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J Neuropsychol. 2023 Mar;17(1):108-124. doi: 10.1111/jnp.12289. Epub 2022 Sep 19.
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Neurology. 2022 Apr 12;98(15):e1525-e1533. doi: 10.1212/WNL.0000000000013299. Epub 2022 Jan 12.
3
Enhancing the Sensitivity of Memory Tests: Reference Data for the Free and Cued Selective Reminding Test and the Logical Memory Task from Cognitively Healthy Subjects with Normal Alzheimer's Disease Cerebrospinal Fluid Biomarker Levels.提高记忆测试的灵敏度:认知健康且阿尔茨海默病脑脊液生物标志物水平正常的被试在自由和线索选择性提醒测试及逻辑记忆任务中的参考数据。
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4
Undetected Neurodegenerative Disease Biases Estimates of Cognitive Change in Older Adults.未被发现的神经退行性疾病会影响老年人认知变化的评估。
Psychol Sci. 2021 Jun;32(6):849-860. doi: 10.1177/0956797620985518. Epub 2021 May 27.
5
Estimating prevalence of subjective cognitive decline in and across international cohort studies of aging: a COSMIC study.估算老龄化国际队列研究中及跨队列研究中主观认知衰退的患病率:一项 COSMIC 研究。
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The A4 study: β-amyloid and cognition in 4432 cognitively unimpaired adults.A4 研究:4432 名认知正常成年人中的β-淀粉样蛋白与认知。
Ann Clin Transl Neurol. 2020 May;7(5):776-785. doi: 10.1002/acn3.51048. Epub 2020 Apr 21.
8
The age-related effect on cognitive performance in cognitively healthy elderly is mainly caused by underlying AD pathology or cerebrovascular lesions: implications for cutoffs regarding cognitive impairment.认知健康老年人认知表现的年龄相关影响主要是由潜在的 AD 病理学或脑血管病变引起的:对认知障碍相关截断值的影响。
Alzheimers Res Ther. 2020 Mar 24;12(1):30. doi: 10.1186/s13195-020-00592-8.
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The characterisation of subjective cognitive decline.主观认知下降的特征。
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Sex-specific norms for verbal memory tests may improve diagnostic accuracy of amnestic MCI.记忆障碍型轻度认知障碍的诊断准确性可能因使用语言记忆测试的性别特异性常模而提高。
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认知健康且阿尔茨海默病脑脊液生物标志物水平正常个体的注意力、执行功能、语言和视觉处理测试的参考数据。

Reference Data for Attentional, Executive, Linguistic, and Visual Processing Tests Obtained from Cognitively Healthy Individuals with Normal Alzheimer's Disease Cerebrospinal Fluid Biomarker Levels.

机构信息

Barcelonaβeta Brain Research Center (BBRC), Pasqual Maragall Foundation, Barcelona, Spain.

Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.

出版信息

J Alzheimers Dis. 2023;95(1):237-249. doi: 10.3233/JAD-230290.

DOI:10.3233/JAD-230290
PMID:37483000
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10578268/
Abstract

BACKGROUND

Conventional neuropsychological norms likely include cognitively unimpaired (CU) individuals with preclinical Alzheimer's disease (AD) pathology (amyloid-β, tau, and neurodegeneration) since they are based on cohorts without AD biomarkers data. Due to this limitation, population-based norms would lack sensitivity for detecting subtle cognitive decline due to AD, the transitional stage between healthy cognition and mild cognitive impairment. We have recently published norms for memory tests in individuals with normal cerebrospinal fluid (CSF) AD biomarker levels.

OBJECTIVE

The aim of the present study was to provide further AD biomarker-based cognitive references covering attentional, executive function, linguistic, and visual processing tests.

METHODS

We analyzed 248 CU individuals aged between 50-70 years old with normal CSF Aβ, p-tau, and neurodegeneration (t-tau) biomarker levels. The tests included were the Trail Making Test (TMT), Semantic Fluency Test, Digit and Symbol Span, Coding, Matrix Reasoning, Judgement of Line Orientation and Visual Puzzles. Normative data were developed based on regression models adjusted for age, education, and sex when needed. We present equations to calculate z-scores, the corresponding normative percentile tables, and online calculators.

RESULTS

Age, education, and sex were associated with performance in all tests, except education for the TMT-A, and sex for the TMT-B, Coding, and Semantic Fluency. Cut-offs derived from the current biomarker-based reference data were higher and more sensitive than standard norms.

CONCLUSION

We developed reference data obtained from individuals with evidence of non-pathologic AD biomarker levels that may improve the objective characterization of subtle cognitive decline in preclinical AD.

摘要

背景

传统的神经心理学标准可能包括认知未受损(CU)的个体,这些个体有临床前阿尔茨海默病(AD)病理学(淀粉样蛋白-β、tau 和神经退行性变),因为它们是基于没有 AD 生物标志物数据的队列。由于这一限制,基于人群的标准将缺乏对 AD 导致的轻微认知衰退的敏感性,AD 是健康认知和轻度认知障碍之间的过渡阶段。我们最近发表了脑脊液(CSF)AD 生物标志物水平正常的个体记忆测试的标准。

目的

本研究的目的是提供进一步的基于 AD 生物标志物的认知参考,涵盖注意力、执行功能、语言和视觉处理测试。

方法

我们分析了 248 名年龄在 50-70 岁之间的 CU 个体,他们的 CSF Aβ、p-tau 和神经退行性变(t-tau)生物标志物水平正常。包括的测试有连线测试(TMT)、语义流畅性测试、数字和符号跨度、编码、矩阵推理、线定向判断和视觉拼图。当需要时,根据回归模型调整年龄、教育和性别进行了规范数据的开发。我们提供了计算 z 分数的方程、相应的规范百分位表和在线计算器。

结果

除了 TMT-A 与教育相关,TMT-B、编码和语义流畅性与性别相关外,所有测试的年龄、教育和性别都与表现相关。从当前基于生物标志物的参考数据得出的截止值更高,更敏感。

结论

我们开发了从具有非病理 AD 生物标志物水平证据的个体获得的参考数据,这可能有助于客观描述临床前 AD 中的轻微认知衰退。