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      Articulatory undershoot of vowels in isolated REM sleep behavior disorder and early Parkinson’s disease

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          Abstract

          Imprecise vowels represent a common deficit associated with hypokinetic dysarthria resulting from a reduced articulatory range of motion in Parkinson’s disease (PD). It is not yet unknown whether the vowel articulation impairment is already evident in the prodromal stages of synucleinopathy. We aimed to assess whether vowel articulation abnormalities are present in isolated rapid eye movement sleep behaviour disorder (iRBD) and early-stage PD. A total of 180 male participants, including 60 iRBD, 60 de-novo PD and 60 age-matched healthy controls performed reading of a standardized passage. The first and second formant frequencies of the corner vowels /a/, /i/, and /u/ extracted from predefined words, were utilized to construct articulatory-acoustic measures of Vowel Space Area (VSA) and Vowel Articulation Index (VAI). Compared to controls, VSA was smaller in both iRBD ( p = 0.01) and PD ( p = 0.001) while VAI was lower only in PD ( p = 0.002). iRBD subgroup with abnormal olfactory function had smaller VSA compared to iRBD subgroup with preserved olfactory function ( p = 0.02). In PD patients, the extent of bradykinesia and rigidity correlated with VSA ( r = −0.33, p = 0.01), while no correlation between axial gait symptoms or tremor and vowel articulation was detected. Vowel articulation impairment represents an early prodromal symptom in the disease process of synucleinopathy. Acoustic assessment of vowel articulation may provide a surrogate marker of synucleinopathy in scenarios where a single robust feature to monitor the dysarthria progression is needed.

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          MDS clinical diagnostic criteria for Parkinson's disease.

          This document presents the Movement Disorder Society Clinical Diagnostic Criteria for Parkinson's disease (PD). The Movement Disorder Society PD Criteria are intended for use in clinical research but also may be used to guide clinical diagnosis. The benchmark for these criteria is expert clinical diagnosis; the criteria aim to systematize the diagnostic process, to make it reproducible across centers and applicable by clinicians with less expertise in PD diagnosis. Although motor abnormalities remain central, increasing recognition has been given to nonmotor manifestations; these are incorporated into both the current criteria and particularly into separate criteria for prodromal PD. Similar to previous criteria, the Movement Disorder Society PD Criteria retain motor parkinsonism as the core feature of the disease, defined as bradykinesia plus rest tremor or rigidity. Explicit instructions for defining these cardinal features are included. After documentation of parkinsonism, determination of PD as the cause of parkinsonism relies on three categories of diagnostic features: absolute exclusion criteria (which rule out PD), red flags (which must be counterbalanced by additional supportive criteria to allow diagnosis of PD), and supportive criteria (positive features that increase confidence of the PD diagnosis). Two levels of certainty are delineated: clinically established PD (maximizing specificity at the expense of reduced sensitivity) and probable PD (which balances sensitivity and specificity). The Movement Disorder Society criteria retain elements proven valuable in previous criteria and omit aspects that are no longer justified, thereby encapsulating diagnosis according to current knowledge. As understanding of PD expands, the Movement Disorder Society criteria will need continuous revision to accommodate these advances.
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            Staging of brain pathology related to sporadic Parkinson’s disease

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              Risk and predictors of dementia and parkinsonism in idiopathic REM sleep behaviour disorder: a multicentre study

              See Morris and Weil (doi:10.1093/brain/awz014) for a scientific commentary on this article. In a prospective multicentre study involving 1280 patients with idiopathic RBD, Postuma et al. show that approximately 6% of patients each year (>73.5% over 12 years) convert to full neurodegenerative disease. They test the predictive power of 21 prodromal markers of neurodegeneration, providing a template for planning neuroprotective trials.
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                Author and article information

                Contributors
                tykalova.tereza@gmail.com
                Journal
                NPJ Parkinsons Dis
                NPJ Parkinsons Dis
                NPJ Parkinson's Disease
                Nature Publishing Group UK (London )
                2373-8057
                20 October 2022
                20 October 2022
                2022
                : 8
                : 137
                Affiliations
                [1 ]GRID grid.411798.2, ISNI 0000 0000 9100 9940, Department of Neurology and Centre of Clinical Neuroscience, First Faculty of Medicine, , Charles University and General University Hospital, ; Prague, Czech Republic
                [2 ]GRID grid.6652.7, ISNI 0000000121738213, Department of Circuit Theory, Faculty of Electrical Engineering, , Czech Technical University in Prague, ; Prague, Czech Republic
                [3 ]GRID grid.5734.5, ISNI 0000 0001 0726 5157, Department of Neurology & ARTORG Center, Inselspital, Bern University Hospital, , University of Bern, ; Bern, Switzerland
                Author information
                http://orcid.org/0000-0002-1036-3054
                http://orcid.org/0000-0001-5608-4029
                http://orcid.org/0000-0002-4893-9661
                http://orcid.org/0000-0003-1156-3709
                Article
                407
                10.1038/s41531-022-00407-7
                9584921
                36266347
                ae0f73c2-0a5b-4309-bd30-89f5eee6f8b3
                © The Author(s) 2022

                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/.

                History
                : 13 April 2022
                : 4 October 2022
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100003243, Ministerstvo Zdravotnictví Ceské Republiky (Ministry of Health of the Czech Republic);
                Award ID: NU20-08-00445
                Award ID: MH CZ–DRO-VFN64165
                Award ID: NU20-08-00445
                Award ID: NU20-08-00445
                Award ID: NU20-08-00445
                Award Recipient :
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                © The Author(s) 2022

                parkinson's disease,olfactory system
                parkinson's disease, olfactory system

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