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The potential role of the cardiac MIBG scan in differentiating the drug-induced Parkinsonism from Parkinson’s disease

INTRODUCTION: Considering the difficulties of differentiating Parkinson’s disease (PD) from drug-induced Parkinsonism (DIP) in patients receiving antipsychotics, developing robust diagnostic tools is essential. Herein, we used the metaiodobenzylguanidine (MIBG) scan to assess its diagnostic accuracy...

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Autores principales: Shafie, Mahan, Mayeli, Mahsa, Saeidi, Samira, Mirsepassi, Zahra, Abbasi, Mehrshad, Shafeghat, Melika, Aghamollaii, Vajiheh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802054/
https://www.ncbi.nlm.nih.gov/pubmed/35146407
http://dx.doi.org/10.1016/j.prdoa.2022.100130
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author Shafie, Mahan
Mayeli, Mahsa
Saeidi, Samira
Mirsepassi, Zahra
Abbasi, Mehrshad
Shafeghat, Melika
Aghamollaii, Vajiheh
author_facet Shafie, Mahan
Mayeli, Mahsa
Saeidi, Samira
Mirsepassi, Zahra
Abbasi, Mehrshad
Shafeghat, Melika
Aghamollaii, Vajiheh
author_sort Shafie, Mahan
collection PubMed
description INTRODUCTION: Considering the difficulties of differentiating Parkinson’s disease (PD) from drug-induced Parkinsonism (DIP) in patients receiving antipsychotics, developing robust diagnostic tools is essential. Herein, we used the metaiodobenzylguanidine (MIBG) scan to assess its diagnostic accuracy for this purpose. METHODS: 44 DIP patients and 32 patients with PD as controls were enrolled. All the participants underwent a cardiac (131)I-MIBG scan. Statistical analysis was conducted to determine the significance of the results, and accuracy analyses were conducted to calculate the related sensitivity and specificity of the MIBG scan. RESULTS: The mean age of PD and DIP groups were 62.6 ± 5.9 and 51.5 ± 10.8 years, respectively. The mean duration of drug consumption in the DIP group was 52.2 ± 29.4 days (the mean interval between drug initiation and DIP onset was 28.5 ± 20.5). Symptoms relief occurred 40 ± 24.2 days after drug discontinuation. In the PD group, 15.6% showed negative and 84.4% positive results on the MIBG scan. In the DIP group, 86.4% were negative, and the remaining were positive. The difference in MIBG uptake between the two groups was statistically significant (P-value < 0.001). The sensitivity and specificity of the MIBG scan were 84.4% (CI: 84.0–84.8) and 86.36% (CI: 86.0–86.7) for the diagnosis of PD, respectively. CONCLUSION: Our results indicated more positive MIBG scans in the PD group than the DIP. Also, the MIBG scan’s sensitivity and specificity in differentiating the PD are acceptable. Future works should assess these findings and the role of the MIBG scan in prognosis assessment of DIP and better allocation of the patients to related disciplines.
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spelling pubmed-88020542022-02-09 The potential role of the cardiac MIBG scan in differentiating the drug-induced Parkinsonism from Parkinson’s disease Shafie, Mahan Mayeli, Mahsa Saeidi, Samira Mirsepassi, Zahra Abbasi, Mehrshad Shafeghat, Melika Aghamollaii, Vajiheh Clin Park Relat Disord Original Article INTRODUCTION: Considering the difficulties of differentiating Parkinson’s disease (PD) from drug-induced Parkinsonism (DIP) in patients receiving antipsychotics, developing robust diagnostic tools is essential. Herein, we used the metaiodobenzylguanidine (MIBG) scan to assess its diagnostic accuracy for this purpose. METHODS: 44 DIP patients and 32 patients with PD as controls were enrolled. All the participants underwent a cardiac (131)I-MIBG scan. Statistical analysis was conducted to determine the significance of the results, and accuracy analyses were conducted to calculate the related sensitivity and specificity of the MIBG scan. RESULTS: The mean age of PD and DIP groups were 62.6 ± 5.9 and 51.5 ± 10.8 years, respectively. The mean duration of drug consumption in the DIP group was 52.2 ± 29.4 days (the mean interval between drug initiation and DIP onset was 28.5 ± 20.5). Symptoms relief occurred 40 ± 24.2 days after drug discontinuation. In the PD group, 15.6% showed negative and 84.4% positive results on the MIBG scan. In the DIP group, 86.4% were negative, and the remaining were positive. The difference in MIBG uptake between the two groups was statistically significant (P-value < 0.001). The sensitivity and specificity of the MIBG scan were 84.4% (CI: 84.0–84.8) and 86.36% (CI: 86.0–86.7) for the diagnosis of PD, respectively. CONCLUSION: Our results indicated more positive MIBG scans in the PD group than the DIP. Also, the MIBG scan’s sensitivity and specificity in differentiating the PD are acceptable. Future works should assess these findings and the role of the MIBG scan in prognosis assessment of DIP and better allocation of the patients to related disciplines. Elsevier 2022-01-07 /pmc/articles/PMC8802054/ /pubmed/35146407 http://dx.doi.org/10.1016/j.prdoa.2022.100130 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Shafie, Mahan
Mayeli, Mahsa
Saeidi, Samira
Mirsepassi, Zahra
Abbasi, Mehrshad
Shafeghat, Melika
Aghamollaii, Vajiheh
The potential role of the cardiac MIBG scan in differentiating the drug-induced Parkinsonism from Parkinson’s disease
title The potential role of the cardiac MIBG scan in differentiating the drug-induced Parkinsonism from Parkinson’s disease
title_full The potential role of the cardiac MIBG scan in differentiating the drug-induced Parkinsonism from Parkinson’s disease
title_fullStr The potential role of the cardiac MIBG scan in differentiating the drug-induced Parkinsonism from Parkinson’s disease
title_full_unstemmed The potential role of the cardiac MIBG scan in differentiating the drug-induced Parkinsonism from Parkinson’s disease
title_short The potential role of the cardiac MIBG scan in differentiating the drug-induced Parkinsonism from Parkinson’s disease
title_sort potential role of the cardiac mibg scan in differentiating the drug-induced parkinsonism from parkinson’s disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802054/
https://www.ncbi.nlm.nih.gov/pubmed/35146407
http://dx.doi.org/10.1016/j.prdoa.2022.100130
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