4.5 Review

Considering REM Sleep Behavior Disorder in the Management of Parkinson's Disease

Journal

NATURE AND SCIENCE OF SLEEP
Volume 15, Issue -, Pages 333-352

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/NSS.S266071

Keywords

Parkinson's disease; REM sleep behavior disorder; synucleinopathy; biomarkers; neurodegeneration

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Rapid eye movement (REM) sleep behavior disorder (RBD) is characterized by dream-enacting behavior due to the loss of muscle tone inhibition during REM sleep and is considered a precursor to neurodegenerative diseases. Patients with isolated RBD (iRBD) have a high risk of developing a neurodegenerative disease. RBD occurring in the context of Parkinson's disease (PDRBD) identifies a more severe phenotype with increased cognitive decline and treatment options remain limited.
Rapid eye movement (REM) sleep behavior disorder (RBD) is the result of the loss of physiological inhibition of muscle tone during REM sleep, characterized by dream-enacting behavior and widely recognized as a prodromal manifestation of alpha-synucleinopathies. Indeed, patients with isolated RBD (iRBD) have an extremely high estimated risk to develop a neurodegenerative disease after a long follow up. Nevertheless, in comparison with PD patients without RBD (PDnoRBD), the occurrence of RBD in the context of PD (PDRBD) seems to identify a unique, more malignant phenotype, characterized by a more severe burden of disease in terms of both motor and non-motor symptoms and increased risk for cognitive decline. However, while some medications (eg, melatonin, clonazepam, etc.) and non-pharmacological options have been found to have some therapeutic benefits on RBD there is no available treatment able to modify the disease course or, at least, slow down the neurodegenerative process underlying phenoconver-sion. In this scenario, the long prodromal phase may allow an early therapeutic window and, therefore, the identification of multimodal biomarkers of disease onset and progression is becoming increasingly crucial. To date, several clinical (motor, cognitive, olfactory, visual, and autonomic features) neurophysiological, neuroimaging, biological (biofluids or tissue biopsy), and genetic biomarkers have been identified and proposed, also in combination, as possible diagnostic or prognostic markers, along with a potential role for some of them as outcome measures and index of treatment response. In this review, we provide an insight into the present knowledge on both existing and future biomarkers of iRBD and highlight the difference with PDRBD and PDnoRBD, including currently available treatment options.

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