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帕金森病中轻度认知障碍的发病

Onset of Mild Cognitive Impairment in Parkinson Disease.

作者信息

Johnson David K, Langford Zachary, Garnier-Villarreal Mauricio, Morris John C, Galvin James E

机构信息

*Department of Psychology†Alzheimer Disease Center, University of Kansas‡Departments of Neurology, Pathology and Immunology, Alzheimer Disease Research Center, Washington University, St Louis§Departments of Neurology, Psychiatry, and Population Health, Center for Cognitive Neurology, New York University School of Medicine.

出版信息

Alzheimer Dis Assoc Disord. 2016 Apr-Jun;30(2):127-33. doi: 10.1097/WAD.0000000000000088.

Abstract

OBJECTIVE

Characterize the onset and timing of cognitive decline in Parkinson disease (PD) from the first recognizable stage of cognitively symptomatic PD-mild cognitive impairment (PD-MCI) to PD dementia (PDD). Thirty-nine participants progressed from PD to PDD and 25 remained cognitively normal.

METHODS

Bayesian-estimated disease-state models described the onset of an individual's cognitive decline across 12 subtests with a change point.

RESULTS

Subtests measuring working memory, visuospatial processing ability, and crystalized memory changed significantly 3 to 5 years before their first nonzero Clinical Dementia Rating and progressively worsened from PD to PD-MCI to PDD. Crystalized memory deficits were the hallmark feature of imminent conversion of cognitive status. Episodic memory tasks were not sensitive to onset of PD-MCI. For cognitively intact PD, all 12 subtests showed modest linear decline without evidence of a change point.

CONCLUSIONS

Longitudinal disease-state models support a prodromal dementia stage (PD-MCI) marked by early declines in working memory and visuospatial processing beginning 5 years before clinical diagnosis of PDD. Cognitive declines in PD affect motor ability (bradykinesia), working memory, and processing speed (bradyphrenia) resulting in PD-MCI where visuospatial imagery and memory retrieval deficits manifest before eventual development of overt dementia. Tests of episodic memory may not be sufficient to detect and quantify cognitive decline in PD.

摘要

目的

描述帕金森病(PD)从认知症状性PD-轻度认知障碍(PD-MCI)的首个可识别阶段到PD痴呆(PDD)的认知衰退的起始和时间。39名参与者从PD进展为PDD,25名认知保持正常。

方法

贝叶斯估计的疾病状态模型描述了个体在12个有变化点的子测试中的认知衰退起始情况。

结果

测量工作记忆、视觉空间处理能力和晶态记忆的子测试在其首个非零临床痴呆评定前3至5年出现显著变化,并从PD到PD-MCI再到PDD逐渐恶化。晶态记忆缺陷是认知状态即将转变的标志性特征。情景记忆任务对PD-MCI的起始不敏感。对于认知完好的PD患者,所有12个子测试均显示出适度的线性下降,无变化点证据。

结论

纵向疾病状态模型支持一个前驱性痴呆阶段(PD-MCI),其特征为在PDD临床诊断前5年开始工作记忆和视觉空间处理能力早期下降。PD的认知衰退会影响运动能力(运动迟缓)、工作记忆和处理速度(思维迟缓),导致PD-MCI,其中视觉空间意象和记忆检索缺陷在明显痴呆最终发展之前就已显现。情景记忆测试可能不足以检测和量化PD的认知衰退。

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