Does REM sleep behavior disorder change in the progression of Parkinson's disease?

被引:36
作者
Figorilli, M. [1 ,2 ]
Marques, A. R. [1 ,3 ]
Vidal, T. [4 ]
Delaby, L. [4 ]
Meloni, M. [2 ]
Pereira, B. [5 ]
Lambert, C. [5 ]
Puligheddu, M. [2 ]
Durif, F. [1 ,3 ]
Fantini, M. L. [1 ,3 ]
机构
[1] Univ Clermont Auvergne, UFR Med, EA 7280, Clermont Ferrand, France
[2] Univ Cagliari, Sleep Disorder Ctr, Dept Publ Hlth & Clin & Mol Med, Cagliari, Italy
[3] CHU, Neurol Dept, Clermont Ferrand, France
[4] CHU, CMRR, Clermont Ferrand, France
[5] CHU, Biostat Unit DRCI, Clermont Ferrand, France
关键词
REM sleep behavior disorder; REM sleep without atonia; Parkinson's disease; Longitudinal; Progression; SCALE; VALIDATION; DIAGNOSIS; SEVERITY; DEMENTIA;
D O I
10.1016/j.sleep.2019.12.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives/background: Rapid eye movement (REM) Sleep Behavior Disorder (RBD) in Parkinson's disease (PD) may be associated with a malignant phenotype. Despite its prognostic value, little is known about the time course of RBD in PD. In this study, we aimed to ascertain whether or not RBD is a stable feature in PD. In this study, we prospectively evaluated clinical and neurophysiological features of RBD, including REM Sleep Without Atonia (RSWA), in PD patients with RBD at baseline and after three years then assessed whether the changes in measures of RSWA parallel the progression of PD. Patients/methods: In sum, 22 (17M, mean age 64.0 +/- 6.9 years) moderate-to-advanced PD patients (mean PD duration at baseline:7.6 +/- 4.8 years) with RBD, underwent a video-polysomnography (vPSG) recording and clinical and neuropsychological assessment at baseline and after three years. Results: At follow-up, the self-assessed frequency of RBD symptoms increased in six patients, decreased in six and remained stable in 10, while RSWA measures significantly increased in all subjects. At follow-up, patients showed worse H&Y stage (p = 0.02), higher dopaminergic doses (p = 0.05) and they performed significantly worse in phonetic and semantic fluency tests (p = 0.02; p = 0.04). Changes in RSWA correlated significantly with the severity in levodopa-induced dyskinesia (r = 0.61, p = 0.05) and motor fluctuation (r = 0.54, p = 0.03) scores, and with the worsening of executive functions (r = 0.78, p = 0.001) and visuo-spatial perception (r = -0.57, p = 0.04). Conclusion: Despite the subjective improvement of RBD symptoms in one-fourth of PD patients, all RSWA measures increased significantly at follow-up, and their changes correlated with the clinical evolution of motor and non-motor symptoms. RBD is a long-lasting feature in PD and RSWA is a marker of the disease's progression. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:190 / 198
页数:9
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