CWPT(颜色词挑选测试)可用于痴呆临床前阶段轻微障碍的分类

T. Shimura
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引用次数: 2

摘要

目的:在轻度认知障碍(MCI)和临床前痴呆(PCSD)概念出现之前,我们的研究开始检测到大脑的轻微衰退。本研究的目的是阐明设计的CWPT(颜色选词测试)在MCI和PCSD中检测轻微障碍并对其进行分类的能力基础。方法:CWPT是Stroop效应的一种应用,包括情景记忆的检查以获得证据,1使用推断谱法激活前额叶,2使用CWPT、WCST、HCL、FAB和MMSE进行标准相关效度测试,3使用MMSE和CWPT进行敏感性和特异性测试。结果:1利用近红外光谱分析发现,与快速重复4-5个顺序、倒序、川岛算术练习和KPT(取名测验)相比,CWPT是最有效的脑激活测试。2在22名健康老年人的直方图中,除了CWPT与WCST有良好的相关性外,只有CWPT与WCST呈正态分布。3使用MMSE作为真实条件和CWPT作为预测条件计算29例痴呆患者的敏感性和特异性。以CWPT平均1.5 sd为截点,灵敏度为0.963,特异性为1.0。结论:这些分析的结果表明,CWPT可用于MCI和痴呆临床前阶段的障碍水平分类。
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CWPT (Color Words Pick-Out Test) Available for Classifying the Slight Disorder on the Preclinical Stage of Dementia
Objective: Before concept of mild cognitive impairment (MCI) and preclinical stage of dementia (PCSD) our study started to detect slight declines in the brain. The purpose of this study is to clarify the basis of the ability of the devised CWPT (Color Word Pick-out Test) to detect slight disorder and classify it at the MCI and PCSD. Methods: CWPT is an application of Stroop effect and is including an examination of episodic memory to obtain the evidence and 1 activation of the prefrontal lobe using an inferred spectroscopy, 2 criterion-related validity using CWPT, WCST, HCL, FAB and MMSE 3 sensitivity and specificity using MMSE and CWPT are examined. Results: 1 It is found using a near infrared spectroscopy that CWPT is the most effective test for the brain activation, in comparison with quick repetition of 4-5numbers in order, in reverse order, Kawashima arithmetic drill and KPT (Kana Pick-out Test). 2 among the histograms obtained from 22 healthy aging people, only CWPT and WCST show normal distributions besides CWPT has good correlation with WCST. 3 Sensitivity and specificity are calculated using MMSE as a true condition and CWPT as a predicted condition for 29 subjects with dementia. Sensitivity becomes 0.963 and specificity becomes 1.0 by the cutoff of the average-1.5SD of CWPT. Conclusion: As a result of these analyses, it has been suggested that CWPT can be used to classify the level of disorder during MCI and the preclinical stage of dementia.
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