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

被引:0
作者
Dagay, Andrew [1 ,2 ]
Oz, Shani [2 ,3 ]
Katzav, Shlomit [4 ]
Wasserman, Danielle [4 ]
Tauman, Riva [1 ,4 ,5 ]
Thaler, Avner [1 ,2 ,5 ]
Giladi, Nir [1 ,4 ,5 ]
Mirelman, Anat [1 ,2 ,5 ]
机构
[1] Tel Aviv Univ, Sagol Sch Neurosci, Tel Aviv, Israel
[2] Tel Aviv Sourasky Med, Lab Early Markers Neurodegenerat LEMON, Neurol Inst, Tel Aviv, Israel
[3] Tel Aviv Univ, Dept Biomed Engn, Tel Aviv, Israel
[4] Tel Aviv Sourasky Med Ctr, Sieratzki Sagol Inst Sleep Med, Tel Aviv, Israel
[5] Tel Aviv Univ, Fac Med, Tel Aviv, Israel
关键词
Parkinson's disease; sleep; rapid eye movement sleep behavior disorder; sleep disorders; REM sleep without atonia; REM density; TO-NIGHT VARIABILITY; EYE-MOVEMENT DENSITY; BEHAVIOR DISORDER; MOTOR CORTEX; ACTIVATION; ATONIA; YOUNG;
D O I
10.3233/JPD-230116
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:1213 / 1223
页数:11
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