van Rooden S M, Visser M, Verbaan D, Marinus J, van Hilten J J
Department of Neurology, K5Q-92, Leiden University Medical Centre, PO Box 9600, NL-2300 RC Leiden, The Netherlands.
J Neurol Neurosurg Psychiatry. 2009 Aug;80(8):846-50. doi: 10.1136/jnnp.2008.166629. Epub 2009 Feb 11.
To evaluate the presence and nature of patterns of coherency among the motor and non-motor domains in Parkinson's disease (PD) and to examine which clinical parameters are related to the potential patterns.
A cohort of 397 patients with PD were randomly divided into two samples. Exploratory factor analysis (EFA) was performed on the motor and non-motor symptoms in PD in the first sample. Findings of the EFA were used to construct a model which was tested in the second sample by confirmatory factor analysis. Multiple regression analyses on the resulting factors were performed to evaluate the influence of clinical parameters on these factors.
Four factors were identified. The first and strongest factor (cognitive impairment, autonomic dysfunction, psychotic symptoms, depression, daytime sleepiness and axial symptoms) reflected advancing disease. Another factor largely reflected motor complications of therapy and was related to dopaminergic medication. The other two factors reflected sleep/depression and tremor/bradykinesia/rigidity, and were only marginally related to disease severity or medication.
The motor and non-motor features in PD can be characterised by four distinct patterns of coherency, which provide insight into the contributions of the primary disease process and antiparkinsonian medication to the broad clinical spectrum of PD. One factor, consisting of predominantly non-motor symptoms together with axial features, clearly reflected disease severity and may provide a new basis for monitoring disease progression in PD.
评估帕金森病(PD)运动和非运动领域连贯性模式的存在及性质,并研究哪些临床参数与潜在模式相关。
将397例PD患者队列随机分为两个样本。对第一个样本中的PD运动和非运动症状进行探索性因子分析(EFA)。EFA的结果用于构建一个模型,并在第二个样本中通过验证性因子分析进行检验。对所得因子进行多元回归分析,以评估临床参数对这些因子的影响。
确定了四个因子。第一个也是最强的因子(认知障碍、自主神经功能障碍、精神症状、抑郁、日间嗜睡和轴性症状)反映疾病进展。另一个因子主要反映治疗的运动并发症,且与多巴胺能药物有关。另外两个因子反映睡眠/抑郁以及震颤/运动迟缓/强直,仅与疾病严重程度或药物有微弱关联。
PD的运动和非运动特征可由四种不同的连贯性模式来表征,这有助于深入了解原发性疾病过程和抗帕金森药物对PD广泛临床谱的影响。一个主要由非运动症状和轴性特征组成的因子清楚地反映了疾病严重程度,可能为监测PD疾病进展提供新的依据。