Overnight Distribution of REM Sleep Features in People with Parkinson’s Disease (PD) and Non-PD Controls

Author:

Dagay Andrew12,Oz Shani23,Katzav Shlomit4,Wasserman Danielle4,Tauman Riva145,Thaler Avner125,Giladi Nir145,Mirelman Anat125

Affiliation:

1. Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel

2. Laboratory for Early Markers of Neurodegeneration (LEMON), Neurological Institute, Tel Aviv Sourasky Medical, Tel Aviv, Israel

3. Department of Biomedical Engineering, Tel Aviv University, Tel Aviv, Israel

4. Sieratzki Sagol Institute for Sleep Medicine, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel

5. Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

Abstract

Background: Rapid eye movement (REM) sleep behavior disorder (RBD) is a leading predictor of Parkinson’s disease (PD). Diagnosis is performed in the sleep laboratory by detecting pathological REM sleep without atonia (RSWA). The evidence on the overnight distribution of RSWA% is conflicting. Objective: To investigate the temporal distribution of the number of ocular movements per REM sleep minute (REM density), and RSWA% in people with PD and non-PD controls. Methods: All participants underwent a single overnight evaluation in a sleep laboratory. Clinical evaluation was performed on a separate day. REM density and RSWA% were compared between PD and controls both across four sleep periods and individual REM cycles. Results: A total of 51 participants with recorded RSWA in polysomnography laboratory were included, 28 with PD aged 64±9 years with a disease duration of 3.3±2.9 years, and 23 controls aged 55±8 years. People with PD had lower REM density and higher RSWA% compared to controls. As expected, REM density was higher towards the morning. In contrast, RSWA% was equally distributed across the night, for both PD and controls. Conclusions: PD pathology affects REM sleep features, but not the overnight distribution of those features. While REM density increased towards the end of the night, RSWA% was equally distributed across the night for both PD and controls. Our findings have clinical implications for diagnosing RBD, as quantification of RSWA% in any sleep cycle is sufficient for reliably evaluating total RSWA% and reduced REM density may be a marker of PD.

Publisher

IOS Press

Subject

Cellular and Molecular Neuroscience,Neurology (clinical)

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