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Individual parkinsonian motor signs and striatal dopamine transporter deficiency: a study with [I-123]FP-CIT SPECT

INTRODUCTION: Total parkinsonian motor symptom severity correlates with presynaptic striatal dopamine function in patients with Parkinson’s disease. There is a lack of studies that have investigated the associations between parkinsonian motor signs and striatal dopaminergic deficiency in patients wi...

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Autores principales: Mäkinen, Elina, Joutsa, Juho, Jaakkola, Elina, Noponen, Tommi, Johansson, Jarkko, Pitkonen, Miia, Levo, Reeta, Mertsalmi, Tuomas, Scheperjans, Filip, Kaasinen, Valtteri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420881/
https://www.ncbi.nlm.nih.gov/pubmed/30687897
http://dx.doi.org/10.1007/s00415-019-09202-6
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author Mäkinen, Elina
Joutsa, Juho
Jaakkola, Elina
Noponen, Tommi
Johansson, Jarkko
Pitkonen, Miia
Levo, Reeta
Mertsalmi, Tuomas
Scheperjans, Filip
Kaasinen, Valtteri
author_facet Mäkinen, Elina
Joutsa, Juho
Jaakkola, Elina
Noponen, Tommi
Johansson, Jarkko
Pitkonen, Miia
Levo, Reeta
Mertsalmi, Tuomas
Scheperjans, Filip
Kaasinen, Valtteri
author_sort Mäkinen, Elina
collection PubMed
description INTRODUCTION: Total parkinsonian motor symptom severity correlates with presynaptic striatal dopamine function in patients with Parkinson’s disease. There is a lack of studies that have investigated the associations between parkinsonian motor signs and striatal dopaminergic deficiency in patients with parkinsonism of an unknown origin. Identification of specific motor signs associated with the highest likelihood of striatal dopamine deficiency could aid the differential diagnostics of parkinsonian and tremor syndromes. METHODS: In this cross-sectional clinical and imaging study, detailed motor examinations were performed for 221 patients with parkinsonism or tremor of an unknown origin immediately before dopamine transporter (DAT) [I-123]FP-CIT SPECT imaging. Region-of-interest and voxel-based methods were used to investigate striatal DAT deficiency in relation to individual motor signs. RESULTS: Upper extremity rigidity and facial expression were the only motor signs that differentiated patients with normal and abnormal striatal DAT function. The presence of any upper extremity rigidity showed the highest likelihood of DAT deficiency (OR 4.79, 95% CI 1.56–14.75, P = 0.006) followed by reduced facial expression (OR 2.14, 95% CI 1.14–4.00, P = 0.018). In patients with DAT deficits, reduced facial expression was associated with DAT deficiency specifically in the caudate nucleus, and increased upper extremity rigidity was associated with DAT loss in the dorsal putamen (FWE-corrected P < 0.05). CONCLUSIONS: Increased upper extremity muscle tone and hypomimia are independently associated with a higher likelihood of striatal hypodopaminergic imaging finding. This information can be used as a factor when the clinical need of auxiliary investigations, such as DAT SPECT, is considered for patients with parkinsonism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-019-09202-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-64208812019-04-03 Individual parkinsonian motor signs and striatal dopamine transporter deficiency: a study with [I-123]FP-CIT SPECT Mäkinen, Elina Joutsa, Juho Jaakkola, Elina Noponen, Tommi Johansson, Jarkko Pitkonen, Miia Levo, Reeta Mertsalmi, Tuomas Scheperjans, Filip Kaasinen, Valtteri J Neurol Original Communication INTRODUCTION: Total parkinsonian motor symptom severity correlates with presynaptic striatal dopamine function in patients with Parkinson’s disease. There is a lack of studies that have investigated the associations between parkinsonian motor signs and striatal dopaminergic deficiency in patients with parkinsonism of an unknown origin. Identification of specific motor signs associated with the highest likelihood of striatal dopamine deficiency could aid the differential diagnostics of parkinsonian and tremor syndromes. METHODS: In this cross-sectional clinical and imaging study, detailed motor examinations were performed for 221 patients with parkinsonism or tremor of an unknown origin immediately before dopamine transporter (DAT) [I-123]FP-CIT SPECT imaging. Region-of-interest and voxel-based methods were used to investigate striatal DAT deficiency in relation to individual motor signs. RESULTS: Upper extremity rigidity and facial expression were the only motor signs that differentiated patients with normal and abnormal striatal DAT function. The presence of any upper extremity rigidity showed the highest likelihood of DAT deficiency (OR 4.79, 95% CI 1.56–14.75, P = 0.006) followed by reduced facial expression (OR 2.14, 95% CI 1.14–4.00, P = 0.018). In patients with DAT deficits, reduced facial expression was associated with DAT deficiency specifically in the caudate nucleus, and increased upper extremity rigidity was associated with DAT loss in the dorsal putamen (FWE-corrected P < 0.05). CONCLUSIONS: Increased upper extremity muscle tone and hypomimia are independently associated with a higher likelihood of striatal hypodopaminergic imaging finding. This information can be used as a factor when the clinical need of auxiliary investigations, such as DAT SPECT, is considered for patients with parkinsonism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-019-09202-6) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-01-28 2019 /pmc/articles/PMC6420881/ /pubmed/30687897 http://dx.doi.org/10.1007/s00415-019-09202-6 Text en © The Author(s) 2019 OpenAccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Communication
Mäkinen, Elina
Joutsa, Juho
Jaakkola, Elina
Noponen, Tommi
Johansson, Jarkko
Pitkonen, Miia
Levo, Reeta
Mertsalmi, Tuomas
Scheperjans, Filip
Kaasinen, Valtteri
Individual parkinsonian motor signs and striatal dopamine transporter deficiency: a study with [I-123]FP-CIT SPECT
title Individual parkinsonian motor signs and striatal dopamine transporter deficiency: a study with [I-123]FP-CIT SPECT
title_full Individual parkinsonian motor signs and striatal dopamine transporter deficiency: a study with [I-123]FP-CIT SPECT
title_fullStr Individual parkinsonian motor signs and striatal dopamine transporter deficiency: a study with [I-123]FP-CIT SPECT
title_full_unstemmed Individual parkinsonian motor signs and striatal dopamine transporter deficiency: a study with [I-123]FP-CIT SPECT
title_short Individual parkinsonian motor signs and striatal dopamine transporter deficiency: a study with [I-123]FP-CIT SPECT
title_sort individual parkinsonian motor signs and striatal dopamine transporter deficiency: a study with [i-123]fp-cit spect
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420881/
https://www.ncbi.nlm.nih.gov/pubmed/30687897
http://dx.doi.org/10.1007/s00415-019-09202-6
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