Sleep medicine · 2012
Clinical significance of REM sleep behavior disorder in Parkinson's disease.
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Nomura Takashi, Inoue Yuichi, Kagimura Tatsuo, Nakashima Kenji
Аннотация
OBJECTIVE: Rapid eye movement (REM) sleep behavior disorder (RBD) may be a risk factor for dementia development in patients with Parkinson's disease (PD); however, the role of subclinical RBD remains unknown. Patients with PD and clinical RBD, subclinical RBD, or with normal REM sleep were examined in a cross sectional study and a longitudinal follow-up.
METHODS: Interviews regarding RBD symptoms and polysomnographies were performed on 82 PD patients divided into RBD subcategories based on the presence/absence of REM sleep without atonia (RWA) and/or RBD symptoms. Descriptive variables were compared and patients were followed-up longitudinally for 21.4±10.8months.
RESULTS: The existence of RBD, but not subclinical RBD, was associated with orthostatic hypotension and levodopa dose equivalents (LDEs) in patients with PD. Kaplan-Myer curves indicated that the occurrence of dementia in the PD group with clinical RBD was significantly faster than in the PD group with normal REM sleep (p=0.013). A Cox hazard regression analysis revealed that development to PD with dementia was only significantly associated with the presence of clinical RBD (hazard ratio: 14.1, p=0.017).
CONCLUSION: Clinical RBD symptoms, but not subclinical RBD, were associated with the development of dementia in PD.
METHODS: Interviews regarding RBD symptoms and polysomnographies were performed on 82 PD patients divided into RBD subcategories based on the presence/absence of REM sleep without atonia (RWA) and/or RBD symptoms. Descriptive variables were compared and patients were followed-up longitudinally for 21.4±10.8months.
RESULTS: The existence of RBD, but not subclinical RBD, was associated with orthostatic hypotension and levodopa dose equivalents (LDEs) in patients with PD. Kaplan-Myer curves indicated that the occurrence of dementia in the PD group with clinical RBD was significantly faster than in the PD group with normal REM sleep (p=0.013). A Cox hazard regression analysis revealed that development to PD with dementia was only significantly associated with the presence of clinical RBD (hazard ratio: 14.1, p=0.017).
CONCLUSION: Clinical RBD symptoms, but not subclinical RBD, were associated with the development of dementia in PD.
Предметные рубрики MeSH
AgedAged, 80 and overAntiparkinson AgentsAutonomic Nervous SystemBlood PressureCross-Sectional StudiesDementiaDisability EvaluationDose-Response Relationship, DrugFemaleHeartHumansHypotension, OrthostaticKaplan-Meier EstimateLevodopaLongitudinal StudiesMaleMiddle AgedParkinson DiseasePolysomnographyPrognosisProportional Hazards ModelsREM Sleep Behavior DisorderSleep StagesTilt-Table Test