Characterization of de novo Dementia with Lewy Body with different duration of rapid eye movement sleep behavior disorder

路易氏体型失智症 帕金森病 快速眼动睡眠行为障碍 医学 快速眼动睡眠 神经心理学 多导睡眠图 痴呆 路易体 神经学 儿科 内科学 认知 眼球运动 精神科 眼科 疾病 脑电图
作者
Lixin Liu,Zhihong Shi,Jinghuan Gan,Shuai Liu,Wen Chen,Yaqi Yang,Fan Yang,Yong Ji
出处
期刊:Sleep Medicine [Elsevier BV]
卷期号:114: 101-108 被引量:1
标识
DOI:10.1016/j.sleep.2023.12.025
摘要

Cognitive disorder, parkinsonism, autonomic dysfunction (AuD) and rapid eye movement sleep behavior disorder (RBD) can occur prior to or simultaneously with Dementia with Lewy Body (DLB) onset. RBD is generally linked with progressive neurodegenerative traits. However, associations between RBD with DLB, RBD without DLB, and RBD duration effects on DLB symptoms remain unclear. To examine DLB symptom frequency and subtypes in RBD, and explore the effects of different RBD onset times on symptoms in de novo DLB patients. In this multicenter investigation, we consecutively recruited 271 de novo DLB patients. All had standardized clinical and comprehensive neuropsychological evaluations. Subgroup analyses, performed based on the duration of RBD confirmed by polysomnography before the DLB diagnosis, we compared the proportion of patients with cognitive impairment, parkinsonism, and AuD features between groups. Parkinsonism and AuD incidences were significantly elevated in DLB patients with RBD when compared with patients without RBD. Subgroup analyses indicated no significant differences in parkinsonism between DLB patients who developed RBD ≥10 years prior to the DLB diagnosis and DLB patients without RBD. The incidence of non-tremor-predominant parkinsonism and AuD was significantly higher in DLB patients whose RBD duration before the DLB diagnosis was <10 years when compared with DLB patients without RBD. We identified significant symptom and phenotypic variability between DLB patients with and without RBD. Also, different RBD duration effects before the DLB diagnosis had a significant impact on symptomatic phenotypes, suggesting the existence of a slowly progressive DLB neurodegenerative subtype.
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