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Spatiotemporal patterns of putaminal dopamine processing in Parkinson’s disease: A multi-tracer positron emission tomography study

Alterations in different aspects of dopamine processing may exhibit different progressive behaviours throughout the course of Parkinson’s disease. We used a novel data-driven multivariate approach to quantify and compare spatiotemporal patterns related to different aspects of dopamine processing fro...

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Autores principales: Fu, Jessie Fanglu, Wegener, Tilman, Klyuzhin, Ivan S., Mannheim, Julia G., McKeown, Martin J., Stoessl, A. Jon, Sossi, Vesna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668665/
https://www.ncbi.nlm.nih.gov/pubmed/36451352
http://dx.doi.org/10.1016/j.nicl.2022.103246
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author Fu, Jessie Fanglu
Wegener, Tilman
Klyuzhin, Ivan S.
Mannheim, Julia G.
McKeown, Martin J.
Stoessl, A. Jon
Sossi, Vesna
author_facet Fu, Jessie Fanglu
Wegener, Tilman
Klyuzhin, Ivan S.
Mannheim, Julia G.
McKeown, Martin J.
Stoessl, A. Jon
Sossi, Vesna
author_sort Fu, Jessie Fanglu
collection PubMed
description Alterations in different aspects of dopamine processing may exhibit different progressive behaviours throughout the course of Parkinson’s disease. We used a novel data-driven multivariate approach to quantify and compare spatiotemporal patterns related to different aspects of dopamine processing from cross-sectional Parkinson’s subjects obtained with: 1) 69 [(11)C]±dihydrotetrabenazine (DTBZ) scans, most closely related to dopaminergic denervation; 2) 73 [(11)C]d-threo-methylphenidate (MP) scans, marker of dopamine transporter density; 3) 50 6-[(18)F]fluoro-l-DOPA (FD) scans, marker of dopamine synthesis and storage. The anterior-posterior gradient in the putamen was identified as the most salient feature associated with disease progression, however the temporal progression of the spatial gradient was different for the three tracers. The expression of the anterior-posterior gradient was the highest for FD at disease onset compared to that of DTBZ and MP (P = 0.018 and P = 0.047 respectively), but decreased faster (P = 0.006) compared to that of DTBZ. The gradient expression for MP was initially similar but decreased faster (P = 0.015) compared to that for DTBZ. These results reflected unique temporal behaviours of regulatory mechanisms related to dopamine synthesis (FD) and reuptake (MP). While the relative early disease upregulation of dopamine synthesis in the anterior putamen prevalent likely extends to approximately 10 years after symptom onset, the presumed downregulation of dopamine transporter density may play a compensatory role in the prodromal/earliest disease stages only.
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spelling pubmed-96686652022-11-18 Spatiotemporal patterns of putaminal dopamine processing in Parkinson’s disease: A multi-tracer positron emission tomography study Fu, Jessie Fanglu Wegener, Tilman Klyuzhin, Ivan S. Mannheim, Julia G. McKeown, Martin J. Stoessl, A. Jon Sossi, Vesna Neuroimage Clin Regular Article Alterations in different aspects of dopamine processing may exhibit different progressive behaviours throughout the course of Parkinson’s disease. We used a novel data-driven multivariate approach to quantify and compare spatiotemporal patterns related to different aspects of dopamine processing from cross-sectional Parkinson’s subjects obtained with: 1) 69 [(11)C]±dihydrotetrabenazine (DTBZ) scans, most closely related to dopaminergic denervation; 2) 73 [(11)C]d-threo-methylphenidate (MP) scans, marker of dopamine transporter density; 3) 50 6-[(18)F]fluoro-l-DOPA (FD) scans, marker of dopamine synthesis and storage. The anterior-posterior gradient in the putamen was identified as the most salient feature associated with disease progression, however the temporal progression of the spatial gradient was different for the three tracers. The expression of the anterior-posterior gradient was the highest for FD at disease onset compared to that of DTBZ and MP (P = 0.018 and P = 0.047 respectively), but decreased faster (P = 0.006) compared to that of DTBZ. The gradient expression for MP was initially similar but decreased faster (P = 0.015) compared to that for DTBZ. These results reflected unique temporal behaviours of regulatory mechanisms related to dopamine synthesis (FD) and reuptake (MP). While the relative early disease upregulation of dopamine synthesis in the anterior putamen prevalent likely extends to approximately 10 years after symptom onset, the presumed downregulation of dopamine transporter density may play a compensatory role in the prodromal/earliest disease stages only. Elsevier 2022-10-25 /pmc/articles/PMC9668665/ /pubmed/36451352 http://dx.doi.org/10.1016/j.nicl.2022.103246 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 Regular Article
Fu, Jessie Fanglu
Wegener, Tilman
Klyuzhin, Ivan S.
Mannheim, Julia G.
McKeown, Martin J.
Stoessl, A. Jon
Sossi, Vesna
Spatiotemporal patterns of putaminal dopamine processing in Parkinson’s disease: A multi-tracer positron emission tomography study
title Spatiotemporal patterns of putaminal dopamine processing in Parkinson’s disease: A multi-tracer positron emission tomography study
title_full Spatiotemporal patterns of putaminal dopamine processing in Parkinson’s disease: A multi-tracer positron emission tomography study
title_fullStr Spatiotemporal patterns of putaminal dopamine processing in Parkinson’s disease: A multi-tracer positron emission tomography study
title_full_unstemmed Spatiotemporal patterns of putaminal dopamine processing in Parkinson’s disease: A multi-tracer positron emission tomography study
title_short Spatiotemporal patterns of putaminal dopamine processing in Parkinson’s disease: A multi-tracer positron emission tomography study
title_sort spatiotemporal patterns of putaminal dopamine processing in parkinson’s disease: a multi-tracer positron emission tomography study
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668665/
https://www.ncbi.nlm.nih.gov/pubmed/36451352
http://dx.doi.org/10.1016/j.nicl.2022.103246
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