Litvan I, Campbell G, Mangone C A, Verny M, McKee A, Chaudhuri K R, Jellinger K, Pearce R K, D'Olhaberriague L
Neuroepidemiology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-9130, USA.
Brain. 1997 Jan;120 ( Pt 1):65-74. doi: 10.1093/brain/120.1.65.
The difficulty in differentiating progressive supranuclear palsy (PSP, also called Steele-Richardson-Olszewski syndrome) from other related disorders was the incentive for a study to determine the clinical features that best distinguish PSP. Logistic regression and classification and regression tree analysis (CART) were used to analyse data obtained at the first visit from a sample of 83 patients with a clinical history of parkinsonism or dementia confirmed neuropathologically, including PSP (n = 24), corticobasal degeneration (n = 11), Parkinson's disease (PD, n = 11), diffuse Lewy body disease (n = 14). Pick's disease (n = 8) and multiple system atrophy (MSA, n = 15). Supranuclear vertical gaze palsy, moderate or severe postural instability and falls during the first year after onset of symptoms classified the sample with 9% error using logistic regression analysis. The CART identified similar features and was also helpful in identifying particular attributes that separate PSP from each of the other disorders. Unstable gait, absence of tremor-dominant disease and absence of a response to levodopa differentiated PSP from PD. Supranuclear vertical gaze palsy, gait instability and the absence of delusions distinguished PSP from diffuse Lewy body disease. Supranuclear vertical gaze palsy and increased age at symptom-onset distinguished PSP from MSA. Gait abnormality, severe upward gaze palsy, bilateral bradykinesia and absence of alien limb syndorme separated PSP from corticobasal degeneration. Postural instability successfully classified PSP from Pick's disease. The present study may help to minimize the difficulties neurologists experience when attempting to classify these disorders at early stages.
将进行性核上性麻痹(PSP,也称为Steele-Richardson-Olszewski综合征)与其他相关疾病区分开来存在困难,这促使开展一项研究以确定最能区分PSP的临床特征。采用逻辑回归和分类回归树分析(CART)对首次就诊时从83例经神经病理学确诊有帕金森综合征或痴呆临床病史的患者样本中获取的数据进行分析,这些患者包括PSP(n = 24)、皮质基底节变性(n = 11)、帕金森病(PD,n = 11)、弥漫性路易体病(n = 14)、匹克病(n = 8)和多系统萎缩(MSA,n = 15)。症状出现后第一年内的核上性垂直凝视麻痹、中度或重度姿势不稳和跌倒,使用逻辑回归分析对样本进行分类时误差为9%。CART识别出了类似特征,还有助于识别将PSP与其他每种疾病区分开来的特定属性。步态不稳、无震颤为主型疾病以及对左旋多巴无反应可将PSP与PD区分开来。核上性垂直凝视麻痹、步态不稳和无妄想可将PSP与弥漫性路易体病区分开来。核上性垂直凝视麻痹和症状出现时年龄增加可将PSP与MSA区分开来。步态异常、严重向上凝视麻痹、双侧运动迟缓以及无异己肢体综合征可将PSP与皮质基底节变性区分开来。姿势不稳成功地将PSP与匹克病区分开来。本研究可能有助于最大限度减少神经科医生在试图对这些疾病进行早期分类时遇到的困难。