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Basic clinical features do not predict dopamine transporter binding in idiopathic REM behavior disorder

REM sleep behavior disorder (RBD) is strongly associated with development of Parkinson’s Disease and other α-synuclein-related disorders. Dopamine transporter (DAT) binding deficit predicts conversion to α-synuclein-related disorders in individuals with RBD. In turn, identifying which individuals wi...

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Autores principales: Chahine, L. M., Iranzo, A., Fernández-Arcos, A., Simuni, T., Seedorff, N., Caspell-Garcia, C., Amara, A. W., Comella, C., Högl, B., Hamilton, J., Marek, K., Mayer, G., Mollenhauer, B., Postuma, R., Tolosa, E., Trenkwalder, C., Videnovic, A., Oertel, W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351563/
https://www.ncbi.nlm.nih.gov/pubmed/30701189
http://dx.doi.org/10.1038/s41531-018-0073-1
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author Chahine, L. M.
Iranzo, A.
Fernández-Arcos, A.
Simuni, T.
Seedorff, N.
Caspell-Garcia, C.
Amara, A. W.
Comella, C.
Högl, B.
Hamilton, J.
Marek, K.
Mayer, G.
Mollenhauer, B.
Postuma, R.
Tolosa, E.
Trenkwalder, C.
Videnovic, A.
Oertel, W.
author_facet Chahine, L. M.
Iranzo, A.
Fernández-Arcos, A.
Simuni, T.
Seedorff, N.
Caspell-Garcia, C.
Amara, A. W.
Comella, C.
Högl, B.
Hamilton, J.
Marek, K.
Mayer, G.
Mollenhauer, B.
Postuma, R.
Tolosa, E.
Trenkwalder, C.
Videnovic, A.
Oertel, W.
author_sort Chahine, L. M.
collection PubMed
description REM sleep behavior disorder (RBD) is strongly associated with development of Parkinson’s Disease and other α-synuclein-related disorders. Dopamine transporter (DAT) binding deficit predicts conversion to α-synuclein-related disorders in individuals with RBD. In turn, identifying which individuals with RBD have the highest likelihood of having abnormal DAT binding would be useful. The objective of this analysis was to examine if there are basic clinical predictors of DAT deficit in RBD. Participants referred for inclusion in the RBD cohort of the Parkinson Progression Markers Initiative were included. Assessments at the screening visit including DAT SPECT imaging, physical examination, cognitive function screen, and questionnaire-based non-motor assessment. The group with DAT binding deficit (n = 49) was compared to those without (n = 26). There were no significant differences in demographic or clinical features between the two groups. When recruiting RBD cohorts enriched for high risk of neurodegenerative disorders, our data support the need for objective biomarker assessments.
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spelling pubmed-63515632019-01-30 Basic clinical features do not predict dopamine transporter binding in idiopathic REM behavior disorder Chahine, L. M. Iranzo, A. Fernández-Arcos, A. Simuni, T. Seedorff, N. Caspell-Garcia, C. Amara, A. W. Comella, C. Högl, B. Hamilton, J. Marek, K. Mayer, G. Mollenhauer, B. Postuma, R. Tolosa, E. Trenkwalder, C. Videnovic, A. Oertel, W. NPJ Parkinsons Dis Article REM sleep behavior disorder (RBD) is strongly associated with development of Parkinson’s Disease and other α-synuclein-related disorders. Dopamine transporter (DAT) binding deficit predicts conversion to α-synuclein-related disorders in individuals with RBD. In turn, identifying which individuals with RBD have the highest likelihood of having abnormal DAT binding would be useful. The objective of this analysis was to examine if there are basic clinical predictors of DAT deficit in RBD. Participants referred for inclusion in the RBD cohort of the Parkinson Progression Markers Initiative were included. Assessments at the screening visit including DAT SPECT imaging, physical examination, cognitive function screen, and questionnaire-based non-motor assessment. The group with DAT binding deficit (n = 49) was compared to those without (n = 26). There were no significant differences in demographic or clinical features between the two groups. When recruiting RBD cohorts enriched for high risk of neurodegenerative disorders, our data support the need for objective biomarker assessments. Nature Publishing Group UK 2019-01-29 /pmc/articles/PMC6351563/ /pubmed/30701189 http://dx.doi.org/10.1038/s41531-018-0073-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chahine, L. M.
Iranzo, A.
Fernández-Arcos, A.
Simuni, T.
Seedorff, N.
Caspell-Garcia, C.
Amara, A. W.
Comella, C.
Högl, B.
Hamilton, J.
Marek, K.
Mayer, G.
Mollenhauer, B.
Postuma, R.
Tolosa, E.
Trenkwalder, C.
Videnovic, A.
Oertel, W.
Basic clinical features do not predict dopamine transporter binding in idiopathic REM behavior disorder
title Basic clinical features do not predict dopamine transporter binding in idiopathic REM behavior disorder
title_full Basic clinical features do not predict dopamine transporter binding in idiopathic REM behavior disorder
title_fullStr Basic clinical features do not predict dopamine transporter binding in idiopathic REM behavior disorder
title_full_unstemmed Basic clinical features do not predict dopamine transporter binding in idiopathic REM behavior disorder
title_short Basic clinical features do not predict dopamine transporter binding in idiopathic REM behavior disorder
title_sort basic clinical features do not predict dopamine transporter binding in idiopathic rem behavior disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351563/
https://www.ncbi.nlm.nih.gov/pubmed/30701189
http://dx.doi.org/10.1038/s41531-018-0073-1
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