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Disentangling nigral and putaminal contribution to motor impairment and levodopa response in Parkinson’s disease

The extent to which the degeneration of the substantia nigra (SN) and putamen each contribute to motor impairment in Parkinson’s disease (PD) is unclear, as they are usually investigated using different imaging modalities. To examine the pathophysiological significance of the SN and putamen in both...

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Autores principales: Schröter, Nils, Rijntjes, Michel, Urbach, Horst, Weiller, Cornelius, Treppner, Martin, Kellner, Elias, Jost, Wolfgang H., Sajonz, Bastian E. A., Reisert, Marco, Hosp, Jonas A., Rau, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9568583/
https://www.ncbi.nlm.nih.gov/pubmed/36241644
http://dx.doi.org/10.1038/s41531-022-00401-z
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author Schröter, Nils
Rijntjes, Michel
Urbach, Horst
Weiller, Cornelius
Treppner, Martin
Kellner, Elias
Jost, Wolfgang H.
Sajonz, Bastian E. A.
Reisert, Marco
Hosp, Jonas A.
Rau, Alexander
author_facet Schröter, Nils
Rijntjes, Michel
Urbach, Horst
Weiller, Cornelius
Treppner, Martin
Kellner, Elias
Jost, Wolfgang H.
Sajonz, Bastian E. A.
Reisert, Marco
Hosp, Jonas A.
Rau, Alexander
author_sort Schröter, Nils
collection PubMed
description The extent to which the degeneration of the substantia nigra (SN) and putamen each contribute to motor impairment in Parkinson’s disease (PD) is unclear, as they are usually investigated using different imaging modalities. To examine the pathophysiological significance of the SN and putamen in both motor impairment and the levodopa response in PD using diffusion microstructure imaging (DMI). In this monocentric retrospective cross-sectional study, DMI parameters from 108 patients with PD and 35 healthy controls (HC) were analyzed using a voxel- and region-based approach. Linear models were applied to investigate the association between individual DMI parameters and Movement Disorder Society Unified Parkinson’s Disease Rating Scale-Part 3 performance in ON- and OFF-states, as well as the levodopa response, controlling for age and sex. Voxel- and region-based group comparisons of DMI parameters between PD and HC revealed significant differences in the SN and putamen. In PD, a poorer MDS-UPDRS-III performance in the ON-state was associated with increased free fluid in the SN (b-weight = 65.79, p = 0.004) and putamen (b-weight = 86.00, p = 0.006), and contrariwise with the demise of cells in both structures. The levodopa response was inversely associated with free fluid both in the SN (b-weight = −83.61, p = 0.009) and putamen (b-weight = −176.56, p < 0.001). Interestingly, when the two structures were assessed together, the integrity of the putamen, but not the SN, served as a predictor for the levodopa response (b-weight = −158.03, p < 0.001). Structural alterations in the SN and putamen can be measured by diffusion microstructure imaging in PD. They are associated with poorer motor performance in the ON-state, as well as a reduced response to levodopa. While both nigral and putaminal integrity are required for good performance in the ON-state, it is putaminal integrity alone that determines the levodopa response. Therefore, the structural integrity of the putamen is crucial for the improvement of motor symptoms to dopaminergic medication, and might therefore serve as a promising biomarker for motor staging.
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spelling pubmed-95685832022-10-16 Disentangling nigral and putaminal contribution to motor impairment and levodopa response in Parkinson’s disease Schröter, Nils Rijntjes, Michel Urbach, Horst Weiller, Cornelius Treppner, Martin Kellner, Elias Jost, Wolfgang H. Sajonz, Bastian E. A. Reisert, Marco Hosp, Jonas A. Rau, Alexander NPJ Parkinsons Dis Article The extent to which the degeneration of the substantia nigra (SN) and putamen each contribute to motor impairment in Parkinson’s disease (PD) is unclear, as they are usually investigated using different imaging modalities. To examine the pathophysiological significance of the SN and putamen in both motor impairment and the levodopa response in PD using diffusion microstructure imaging (DMI). In this monocentric retrospective cross-sectional study, DMI parameters from 108 patients with PD and 35 healthy controls (HC) were analyzed using a voxel- and region-based approach. Linear models were applied to investigate the association between individual DMI parameters and Movement Disorder Society Unified Parkinson’s Disease Rating Scale-Part 3 performance in ON- and OFF-states, as well as the levodopa response, controlling for age and sex. Voxel- and region-based group comparisons of DMI parameters between PD and HC revealed significant differences in the SN and putamen. In PD, a poorer MDS-UPDRS-III performance in the ON-state was associated with increased free fluid in the SN (b-weight = 65.79, p = 0.004) and putamen (b-weight = 86.00, p = 0.006), and contrariwise with the demise of cells in both structures. The levodopa response was inversely associated with free fluid both in the SN (b-weight = −83.61, p = 0.009) and putamen (b-weight = −176.56, p < 0.001). Interestingly, when the two structures were assessed together, the integrity of the putamen, but not the SN, served as a predictor for the levodopa response (b-weight = −158.03, p < 0.001). Structural alterations in the SN and putamen can be measured by diffusion microstructure imaging in PD. They are associated with poorer motor performance in the ON-state, as well as a reduced response to levodopa. While both nigral and putaminal integrity are required for good performance in the ON-state, it is putaminal integrity alone that determines the levodopa response. Therefore, the structural integrity of the putamen is crucial for the improvement of motor symptoms to dopaminergic medication, and might therefore serve as a promising biomarker for motor staging. Nature Publishing Group UK 2022-10-14 /pmc/articles/PMC9568583/ /pubmed/36241644 http://dx.doi.org/10.1038/s41531-022-00401-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Schröter, Nils
Rijntjes, Michel
Urbach, Horst
Weiller, Cornelius
Treppner, Martin
Kellner, Elias
Jost, Wolfgang H.
Sajonz, Bastian E. A.
Reisert, Marco
Hosp, Jonas A.
Rau, Alexander
Disentangling nigral and putaminal contribution to motor impairment and levodopa response in Parkinson’s disease
title Disentangling nigral and putaminal contribution to motor impairment and levodopa response in Parkinson’s disease
title_full Disentangling nigral and putaminal contribution to motor impairment and levodopa response in Parkinson’s disease
title_fullStr Disentangling nigral and putaminal contribution to motor impairment and levodopa response in Parkinson’s disease
title_full_unstemmed Disentangling nigral and putaminal contribution to motor impairment and levodopa response in Parkinson’s disease
title_short Disentangling nigral and putaminal contribution to motor impairment and levodopa response in Parkinson’s disease
title_sort disentangling nigral and putaminal contribution to motor impairment and levodopa response in parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9568583/
https://www.ncbi.nlm.nih.gov/pubmed/36241644
http://dx.doi.org/10.1038/s41531-022-00401-z
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