Lee Seon-Min, Kim Minjik, Lee Hye Mi, Kwon Kyum-Yil, Koh Seong-Beom
Department of Neurology, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Department of Neurology, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
J Neurol Sci. 2015 Feb 15;349(1-2):168-73. doi: 10.1016/j.jns.2015.01.012. Epub 2015 Jan 13.
Recently, the definition of essential tremor (ET) has evolved to have two different meanings. One refers to classic ET, a benign mono-symptomatic disorder, and the other refers to a heterogeneous neurodegenerative disorder. The aim of this study was to categorize nonmotor symptoms according to ET phenotype, and compare them, along with autonomic function, in people with Parkinson's disease (PD) and normal controls.
We divided patients with ET into 3 subtypes according to their motor features: 23 Pure-ET, 25 Cerebellar-ET, and 12 Parkinsonism-ET. Comparisons were made between 30 PD subjects and 22 normal controls, and 60 subjects with ET. The following assessments were conducted: the Nonmotor Symptoms Scale, the Mini-Mental State Exam, Montreal Cognitive Assessment, the Montgomery-Asberg Depression Rating Scale, Neuropsychiatric Inventory Questionnaire, Beck Anxiety Inventory, the Pittsburgh Sleep Quality Index, Epworth Sleepiness Scale and the Scales for Outcomes in Parkinson's Disease-Autonomic.
There were significant differences in the Nonmotor Symptoms Scale total scores of the ET, PD, and control groups (ET: 25.500 ± 2.346; PD: 27.960 ± 3.267;
3.328 ± 3.796.). There were no significant differences in terms of each ET phenotype. ET patients had significant cognitive dysfunction, neuropsychiatric problems including depression and have complained about significant autonomic dysfunction and excessive daytime somnolence compared to normal controls.
Patients with ET have several nonmotor symptoms similar to those of patients with PD, which have a similar impact on their quality of life. Therefore, nonmotor symptoms should be considered in the clinical evaluation and management of ET.
最近,特发性震颤(ET)的定义已演变为具有两种不同含义。一种指经典特发性震颤,一种良性单症状疾病,另一种指异质性神经退行性疾病。本研究的目的是根据ET表型对非运动症状进行分类,并在帕金森病(PD)患者和正常对照者中,将其与自主神经功能进行比较。
我们根据运动特征将ET患者分为3个亚型:23例纯ET型、25例小脑型ET和12例帕金森叠加型ET。对30例PD患者、22例正常对照者和60例ET患者进行了比较。进行了以下评估:非运动症状量表、简易精神状态检查、蒙特利尔认知评估、蒙哥马利-艾斯伯格抑郁评定量表、神经精神科问卷、贝克焦虑量表、匹兹堡睡眠质量指数、爱泼华嗜睡量表和帕金森病自主神经功能结局量表。
ET组、PD组和对照组的非运动症状量表总分存在显著差异(ET组:25.500±2.346;PD组:27.960±3.267;对照组:3.328±3.796)。各ET表型之间无显著差异。与正常对照者相比,ET患者存在明显的认知功能障碍、包括抑郁在内的神经精神问题,且主诉有明显的自主神经功能障碍和日间过度嗜睡。
ET患者有几种与PD患者相似的非运动症状,这些症状对他们的生活质量有类似影响。因此,在ET的临床评估和管理中应考虑非运动症状。