GH Sergievsky Center, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
Mov Disord. 2010 Jan 30;25(2):172-8. doi: 10.1002/mds.22943.
There is some evidence that mild parkinsonian signs (MPSs) are associated with increased risk of dementia, suggesting that MPS could be an early biomarker for dementia. Our aims, in a new cohort, were to determine whether (1) baseline MPS are a predictor of incident dementia and (2) there is an interaction between MPS and other baseline risk factors for dementia (i.e., the presence of both together greatly elevates the risk of dementia) was the objective. In a prospective, longitudinal study of community-dwelling elders in northern Manhattan, NY, Parkinsonian signs were rated with an abbreviated Unified Parkinson's Disease Rating Scale. Risk of incident dementia was assessed using Cox proportional hazards models. There were 1,851 participants (mean follow-up = 3.7 years). Participants with baseline MPS were twice as likely to develop dementia as participants without MPS: 16.3% versus 7.7%, unadjusted hazards ratio (HR) = 2.24 (P< 0.001), adjusted HR = 1.98 (P < 0.001). MPS were divided into three subtypes: adjusted HR(axial dysfunction) = 2.45 (P < 0.001), adjusted HR(tremor) = 2.38 (P = 0.006), and adjusted HR(rigidity) = 1.16 (P = 0.58). When MPS were treated as a continuous variable, the adjusted HR = 1.15 (P = 0.001). There were no interactions between MPS and other baseline risk factors for dementia, including gender, education, race, family history of dementia, stroke, and apolipoprotein E-e4. Baseline MPS seems to be a predictor of incident dementia. These motor signs might, therefore, serve as a useful biomarker for emerging dementia.
有一些证据表明,轻度帕金森病体征(MPS)与痴呆风险增加有关,这表明 MPS 可能是痴呆的早期生物标志物。我们在一个新队列中的目标是确定:(1)基线 MPS 是否是痴呆事件的预测因素,(2)MPS 是否与痴呆的其他基线风险因素存在相互作用(即两者同时存在极大地增加了痴呆的风险)。在纽约州北部曼哈顿的一个社区居住的老年人的前瞻性、纵向研究中,使用简化的统一帕金森病评定量表(Unified Parkinson's Disease Rating Scale)评定帕金森病体征。使用 Cox 比例风险模型评估痴呆的发病风险。共有 1851 名参与者(平均随访时间=3.7 年)。基线时存在 MPS 的参与者发生痴呆的风险是没有 MPS 的参与者的两倍:16.3%比 7.7%,未调整的风险比(Hazard Ratio,HR)=2.24(P<0.001),调整后的 HR=1.98(P<0.001)。MPS 分为三种亚型:调整后的 HR(轴功能障碍)=2.45(P<0.001),调整后的 HR(震颤)=2.38(P=0.006),调整后的 HR(僵硬)=1.16(P=0.58)。当 MPS 作为连续变量处理时,调整后的 HR=1.15(P=0.001)。MPS 与痴呆的其他基线风险因素之间没有相互作用,包括性别、教育、种族、痴呆家族史、中风和载脂蛋白 E-e4。基线 MPS 似乎是痴呆事件的预测因素。因此,这些运动迹象可能是痴呆症早期的有用生物标志物。