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阿尔茨海默病的生物标志物谱及脑脊液β-淀粉样肽和tau 水平之间关联的动态变化。

Biomarker profiles of Alzheimer's disease and dynamic of the association between cerebrospinal fluid levels of β-amyloid peptide and tau.

机构信息

Cognitive Neurology Center, Saint Louis-Lariboisiere-Fernand Widal Hospital, AP-HP, Université de Paris, Paris, France.

Inserm U1153, CRESS, Epidemiology of Ageing and Neurodegenerative diseases, Université de Paris, Paris, France.

出版信息

PLoS One. 2019 May 14;14(5):e0217026. doi: 10.1371/journal.pone.0217026. eCollection 2019.

Abstract

OBJECTIVE

To investigate the relationship between cerebrospinal fluid (CSF) β-amyloid peptide (Aβ42) and CSF Tau in a large population of patients referred to memory clinics for investigation of cognitive dysfunction.

METHODS

We analyzed Alzheimer's disease (AD) biomarkers in CSF taken from 3565 patients referred to 18 French memory clinics. Patients were classified into four profiles according to levels of CSF biomarkers (A: amyloidosis, N: neurodegeneration). The association between CSF Tau and CSF Aβ42 were analyzed using general linear regression models, in the overall population and stratified by biomarkers profiles. We compared linear and quadratic models using Akaike information criterion. We also assessed change in biomarker profiles in a subset of patients who had 2 assessments of biomarkers.

RESULTS

CSF Tau was negatively associated with CSF Aβ42 in the overall population, following a non-linear quadratic model. However, the nature of this association was different in the 4 profiles: positive association in A-N- profile, negative association in A-N+ and A+N+ profiles, lack of association in A+N- patients. When considering patients with longitudinal data on profiles, 36% of those initially classified as A-N+ evolved to an A+N+ profile.

CONCLUSIONS

The nature of the association between CSF Aβ42 and CFS Tau depends on the A/N profiles of patients. These results suggest an increase in CSF Aβ42 early in the disease before its decline while tau pathology progresses, this pattern is particularly observed in non-APOE4 subjects. This phenomenon may explain why some patients with neurodegeneration only markers convert to an AD profile (A+N+) over time.

摘要

目的

在大量因认知功能障碍而被转介至记忆门诊的患者中,研究脑脊液(CSF)β-淀粉样蛋白肽(Aβ42)与 CSF Tau 之间的关系。

方法

我们分析了来自 18 家法国记忆诊所的 3565 名患者的 CSF 阿尔茨海默病(AD)生物标志物。根据 CSF 生物标志物水平(A:淀粉样变性,N:神经退行性变),将患者分为 4 种类型。采用一般线性回归模型,在总体人群中和根据生物标志物类型分层的情况下,分析 CSF Tau 与 CSF Aβ42 之间的关系。我们使用赤池信息量准则比较线性和二次模型。我们还在一部分具有 2 次生物标志物评估的患者亚组中评估了生物标志物类型的变化。

结果

在总体人群中,CSF Tau 与 CSF Aβ42 呈负相关,符合非线性二次模型。然而,这种相关性在 4 种类型中的性质不同:在 A-N-类型中呈正相关,在 A-N+和 A+N+类型中呈负相关,在 A+N-患者中无相关性。当考虑具有生物标志物类型纵向数据的患者时,最初被分类为 A-N+的患者中有 36%演变为 A+N+类型。

结论

CSF Aβ42 与 CSF Tau 之间的相关性取决于患者的 A/N 类型。这些结果表明,在 Tau 病理学进展的同时,疾病早期 CSF Aβ42 会增加,然后下降,这种模式在非 APOE4 患者中尤为明显。这种现象可能解释了为什么一些只有神经退行性变标志物的患者随着时间的推移会转化为 AD 类型(A+N+)。

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