Literature DB >> 33532150

The Relationship of Rapid Eye Movement Sleep Behavior Disorder and Freezing of Gait in Parkinson's Disease.

Chelsea Mae N Nobleza1, Mariah Siddiqui2,1, Parth V Shah3, Prachi Balani4, Angel R Lopez5, Safeera Khan4.   

Abstract

Rapid eye movement sleep behavior disorder (RBD) contributes to injury due to the alteration of the expected atonia during rapid eye movement (REM) sleep. It occurs before the overt signs of Parkinson's disease (PD). The co-expression of PD and RBD is characterized by non-tremor predominant subtype and higher incidence of freezing. Freezing of gait (FOG) is a debilitating symptom seen in PD patients that lead to falls. While this phenomenon is understood poorly, the involvement of the pedunculopontine nucleus (PPN) and the neural circuits that control locomotion and gait have been examined. This network has also the same control for REM sleep and arousal. The close relationship between PD and RBD and FOG's consequences has led us to explore the relationship between RBD and PD with FOG. This review provides an overview of the neural connections that control gait, locomotion, and REM sleep. The neural changes were seen in PD with FOG and RBD, and sensory and motor changes observed in these two diseases. The functional neuroanatomy that controls REM sleep, arousal, and locomotion overlap significantly with multiple neural circuits affected in RBD and PD with FOG. Visual perception dysfunction and motor symptoms that primarily affect gait initiation are common to both patients with RBD and FOG in PD, leading to freezing episodes. Prospective studies should be conducted to elucidate the relationship of RBD and PD with FOG subtype and find innovative treatment approaches and diagnostic tools for PD with FOG.
Copyright © 2020, Nobleza et al.

Entities:  

Keywords:  anticipatory postural adjustment; freezing of gait; gait; parkinson's disease; pedunculopontine nucleus; postural instability; rbd; visuoperceptive abnormalities

Year:  2020        PMID: 33532150      PMCID: PMC7846434          DOI: 10.7759/cureus.12385

Source DB:  PubMed          Journal:  Cureus        ISSN: 2168-8184


  4 in total

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