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两种分析平台在脑脊液生物标志物用于阿尔茨海默病谱系与淀粉样蛋白PET成像分类中的比较

Comparison of Two Analytical Platforms in Cerebrospinal Fluid Biomarkers for the Classification of Alzheimer's Disease Spectrum with Amyloid PET Imaging.

作者信息

Lim Ho Jae, Park Jung Eun, Kim Byeong C, Choi Seong-Min, Song Min-Kyung, Cho Soo Hyun, Seo Hyeon Jeong, Kim Jahae, Song Ho-Chun, Choi Kyu Yeong, Lee Jang Jae, Kim Hoo-Won, Ha Jung-Min, Song Woo Keun, Park Sung-Gyoo, Lee Jung Sup, Lee Kun Ho

机构信息

Department of Biomedical Science, Chosun University, Gwangju, Republic of Korea.

BK21-plus Research Team for Bioactive Control Technology, Chosun University, Gwangju, Republic of Korea.

出版信息

J Alzheimers Dis. 2020;75(3):949-958. doi: 10.3233/JAD-191331.

Abstract

BACKGROUND

Cerebrospinal fluid (CSF) amyloid-β1-42 (Aβ1-42), total tau protein (t-Tau), and phosphorylated Tau (p-Tau) are ATN biomarkers for Alzheimer's disease (AD) and reflect pathogenic changes in the brain. CSF biomarkers of AD are considered for inclusion in the diagnostic criteria for research and clinical purposes to reduce the uncertainty of clinical diagnosis and to distinguish among AD stages.

OBJECTIVE

This study aims to compare two commercially available analytical platforms with respect to accuracy and the potential for early diagnosis of AD.

METHODS

A total of 211 CSF samples from healthy control (HC) and AD subjects were analyzed using two analytical platforms, INNOTEST ELISA and INNOBIA AlzBio3 xMAP kits. The accuracy of diagnosis and AUC values distinguishing study groups were compared between the two analytical platforms.

RESULTS

The absolute values for Aβ1-42, t-Tau, and p-Tau181 levels differed between the two platforms. The Aβ1-42 levels decreased, while t-Tau and p-Tau levels increased according to the AD stages. The AUC of Aβ1-42 and t-Tau, which distinguish the early stages of AD (preclinical and prodromal AD), were similar between the two platforms, whereas there were significant differences in p-Tau AUC values. CSF p-Tau using the INNOBIA was highly accurate for distinguishing both preclinical AD (AUC = 0.826, cut-off score≥38.89) and prodromal AD (AUC = 0.862, cut-off score≥41.88) from HC.

CONCLUSION

The accuracy of CSF p-Tau levels in the preclinical and prodromal AD is higher for the INNOBIA than the INNOTEST, and the early stage AD can be accurately distinguished from HC.

摘要

背景

脑脊液(CSF)淀粉样β蛋白1-42(Aβ1-42)、总tau蛋白(t-Tau)和磷酸化tau蛋白(p-Tau)是阿尔茨海默病(AD)的ATN生物标志物,反映大脑中的致病变化。AD的脑脊液生物标志物被考虑纳入研究和临床诊断标准,以减少临床诊断的不确定性,并区分AD的不同阶段。

目的

本研究旨在比较两种商用分析平台在AD诊断准确性和早期诊断潜力方面的差异。

方法

使用两种分析平台,即INNOTEST ELISA和INNOBIA AlzBio3 xMAP试剂盒,对来自健康对照(HC)和AD患者的211份脑脊液样本进行分析。比较两种分析平台在区分研究组时的诊断准确性和AUC值。

结果

两种平台的Aβ1-42、t-Tau和p-Tau181水平的绝对值不同。根据AD阶段,Aβ1-42水平降低,而t-Tau和p-Tau水平升高。两种平台区分AD早期阶段(临床前和前驱期AD)的Aβ1-42和t-Tau的AUC相似,而p-Tau的AUC值存在显著差异。使用INNOBIA检测的脑脊液p-Tau在区分临床前AD(AUC = 0.826,临界值≥38.89)和前驱期AD(AUC = 0.862,临界值≥41.88)与HC方面具有较高的准确性。

结论

INNOBIA检测脑脊液p-Tau水平在临床前和前驱期AD的准确性高于INNOTEST,并且可以准确地将早期AD与HC区分开来。

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