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      Modulatory Effects of Levodopa on Cerebellar Connectivity in Parkinson’s Disease

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          Abstract

          Levodopa has been the mainstay of symptomatic therapy for Parkinson’s disease (PD) for the last five decades. However, it is associated with the development of motor fluctuations and dyskinesia, in particular after several years of treatment. The aim of this study was to shed light on the acute brain functional reorganization in response to a single levodopa dose. Functional magnetic resonance imaging (fMRI) was performed after an overnight withdrawal of dopaminergic treatment and 1 h after a single dose of 250 mg levodopa in a group of 24 PD patients. Eigenvector centrality was calculated in both treatment states using resting-state fMRI. This offers a new data-driven and parameter-free approach, similar to Google’s PageRank algorithm, revealing brain connectivity alterations due to the effect of levodopa treatment. In all PD patients, levodopa treatment led to an improvement of clinical symptoms as measured with the Unified Parkinson’s Disease Rating Scale motor score (UPDRS-III). This therapeutic effect was accompanied with a major connectivity increase between cerebellar brain regions and subcortical areas of the motor system such as the thalamus, putamen, globus pallidus, and brainstem. The degree of interconnectedness of cerebellar regions correlated with the improvement of clinical symptoms due to the administration of levodopa. We observed significant functional cerebellar connectivity reorganization immediately after a single levodopa dose in PD patients. Enhanced general connectivity (eigenvector centrality) was associated with better motor performance as assessed by UPDRS-III score. This underlines the importance of considering cerebellar networks as therapeutic targets in PD.

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          The online version of this article (10.1007/s12311-018-0981-y) contains supplementary material, which is available to authorized users.

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          Most cited references31

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          The cerebellum communicates with the basal ganglia.

          The cerebral cortex is interconnected with two major subcortical structures: the basal ganglia and the cerebellum. How and where cerebellar circuits interact with basal ganglia circuits has been a longstanding question. Using transneuronal transport of rabies virus in macaques, we found that a disynaptic pathway links an output stage of cerebellar processing, the dentate nucleus, with an input stage of basal ganglia processing, the striatum.
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            Regional homogeneity changes in patients with Parkinson's disease.

            Resting state brain activity in Parkinson's disease (PD) can give clues to the pathophysiology of the disorder, and might be helpful in diagnosis, but it has never been explored using functional MRI (fMRI). In the current study, we used a regional homogeneity (ReHo) method to investigate PD-related modulations of neural activity in the resting state. FMRIs were acquired in 22 patients with PD at both before and after levodopa administration, as well as in 22 age- and sex-matched normal controls. In the PD group compared with the healthy controls, we found ReHo decreased in extensive brain regions, including the putamen, thalamus, and supplementary motor area; and increased in some other areas, including the cerebellum, primary sensorimotor cortex, and premotor area. The ReHo off medication was negatively correlated with the Unified Parkinson's Disease Rating Scale (UPDRS) in the putamen and some other regions, and was positively correlated with the UPDRS in the cerebellum. Administration of levodopa relatively normalized ReHo. Our findings demonstrate that neural activity in the resting state is changed in patients with PD. This change is secondary to dopamine deficiency, and related to the severity of the disease. The different neuronal activity at the baseline state should be considered in explaining fMRI findings obtained during tasks. . (c) 2008 Wiley-Liss, Inc.
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              Spatial remapping of cortico-striatal connectivity in Parkinson's disease.

              Parkinson's disease (PD) is characterized by striatal dopamine depletion, especially in the posterior putamen. The dense connectivity profile of the striatum suggests that these local impairments may propagate throughout the whole cortico-striatal network. Here we test the effect of striatal dopamine depletion on cortico-striatal network properties by comparing the functional connectivity profile of the posterior putamen, the anterior putamen, and the caudate nucleus between 41 PD patients and 36 matched controls. We used multiple regression analyses of resting-state functional magnetic resonance imaging data to quantify functional connectivity across different networks. Each region had a distinct connectivity profile that was similarly expressed in patients and controls: the posterior putamen was uniquely coupled to cortical motor areas, the anterior putamen to the pre-supplementary motor area and anterior cingulate cortex, and the caudate nucleus to the dorsal prefrontal cortex. Differences between groups were specific to the putamen: although PD patients showed decreased coupling between the posterior putamen and the inferior parietal cortex, this region showed increased functional connectivity with the anterior putamen. We conclude that dopamine depletion in PD leads to a remapping of cerebral connectivity that reduces the spatial segregation between different cortico-striatal loops. These alterations of network properties may underlie abnormal sensorimotor integration in PD.
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                Author and article information

                Contributors
                karstenm@cbs.mpg.de
                +420 224965556 , jech@cesnet.cz
                Journal
                Cerebellum
                Cerebellum
                Cerebellum (London, England)
                Springer US (New York )
                1473-4222
                1473-4230
                8 October 2018
                8 October 2018
                2019
                : 18
                : 2
                : 212-224
                Affiliations
                [1 ]ISNI 0000 0001 0041 5028, GRID grid.419524.f, Max Planck Institute for Human Cognitive and Brain Sciences, ; Leipzig, Germany
                [2 ]ISNI 0000 0000 9100 9940, GRID grid.411798.2, Department of Neurology - Center for interventional therapy of movement disorders, 1st Faculty of Medicine, , Charles University and General University Hospital in Prague, ; Prague, Czech Republic
                [3 ]ISNI 0000 0004 0609 2583, GRID grid.414877.9, Department of Radiology, , Na Homolce Hospital, ; Prague, Czech Republic
                [4 ]ISNI 0000 0000 8517 9062, GRID grid.411339.d, Clinic for Cognitive Neurology, , University Hospital Leipzig, ; Leipzig, Germany
                Article
                981
                10.1007/s12311-018-0981-y
                6443641
                30298443
                408631ed-dbc3-4782-a10f-ed90cfd9a065
                © The Author(s) 2018

                Open Access This 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.

                History
                Funding
                Funded by: Czech Science Foundation
                Award ID: 16-13323S
                Award Recipient :
                Funded by: Charles University in Prague
                Award ID: PROGRES Q27
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100001288, Parkinson's Disease Foundation;
                Award ID: PDF-IRG-1307
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000864, Michael J. Fox Foundation for Parkinson's Research;
                Award ID: MJFF-11362
                Award Recipient :
                Categories
                Original Paper
                Custom metadata
                © Springer Science+Business Media, LLC, part of Springer Nature 2019

                Neurology
                dopaminergic treatment,l-dopa,levodopa,parkinson’s disease,resting-state magnetic resonance imaging,eigenvector centrality,brain connectivity,functional connectivity,nexopathy,cerebellum,cerebellar networks,brainstem

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