Effects of Levodopa on quality of sleep and nocturnal movements in Parkinson's Disease
- PMID: 33544218
- PMCID: PMC8216994
- DOI: 10.1007/s00415-021-10419-7
Effects of Levodopa on quality of sleep and nocturnal movements in Parkinson's Disease
Abstract
Background: Sleep disturbances are common in Parkinson's Disease (PD), with nocturnal akinesia being one of the most burdensome. Levodopa is frequently used in clinical routine to improve nocturnal akinesia, although evidence is not well proven.
Methods: We assessed associations of Levodopa intake with quality of sleep and perception of nocturnal akinesia in three PD cohorts, using the Parkinson's Disease Sleep Scale (PDSS-2) in two cohorts and a question on nocturnal immobility in one cohort. In one cohort also objective assessment of mobility during sleep was performed, using mobile health technology.
Results: In an independent analysis of all three cohorts (in total n = 1124 PD patients), patients taking Levodopa CR reported a significantly higher burden by nocturnal akinesia than patients without Levodopa. Higher Levodopa intake and MDS-UPDRS part IV scores (indicating motor fluctuations) predicted worse PDSS-2 and higher subjective nocturnal immobility scores, while disease duration and severity were not predictive. Levodopa intake was not associated with objectively changed mobility during sleep.
Conclusion: Our results showed an association of higher Levodopa intake with perception of worse quality of sleep and nocturnal immobility in PD, indicating that Levodopa alone might not be suitable to improve subjective feeling of nocturnal akinesia in PD. In contrast, Levodopa intake was not relevantly associated with objectively measured mobility during sleep. PD patients with motor fluctuations may be particularly affected by subjective perception of nocturnal mobility. This study should motivate further pathophysiological and clinical investigations on the cause of perception of immobility during sleep in PD.
Keywords: Hypokinesia; Levodopa; Parkinson Disease; Sleep.
Conflict of interest statement
E. Schaeffer received intramural research funding from the University of Kiel and speaker’s honoraria from Bayer Vital GmbH and Novartis, outside the submitted work. T. Vaterrodt, L. Zaunbrecher, K. Emmert, M. Elsehabi, B. Roeben, C. Hansen, S. Becker, S. Nussbaum and J-H. Busch have nothing to declare. I. Liepelt-Scarfone received an unrestricted research grant from Johnson & Johnson to conduct the ABC-PD study, and grants from the International Parkinson Fonds GmbH IPO, European Commission Horizon 2020, National Center of Excellence in Research, Luxembourg National Research Fund and Michael J Fox Foundation. M. Synofzik received Consultancy Honoraria von Actelion Pharmaceuticals, outside the submitted work. D. Berg reports grants from Janssen Pharmaceutica, grants from the Damp foundation, grants from the German Parkinson’s Disease Association (dPV), grants from BMWi, grants from BMBF, grants from the Parkinson Fonds Deutschland GmbH, grants and speaker’s honoraria from and consultancy honoraria of UCB Pharma GmbH, grants and speaker’s honoraria from TEVA Pharma GmbH, grants from and consultancies for Novartis Pharma GmbH, grants and speaker’s honoraria from and consultancy honoraria of Lundbeck, speaker’s honoraria from and consultancy honoraria for BIAL, speaker’s honoraria from and consultancy honoraria for Biogen, honoraria from Bayer and Zambon outside the submitted work. W. Maetzler receives or received funding from the European Union, the German Federal Ministry of Education of Research, Neuroalliance, Lundbeck and Janssen. He received speaker honoraria from Abbvie, Bayer, GlaxoSmithKline, Licher MT, Pharma, Takeda and UCB, was invited to Advisory Boards of Abbvie, Biogen, Lundbeck and Market Access & Pricing Strategy GmbH, and is an advisory board member of the Critical Path for Parkinson’s Consortium. He serves as the co-chair of the MDS Technology Task Force.
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