an underlying dopaminergic deficit, which is higher than excepted in the general population. This evidences supports that BD represents a risk factor for subsequent development of neurodegenerative parkinsonism. DISCLOSURE OF INTEREST: None Declared |
format | Online Article Text |
id | pubmed-10434513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104345132023-08-18 Bipolar Disorder and Parkinson disease: a 123I-FP-CIT SPECT study D’agostino, G. Cascino, G. Landolfi, A. M. Erro, R. Barone, P. Monteleone, P. Eur Psychiatry Abstract INTRODUCTION: Bipolar Disorder (BD) has been suggested to be a risk factor for development of Parkinson Disease. Psychiatric drugs used as standard treatment of BD includes many drugs that are known to induce drug-induced parkinsonism (DIP). OBJECTIVES: Clinical differentiation between PD and DIP is a clinical and scientific crucial result. It might be aided by functional neuroimaging of the dopaminergic nigrostriatal pathway. METHODS: Twenty consecutive BD patients with parkinsonism were clinically assessed and underwent (123)I-ioflupane dopamine transporter SPECT. Imaging data of BD patients with pathological nigrostriatal pathway were further compared to a population of de-novo PD patients. RESULTS: Four BD patients had abnormal scans; they had higher putaminal binding ratio and putamen-to-caudate ratios than PD patients, despite similar motor symptom burden. CONCLUSIONS: in our initial results, up to 20% of BD patients with parkinsonism might have an underlying dopaminergic deficit, which is higher than excepted in the general population. This evidences supports that BD represents a risk factor for subsequent development of neurodegenerative parkinsonism. DISCLOSURE OF INTEREST: None Declared Cambridge University Press 2023-07-19 /pmc/articles/PMC10434513/ http://dx.doi.org/10.1192/j.eurpsy.2023.1090 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract D’agostino, G. Cascino, G. Landolfi, A. M. Erro, R. Barone, P. Monteleone, P. Bipolar Disorder and Parkinson disease: a 123I-FP-CIT SPECT study |
title | Bipolar Disorder and Parkinson disease: a 123I-FP-CIT SPECT study |
title_full | Bipolar Disorder and Parkinson disease: a 123I-FP-CIT SPECT study |
title_fullStr | Bipolar Disorder and Parkinson disease: a 123I-FP-CIT SPECT study |
title_full_unstemmed | Bipolar Disorder and Parkinson disease: a 123I-FP-CIT SPECT study |
title_short | Bipolar Disorder and Parkinson disease: a 123I-FP-CIT SPECT study |
title_sort | bipolar disorder and parkinson disease: a 123i-fp-cit spect study |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10434513/ http://dx.doi.org/10.1192/j.eurpsy.2023.1090 |
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