Normative Data of Mini-Mental State Examination, Montreal Cognitive Assessment, and Alzheimer's Disease Assessment Scale-Cognitive Subscale of Community-Dwelling Older Adults in Taiwan.

IF 2.2 4区 医学 Q3 CLINICAL NEUROLOGY Dementia and Geriatric Cognitive Disorders Pub Date : 2022-01-01 DOI:10.1159/000525615
Yi-Chia Wei, Chih-Ken Chen, Chemin Lin, Pin-Yuan Chen, Pei-Chun Hsu, Ching-Po Lin, Yu-Chiau Shyu, Wen-Yi Huang
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引用次数: 6

Abstract

Introduction: Appropriate tools and references are essential for evaluating individuals' cognitive levels. This study validated the Taiwan version of the Alzheimer's Disease Assessment Scale-Cognitive subscale (ADAS-cog) and provided normative data for the Mini-Mental State Examination (MMSE), the Montreal Cognitive Assessment (MoCA), and ADAS-cog in community-dwelling older adults.

Methods: MMSE, MoCA, and ADAS-cog were administered to 150 nondemented healthy adults aged 55-85 years during 2018-2020 as part of the Northeastern Taiwan Community Medicine Research Cohort. ADAS-cog was translated from the original English version to traditional Chinese with cultural and language considerations in Taiwan. Cronbach's alpha (α) tested the reliability of ADAS-cog, and Pearson correlations examined its external validity using MMSE and MoCA as comparisons. Normative data were generated and stratified by age and education, and the one-way analysis of variance compared scores between age and education groups. Another 20 hospital-acquired participants with cognitive impairment joined the 150 healthy participants. Comparisons in the Clinical Dementia Rating (CDR) tiers tested the discriminability of the tests for different cognitive levels. The area under the receiver operating characteristic curve (AUROC) analyzed the power of ADAS-cog in predicting CDR 0.5 from CDR 0.

Results: The Taiwan version of ADAS-cog had fair reliability between items (α = 0.727) and good correlations to MMSE (r = -0.673, p < 0.001) and MoCA (r = -0.746, p < 0.001). The normative data of MMSE, MoCA, and ADAS-cog showed ladder changes with age (p = 0.006, 0.001, and 0.437) and education (p < 0.001, <0.001, and <0.001) in the 150 nondemented older adults. Next, in the 170 mixed participants from the communities and the hospital, MMSE, MoCA, and ADAS-cog scores were well differentiable between CDR 0, 0.5, and 1. In addition, ADAS-cog discriminated CDR 0.5 from 0 by an AUROC of 0.827 (p < 0.001).

Discussion/conclusion: The three structured cognitive tests consistently reflect cognitive levels of healthy older adults. The Taiwan version of ADAS-cog is compatible with MMSE and MoCA to distinguish people with mildly impaired from normal cognition. In addition, this study derived MMSE, MoCA, and ADAS-cog norms tailored to demographic factors. The findings highlight the need for stratification of age and education rather than applying a fixed cutoff for defining normal and abnormal cognition.

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台湾社区居住老年人精神状态测验、蒙特娄认知评量与阿尔茨海默病评量量表-认知子量表之规范资料。
适当的工具和参考文献是评估个体认知水平的必要条件。本研究验证台湾版阿尔茨海默病评估量表-认知子量表(ADAS-cog),并为社区居住老年人的迷你精神状态检查(MMSE)、蒙特利尔认知评估(MoCA)和ADAS-cog提供规范性数据。方法:作为台湾东北社区医学研究队列的一部分,在2018-2020年期间,对150名55-85岁的无痴呆健康成人进行MMSE、MoCA和ADAS-cog治疗。考虑到台湾的文化和语言因素,ADAS-cog从原来的英文版本翻译成繁体中文。Cronbach’s alpha (α)检验ADAS-cog的信度,Pearson相关检验其外部效度,采用MMSE和MoCA作为比较。生成规范数据并按年龄和教育程度分层,并进行单向方差分析,比较年龄和教育程度组之间的得分。另外20名医院获得性认知障碍的参与者加入了150名健康参与者的行列。临床痴呆评分(CDR)等级的比较测试了不同认知水平测试的可辨别性。受试者工作特征曲线下面积(AUROC)分析了ADAS-cog从CDR 0预测CDR 0.5的能力。结果:台湾版ADAS-cog量表单项间具有较好的信度(α = 0.727),与MMSE (r = -0.673, p < 0.001)和MoCA (r = -0.746, p < 0.001)具有较好的相关性。MMSE、MoCA和ADAS-cog的规范性数据随年龄(p = 0.006、0.001和0.437)和教育程度(p < 0.001)呈阶梯变化。讨论/结论:三种结构化认知测试一致反映健康老年人的认知水平。台湾版ADAS-cog与MMSE及MoCA相容,可区分轻度认知障碍者与正常认知障碍者。此外,本研究还根据人口统计因素推导出MMSE、MoCA和ADAS-cog规范。研究结果强调了年龄和教育分层的必要性,而不是应用一个固定的界限来定义正常和异常的认知。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
46
审稿时长
2 months
期刊介绍: As a unique forum devoted exclusively to the study of cognitive dysfunction, ''Dementia and Geriatric Cognitive Disorders'' concentrates on Alzheimer’s and Parkinson’s disease, Huntington’s chorea and other neurodegenerative diseases. The journal draws from diverse related research disciplines such as psychogeriatrics, neuropsychology, clinical neurology, morphology, physiology, genetic molecular biology, pathology, biochemistry, immunology, pharmacology and pharmaceutics. Strong emphasis is placed on the publication of research findings from animal studies which are complemented by clinical and therapeutic experience to give an overall appreciation of the field.
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