期刊
SLEEP MEDICINE
卷 84, 期 -, 页码 308-316出版社
ELSEVIER
DOI: 10.1016/j.sleep.2021.06.011
关键词
Prediagnostic Parkinson's disease; REM sleep without atonia; REM sleep behavior disorder; Polysomnography; Body position
资金
- Rotary Belgium
- Move for Parkinson
The study found that in the prodromal stages of Parkinson's disease (PD), patients showed higher RSWA variables and a higher percentage of nocturnal supine body position, regardless of RBD status. These results suggest that these PSG abnormalities may serve as prodromal biomarkers for PD.
Background: Sleep disturbances are features of Parkinson's disease (PD), that can already occur before PD diagnosis. The most investigated prodromal PD sleep disorder is REM sleep behavior disorder (RBD). The relation between other polysomnographic (PSG) alterations and the prediagnostic stages of PD, however, is less clear. Methods: We performed a retrospective case-control study to characterize polysomnographic alterations in PD and prediagnostic PD. We included 63 PD subjects (33 subjects that underwent a video-PSG before PD diagnosis [13 with and 20 without RBD] and 30 subjects that underwent a PSG after PD diagnosis) and 30 controls. PSGs were analyzed for sleep stages, different RSWA variables, body position, arousals, periodic limb movements, and REM density. Results: Higher subscores of all RSWA variables were observed in subjects with PD and prediagnostic PD (with and without RBD). Total RSWA, tonic RSWA and chin RSWA severity were significant predictors for all PD and prediagnostic PD groups. Our study also shows a higher percentage of nocturnal supine body position in all PD and prediagnostic PD groups. Supine body position percentage is the highest in the PD group and has a positive correlation with time since diagnosis. Conclusions: These findings suggest that increased total, tonic and chin RSWA as well as nocturnal supine body position are already present in prediagnostic PD, independently of RBD status. Prospective longitudinal studies are necessary to confirm the additional value of these PSG abnormalities as prodromal PD biomarkers. (C) 2021 Elsevier B.V. All rights reserved.
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