Center of Neurology, Department of Neurodegeneration and Hertie Institute for Clinical Brain Research, University of Tuebingen, Tuebingen, Germany; German Center for Neurodegenerative Diseases, University of Tuebingen, Tuebingen, Germany.
Center of Neurology, Department of Neurodegeneration and Hertie Institute for Clinical Brain Research, University of Tuebingen, Tuebingen, Germany; German Center for Neurodegenerative Diseases, University of Tuebingen, Tuebingen, Germany.
Neurobiol Aging. 2018 Oct;70:242-246. doi: 10.1016/j.neurobiolaging.2018.06.029. Epub 2018 Jun 30.
REM sleep behavior disorder (RBD) represents a major and relatively specific prodromal marker for synucleinopathies such as Parkinson's disease (PD), dementia with Lewy bodies, and multisystem atrophy. Because PD patients primarily suffer from executive dysfunction, we hypothesized that individuals with RBD show an impairment in the nonamnestic executive domain rather than in amnestic domains. To address this question, we investigated a cohort of 1145 healthy elderly (183 with RBD) cross-sectionally and a subgroup of 544 of them longitudinally (144 with RBD) over 6 years. Assessments included the RBD screening questionnaire, the extended Consortium to Establish a Registry for Alzheimer's Disease test battery, and genetic testing for the risk variant rs356219 in the alpha-synuclein gene. In the cross-sectional analysis, the RBD subgroup showed worse performance in the Trail Making Test (TMT) part B and the delta-TMT_B-A when compared to non-RBD subjects. Longitudinal observation revealed a deterioration of TMT-B and delta-TMT_B-A in RBD subjects, a phenomenon that was not observed in the group of non-RBD subjects. These data argue for an early and progressive deterioration of executive dysfunction associated with RBD. Of the total cohort, 18 developed Parkinsonism including 16 with sporadic PD after a mean follow-up of 4.6 years. Of the sporadic PD cases, 4.4% were from the probable RBD group and 0.8% of the non-RBD group. The potential of this dynamic for the detection of prodromal synucleinopathies seems relevant, but has to be determined in studies including converters.
快速眼动睡眠行为障碍(RBD)是一种主要的、相对特异的突触核蛋白病(如帕金森病、路易体痴呆和多系统萎缩)的前驱标志物。由于帕金森病患者主要表现为执行功能障碍,我们假设 RBD 患者在非遗忘执行域存在障碍,而不是在遗忘域存在障碍。为了回答这个问题,我们对 1145 名健康老年人(183 名有 RBD)进行了横断面研究,并对其中 544 名(144 名有 RBD)进行了 6 年的纵向研究。评估包括 RBD 筛查问卷、扩展的阿尔茨海默病协会注册研究测试组合,以及 alpha-突触核蛋白基因风险变异 rs356219 的基因检测。在横断面分析中,与非 RBD 组相比,RBD 组在连线测试(TMT)B 部分和 delta-TMT_B-A 中表现出更差的表现。纵向观察显示 RBD 组的 TMT-B 和 delta-TMT_B-A 恶化,而非 RBD 组则没有观察到这种现象。这些数据表明与 RBD 相关的执行功能障碍存在早期和进行性恶化。在总队列中,18 人发展为帕金森病,包括 16 例散发性帕金森病,平均随访 4.6 年后。在散发性帕金森病病例中,4.4%来自可能的 RBD 组,0.8%来自非 RBD 组。这种动态检测前驱性突触核蛋白病的潜力似乎是相关的,但需要在包括转化者在内的研究中确定。