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      Quantitative sensory testing and norepinephrine levels in REM sleep behaviour disorder – a clue to early peripheral autonomic and sensory dysfunction?

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          Abstract

          Introduction

          Studies have reported autonomic impairment in patients with idiopathic REM sleep behaviour disorder (iRBD), which is considered a prodromal stage of alpha-synucleinopathies. It is still debated whether central or peripheral pathologies are first manifestations of alpha-synucleinopathies. This study aimed to characterize autonomic and somatosensory function in iRBD patients.

          Methods

          This cross-sectional prospective case–control study included 17 iRBD patients (mean age 66.3 ± 9.2 years) and 16 healthy controls (HCs, 66.6 ± 11.3 years). Quantitative sensory testing, neurological and neuropsychological assessments, norepinephrine blood plasma levels, tilt table examination with orthostatic blood pressure, and heart rate variability were carried out. Longitudinal data of 10 iRBD patients, including neurological, neuropsychological, and tilt table examination, were assessed.

          Results

          iRBD patients more frequently presented with orthostatic dysfunction than HCs (70.6% vs. 6.3%, p < 0.0001). Supine norepinephrine plasma levels were normal, but lower in iRBD (249.59 ± 99.78 pg/ml iRBD, 354.13 ± 116.38 pg/ml HCs, p < 0.05). Quantitative sensory testing revealed impaired cold (CDT) and vibration detection thresholds (VDT) on the foot in iRBD (CDT foot iRBD − 1.24 ± 0.31, HCs − 9.89E-17 ± 0.25, VDT iRBD − 1.11 ± 0.47, HCs − 1.46E-16 ± 0.25, p < 0.05). Cold detection thresholds differed between the foot and hand among iRBD patients (foot − 1.24 ± 0.31, hand − 0.56 ± 0.25, p < 0.05). Longitudinal data revealed an increase in maximum systolic and diastolic orthostatic blood pressure changes and a decrease in the Valsalva ratio in the follow-up group ( p < 0.05).

          Conclusion

          This study revealed autonomic dysfunction with somatosensory impairment, and decreased norepinephrine levels in iRBD, which may serve as a possible prodromal marker for developing alpha-synucleinopathy.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s00415-021-10675-7.

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          Most cited references33

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          Consensus statement on the definition of orthostatic hypotension, neurally mediated syncope and the postural tachycardia syndrome.

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            New Clinical Subtypes of Parkinson Disease and Their Longitudinal Progression: A Prospective Cohort Comparison With Other Phenotypes.

            There is increasing evidence that Parkinson disease (PD) is heterogeneous in its clinical presentation and prognosis. Defining subtypes of PD is needed to better understand underlying mechanisms, predict disease course, and eventually design more efficient personalized management strategies.
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              REM sleep behavior disorder: Updated review of the core features, the REM sleep behavior disorder-neurodegenerative disease association, evolving concepts, controversies, and future directions.

              Rapid eye movement (REM) sleep behavior disorder (RBD) is a parasomnia manifested by vivid, often frightening dreams associated with simple or complex motor behavior during REM sleep. The polysomnographic features of RBD include increased electromyographic tone +/- dream enactment behavior during REM sleep. Management with counseling and pharmacologic measures is usually straightforward and effective. In this review, the terminology, clinical and polysomnographic features, demographic and epidemiologic features, diagnostic criteria, differential diagnosis, and management strategies are discussed. Recent data on the suspected pathophysiologic mechanisms of RBD are also reviewed. The literature and our institutional experience on RBD are next discussed, with an emphasis on the RBD-neurodegenerative disease association and particularly the RBD-synucleinopathy association. Several issues relating to evolving concepts, controversies, and future directions are then reviewed, with an emphasis on idiopathic RBD representing an early feature of a neurodegenerative disease and particularly an evolving synucleinopathy. Planning for future therapies that impact patients with idiopathic RBD is reviewed in detail.
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                Author and article information

                Contributors
                julkoch@ukaachen.de
                willemsen.kira@gmail.com
                idogan@ukaachen.de
                rrolke@ukaachen.de
                jschulz@ukaachen.de
                jschiefer@ukaachen.de
                kreetz@ukaachen.de
                amaier@ukaachen.de
                Journal
                J Neurol
                J Neurol
                Journal of Neurology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0340-5354
                1432-1459
                25 June 2021
                25 June 2021
                2022
                : 269
                : 2
                : 923-932
                Affiliations
                [1 ]GRID grid.1957.a, ISNI 0000 0001 0728 696X, Department of Neurology, , Medical Faculty RWTH Aachen University, ; Pauwelsstraße 30, D-52074 Aachen, Germany
                [2 ]GRID grid.1957.a, ISNI 0000 0001 0728 696X, JARA-BRAIN Institute Molecular Neuroscience and Neuroimaging, Forschungszentrum Jülich GmbH, , Medical Faculty RWTH Aachen University, ; Pauwelsstraße 30, D-52074 Aachen, Germany
                [3 ]GRID grid.1957.a, ISNI 0000 0001 0728 696X, Department of Palliative Medicine, , Medical Faculty RWTH Aachen University, ; Pauwelsstraße 30, D-52074 Aachen, Germany
                Author information
                http://orcid.org/0000-0002-3427-4806
                Article
                10675
                10.1007/s00415-021-10675-7
                8782803
                34170404
                bb2c91ae-6535-4d81-a1a0-aadc8aaf9b25
                © The Author(s) 2021

                Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 4 February 2021
                : 14 June 2021
                : 14 June 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100009398, Medizinische Fakultät, RWTH Aachen University;
                Award ID: START 124/16
                Award Recipient :
                Funded by: Universitätsklinikum RWTH Aachen (8915)
                Categories
                Original Communication
                Custom metadata
                © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany 2022

                Neurology
                idiopathic rem sleep behaviour disorder,autonomic dysfunction,quantitative sensory testing,norepinephrine levels,somatosensory dysfunction

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