Department of Neurology, McGill University, Montreal General Hospital, Montreal, QC H3G 1A4, Canada.
Brain. 2012 Jun;135(Pt 6):1860-70. doi: 10.1093/brain/aws093. Epub 2012 May 4.
Parkinsonism, as a gradually progressive disorder, has a prodromal interval during which neurodegeneration has begun but cardinal manifestations have not fully developed. A systematic direct assessment of this interval has never been performed. Since patients with idiopathic REM sleep behaviour disorder are at very high risk of parkinsonism, they provide a unique opportunity to observe directly the development of parkinsonism. Patients with idiopathic REM sleep behaviour disorder in an ongoing cohort study were evaluated annually with several quantitative motor measures, including the Unified Parkinson's Disease Rating Scale, Purdue Pegboard, alternate-tap test and timed up-and-go. Patients who developed parkinsonism were identified from this cohort and matched according to age to normal controls. Their results on motor testing from the preceding years were plotted, and then assessed with regression analysis, to determine when markers first deviated from normal values. Sensitivity and specificity of quantitative motor markers for diagnosing prodromal parkinsonism were assessed. Of 78 patients, 20 developed parkinsonism. On regression analysis, the Unified Parkinson's Disease Rating Scale first intersected normal values at an estimated 4.5 years before diagnosis. Voice and face akinesia intersected earliest (estimated prodromal interval = 9.8 years), followed by rigidity (4.4 years), gait abnormalities (4.4 years) and limb bradykinesia (4.2 years). Quantitative motor tests intersected normal values at longer prodromal intervals than subjective examination (Purdue Pegboard = 8.6 years, alternate-tap = 8.2, timed up-and-go = 6.3). Using Purdue Pegboard and the alternate-tap test, parkinsonism could be detected with 71-82% sensitivity and specificity 3 years before diagnosis, whereas a Unified Parkinson's Disease Rating Scale score >4 identified prodromal parkinsonism with 88% sensitivity and 94% specificity 2 years before diagnosis. Removal of action tremor scores improved sensitivity to 94% and specificity to 97% at 2 years before diagnosis (cut-off >3). Although distinction between conditions was often difficult, prodromal dementia with Lewy bodies appeared to have a slower progression than Parkinson's disease (prodromal interval = 6.0 versus 3.8 years). Using a cut-off of Unified Parkinson's Disease Rating Scale >3 (excluding action tremor), 25% of patients with 'still-idiopathic' REM sleep behaviour disorder demonstrated evidence of possible prodromal parkinsonism. Therefore, using direct assessment of motor examination before parkinsonism in a REM sleep behaviour disorder, we have estimated a prodromal interval of ∼4.5 years on the Unified Parkinson's Disease Rating Scale; other quantitative markers may detect parkinsonism earlier. Simple quantitative motor measures may be capable of reliably detecting parkinsonism, even before a clinical diagnosis can be made by experienced movement disorders neurologists.
帕金森病是一种逐渐进展的疾病,在神经退行性变开始但主要表现尚未完全发展的前驱期有一个潜伏期。目前尚未对这一潜伏期进行系统的直接评估。由于特发性 REM 睡眠行为障碍患者发生帕金森病的风险极高,因此他们为直接观察帕金森病的发展提供了独特的机会。在一项正在进行的队列研究中,对特发性 REM 睡眠行为障碍患者进行了每年一次的多项定量运动评估,包括统一帕金森病评定量表、Purdue 钉板、交替敲击测试和起立-行走计时测试。从该队列中确定了发生帕金森病的患者,并根据年龄与正常对照进行匹配。分析他们之前年度的运动测试结果,并通过回归分析确定标记物何时首次偏离正常值。评估定量运动标志物对诊断前驱期帕金森病的敏感性和特异性。在 78 名患者中,有 20 名发展为帕金森病。在回归分析中,统一帕金森病评定量表估计在诊断前 4.5 年前首次与正常值相交。声音和面部运动迟缓最早相交(估计前驱期间隔= 9.8 年),其次是僵硬(4.4 年)、步态异常(4.4 年)和肢体运动迟缓(4.2 年)。定量运动测试的前驱期间隔长于主观检查(Purdue 钉板= 8.6 年,交替敲击= 8.2 年,起立-行走计时测试= 6.3 年)。使用 Purdue 钉板和交替敲击测试,帕金森病可在诊断前 3 年以 71-82%的敏感性和特异性 71-82%检测到,而统一帕金森病评定量表评分>4 在诊断前 2 年以 88%的敏感性和 94%的特异性识别前驱期帕金森病。在诊断前 2 年,去除动作震颤评分可将敏感性提高至 94%,特异性提高至 97%(>3 为截断值)。尽管区分这些情况通常很困难,但路易体痴呆的前驱期似乎比帕金森病进展更慢(前驱期间隔= 6.0 年比 3.8 年)。使用统一帕金森病评定量表>3(不包括动作震颤)的截断值,25%的“仍为特发性” REM 睡眠行为障碍患者有前驱期帕金森病的证据。因此,通过 REM 睡眠行为障碍中运动检查的直接评估,我们在统一帕金森病评定量表上估计了大约 4.5 年的前驱期;其他定量标志物可能更早发现帕金森病。简单的定量运动测量可能能够可靠地检测帕金森病,甚至在经验丰富的运动障碍神经科医生做出临床诊断之前。