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血浆焦谷氨酸修饰的β淀粉样蛋白可区分淀粉样病变。

Plasma pyroglutamate-modified amyloid beta differentiates amyloid pathology.

作者信息

Wang Pei-Ning, Lin Kun-Ju, Liu Huei-Chun, Andreasson Ulf, Blennow Kaj, Zetterberg Henrik, Yang Shieh-Yueh

机构信息

Department of Neurology Neurological Institute Taipei Veterans General Hospital Taipei Taiwan.

Department of Neurology School of Medicine National Yang-Ming University Taipei Taiwan.

出版信息

Alzheimers Dement (Amst). 2020 Apr 30;12(1):e12029. doi: 10.1002/dad2.12029. eCollection 2020.

DOI:10.1002/dad2.12029
PMID:32363230
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7191392/
Abstract

INTRODUCTION

Pyroglutamate-modified amyloid β (Aβ) could be a biomarker for Aβ plaque pathology in the brain. An ultra-high-sensitive assay is needed for detecting Aβ.

METHODS

Immunomagnetic reduction was used for quantification of Aβ in plasma from 46 participants. The concentrations of Aβ of these subjects were compared with F-florbetapir positron emission tomography (PET) images.

RESULTS

Aβ concentration was 44.1 ± 28.2 fg/mL in PET- (n = 28) and 91.6 ± 54.6 fg/mL in PET+ (n = 18; < .05). The cutoff value of Aβ for discriminating PET- from PET+ was 55.5 fg/mL, resulting in a sensitivity of 83.3%, a specificity of 71.4%. The concentration of Aβ showed a moderate correlation (r = 0.437) with PET standardized uptake value ratio.

DISCUSSION

We did not enroll pre-clinical AD subject with normal cognition but Aβ PET+. It would be an important issue to explore the feasibility of using Aβ for screening pre-clinical subjects.

CONCLUSION

These results reveal the feasibility of detecting Aβ pathology using quantification of a plaque-derived Aβ molecule in plasma.

摘要

引言

焦谷氨酸修饰的淀粉样β蛋白(Aβ)可能是大脑中Aβ斑块病理学的生物标志物。检测Aβ需要一种超高灵敏度的检测方法。

方法

采用免疫磁珠法对46名参与者血浆中的Aβ进行定量。将这些受试者的Aβ浓度与F-氟代苯并噻唑正电子发射断层扫描(PET)图像进行比较。

结果

PET-组(n = 28)的Aβ浓度为44.1±28.2 fg/mL,PET+组(n = 18;P <.05)为91.6±54.6 fg/mL。区分PET-和PET+的Aβ临界值为55.5 fg/mL,灵敏度为83.3%,特异性为71.4%。Aβ浓度与PET标准化摄取值比值呈中度相关(r = 0.437)。

讨论

我们未纳入认知正常但Aβ PET+的临床前AD受试者。探索使用Aβ筛查临床前受试者的可行性将是一个重要问题。

结论

这些结果揭示了通过定量血浆中斑块衍生的Aβ分子来检测Aβ病理学的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9219/7191392/3061955839ef/DAD2-12-e12029-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9219/7191392/4717821c9c8b/DAD2-12-e12029-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9219/7191392/1748c269d0b9/DAD2-12-e12029-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9219/7191392/3061955839ef/DAD2-12-e12029-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9219/7191392/4717821c9c8b/DAD2-12-e12029-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9219/7191392/1748c269d0b9/DAD2-12-e12029-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9219/7191392/3061955839ef/DAD2-12-e12029-g003.jpg

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