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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。

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.

机构信息

Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden.

Department of Neurology, Skåne University Hospital, Malmö, Sweden.

出版信息

Alzheimers Res Ther. 2020 Mar 24;12(1):30. doi: 10.1186/s13195-020-00592-8.

DOI:10.1186/s13195-020-00592-8
PMID:32209137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7093968/
Abstract

BACKGROUND

As research in treatments for neurocognitive diseases progresses, there is an increasing need to identify cognitive decline in the earliest stages of disease for initiation of treatment in addition to determining the efficacy of treatment. For early identification, accurate cognitive tests cutoff values for cognitive impairment are essential.

METHODS

We conducted a study on 297 cognitively healthy elderly people from the BioFINDER study and created subgroups excluding people with signs of underlying neuropathology, i.e., abnormal cerebrospinal fluid [CSF] β-amyloid or phosphorylated tau, CSF neurofilament light (neurodegeneration), or cerebrovascular pathology. We compared cognitive test results between groups and examined the age effect on cognitive test results.

RESULTS

In our subcohort without any measurable pathology (n = 120), participants achieved better test scores and significantly stricter cutoffs for cognitive impairment for almost all the examined tests. The age effect in this subcohort disappeared for all cognitive tests, apart from some attention/executive tests, predominantly explained by the exclusion of cerebrovascular pathology.

CONCLUSION

Our study illustrates a new approach to establish normative data that could be useful to identify earlier cognitive changes in preclinical dementias. Future studies need to investigate if there is a genuine effect of healthy aging on cognitive tests or if this age effect is a proxy for higher prevalence of preclinical neurodegenerative diseases.

摘要

背景

随着神经认知疾病治疗研究的进展,除了确定治疗效果外,越来越需要在疾病的早期阶段识别认知能力下降,以便开始治疗。为了早期识别,准确的认知测试对于认知障碍的截断值是必不可少的。

方法

我们对来自 BioFINDER 研究的 297 名认知健康的老年人进行了一项研究,并创建了排除有潜在神经病理学迹象的亚组,即异常脑脊液(CSF)β-淀粉样蛋白或磷酸化 tau、CSF 神经丝轻链(神经退行性变)或脑血管病理学。我们比较了不同组的认知测试结果,并检查了年龄对认知测试结果的影响。

结果

在我们没有任何可测量病理学的亚组中(n=120),参与者在几乎所有检查的测试中都取得了更好的测试分数和更严格的认知障碍截断值。除了一些注意力/执行测试外,这个亚组的年龄效应在所有认知测试中都消失了,这主要是由于排除了脑血管病理学。

结论

我们的研究说明了一种建立规范数据的新方法,这可能有助于识别前驱痴呆症中的早期认知变化。未来的研究需要调查认知测试中健康衰老是否有真正的影响,或者这种年龄效应是否是潜在神经退行性疾病更高患病率的替代指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54be/7093968/a0c148720912/13195_2020_592_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54be/7093968/a0c148720912/13195_2020_592_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54be/7093968/a0c148720912/13195_2020_592_Fig1_HTML.jpg

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Nat Med. 2020 Mar;26(3):379-386. doi: 10.1038/s41591-020-0755-1. Epub 2020 Mar 2.
2
Predicting clinical decline and conversion to Alzheimer's disease or dementia using novel Elecsys Aβ(1-42), pTau and tTau CSF immunoassays.使用新型 Elecsys Aβ(1-42)、pTau 和 tTau 脑脊液免疫分析物预测临床衰退和向阿尔茨海默病或痴呆的转化。
Sci Rep. 2019 Dec 13;9(1):19024. doi: 10.1038/s41598-019-54204-z.
3
梅奥正常标准研究:听觉词语学习测验的淀粉样蛋白和神经退行性变阴性正常标准数据,以及对轻度认知障碍/痴呆的性别特异性敏感性。
J Alzheimers Dis. 2024;100(3):879-897. doi: 10.3233/JAD-240081.
4
Defining exceptional cognition in older adults: A systematic review of cognitive super-ageing.定义老年人的非凡认知:认知超级老龄化的系统综述。
Int J Geriatr Psychiatry. 2023 Dec;38(12):e6034. doi: 10.1002/gps.6034.
5
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Clin Neuropsychol. 2024 Jul;38(5):1227-1255. doi: 10.1080/13854046.2023.2276967. Epub 2023 Nov 16.
6
Effects of Brain Pathologies on Spatiotemporal Gait Parameters in Patients with Mild Cognitive Impairment.脑病理变化对轻度认知障碍患者时空步态参数的影响。
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8
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10
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7
Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer's disease.血清神经丝动态预测无症状阿尔茨海默病的神经退行性变和临床进展。
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8
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9
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