Citation

Ferini-Strambi L, Rinaldi F, Giora E, Marelli S, Galbiati A. Parkinsonism Relat. Disord. 2015; 22 Suppl 1: S69-72.

Affiliation

Department of Clinical Neurosciences, Neurology-Sleep Disorder Center, San Raffaele Scientific Institute, 20127, Milan, Italy; Vita-Salute San Raffaele University, Faculty of Psychology, Milan, Italy.

Copyright

(Copyright © 2015, Elsevier Publishing)

DOI

10.1016/j.parkreldis.2015.09.002

PMID

26427638

Abstract

Rapid Eye Movement (REM) sleep Behaviour Disorder (RBD) is a REM sleep parasomnia characterized by loss of the muscle atonia that typically occurs during REM sleep, therefore allowing patients to act out their dreams. RBD manifests itself clinically as a violent behaviour occurring during the night, and is detected at the polysomnography by phasic and/or tonic muscle activity on the electromyography channel. In absence of neurological signs or central nervous system lesions, RBD is defined as idiopathic. Nevertheless, in a large number of cases the development of neurodegenerative diseases in RBD patients has been described, with the duration of the follow-up representing a fundamental aspect. A growing number of clinical, neurophysiologic and neuropsychological studies aimed to detect early markers of neurodegenerative dysfunction in RBD patients. Anyway, the evidence of impaired cortical activity, subtle neurocognitive dysfunction, olfactory and autonomic impairment and neuroimaging brain changes in RBD patients is challenging the concept of an idiopathic form of RBD, supporting the idea of RBD as an early manifestation of a more complex neurodegenerative process.

Language: en