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TRODAT SPECT in patients with idiopathic REM sleep behaviour disorder

to determine the value of dopamine transporter (DAT) neuroimaging radiotracer in a group of idiopathic rapid eye movement sleep behavior disorder (iRBD) patients regarding the development of a synucleinopathy. Methods: 6 retrospectively selected patients with clinical and polysomnographic diagnosis...

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Autor principal: Rizzo, Geraldo Nunes Vieira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brazilian Association of Sleep and Latin American Federation of Sleep 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056068/
https://www.ncbi.nlm.nih.gov/pubmed/30083292
http://dx.doi.org/10.5935/1984-0063.20180014
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author Rizzo, Geraldo Nunes Vieira
author_facet Rizzo, Geraldo Nunes Vieira
author_sort Rizzo, Geraldo Nunes Vieira
collection PubMed
description to determine the value of dopamine transporter (DAT) neuroimaging radiotracer in a group of idiopathic rapid eye movement sleep behavior disorder (iRBD) patients regarding the development of a synucleinopathy. Methods: 6 retrospectively selected patients with clinical and polysomnographic diagnosis of iRBD, on treatment or not, were submitted to a single-photon emission computerized tomography (SPECT) with TRODAT. Results: Five from six patients have an abnormal test showing reduction in DAT density measured by the linkage potential on SPECT. Conclusions: TRODAT crosses the blood brain barrier, has a high affinity for DAT and is capture by SPECT. The decreased uptake of DAT tracers means a reduction in dopaminergic activity which suggest the possibility of Parkinson Disease. We have tried to reinforce iRBD as a marker of neurodegenerative disease and suggest SPECT with TRODAT as an easy method in our country to follow longitudinally these patients.
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spelling pubmed-60560682018-08-06 TRODAT SPECT in patients with idiopathic REM sleep behaviour disorder Rizzo, Geraldo Nunes Vieira Sleep Sci Short Communication to determine the value of dopamine transporter (DAT) neuroimaging radiotracer in a group of idiopathic rapid eye movement sleep behavior disorder (iRBD) patients regarding the development of a synucleinopathy. Methods: 6 retrospectively selected patients with clinical and polysomnographic diagnosis of iRBD, on treatment or not, were submitted to a single-photon emission computerized tomography (SPECT) with TRODAT. Results: Five from six patients have an abnormal test showing reduction in DAT density measured by the linkage potential on SPECT. Conclusions: TRODAT crosses the blood brain barrier, has a high affinity for DAT and is capture by SPECT. The decreased uptake of DAT tracers means a reduction in dopaminergic activity which suggest the possibility of Parkinson Disease. We have tried to reinforce iRBD as a marker of neurodegenerative disease and suggest SPECT with TRODAT as an easy method in our country to follow longitudinally these patients. Brazilian Association of Sleep and Latin American Federation of Sleep 2018 /pmc/articles/PMC6056068/ /pubmed/30083292 http://dx.doi.org/10.5935/1984-0063.20180014 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Rizzo, Geraldo Nunes Vieira
TRODAT SPECT in patients with idiopathic REM sleep behaviour disorder
title TRODAT SPECT in patients with idiopathic REM sleep behaviour disorder
title_full TRODAT SPECT in patients with idiopathic REM sleep behaviour disorder
title_fullStr TRODAT SPECT in patients with idiopathic REM sleep behaviour disorder
title_full_unstemmed TRODAT SPECT in patients with idiopathic REM sleep behaviour disorder
title_short TRODAT SPECT in patients with idiopathic REM sleep behaviour disorder
title_sort trodat spect in patients with idiopathic rem sleep behaviour disorder
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056068/
https://www.ncbi.nlm.nih.gov/pubmed/30083292
http://dx.doi.org/10.5935/1984-0063.20180014
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