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Plasma tau proteins for the diagnosis of mild cognitive impairment and Alzheimer's disease: A systematic review and meta-analysis

OBJECTIVE: Detecting plasma tau biomarkers used to be impossible due to their low concentrations in blood samples. Currently, new high-sensitivity assays made it a reality. We performed a systematic review and meta-analysis in order to test the accuracy of plasma tau protein in diagnosing Alzheimer&...

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Autores principales: Chen, Leian, Niu, Xiaoqian, Wang, Yuye, Lv, Shuang, Zhou, Xiao, Yang, Ziyuan, Peng, Dantao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358685/
https://www.ncbi.nlm.nih.gov/pubmed/35959295
http://dx.doi.org/10.3389/fnagi.2022.942629
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author Chen, Leian
Niu, Xiaoqian
Wang, Yuye
Lv, Shuang
Zhou, Xiao
Yang, Ziyuan
Peng, Dantao
author_facet Chen, Leian
Niu, Xiaoqian
Wang, Yuye
Lv, Shuang
Zhou, Xiao
Yang, Ziyuan
Peng, Dantao
author_sort Chen, Leian
collection PubMed
description OBJECTIVE: Detecting plasma tau biomarkers used to be impossible due to their low concentrations in blood samples. Currently, new high-sensitivity assays made it a reality. We performed a systematic review and meta-analysis in order to test the accuracy of plasma tau protein in diagnosing Alzheimer's disease (AD) or mild cognitive impairment (MCI). METHODS: We searched PubMed, Cochrane, Embase and Web of Science databases, and conducted correlation subgroup analysis, sensitivity analysis and publication bias analysis using R Programming Language. RESULTS: A total of 56 studies were included. Blood t-tau and p-tau levels increased from controls to MCI to AD patients, and showed significant changes in pairwise comparisons of AD, MCI and normal cognition. P-tau217 was more sensitive than p-tau181 and p-tau231 in different cognition periods. In addition, ultrasensitive analytical platforms, immunomagnetic reduction (IMR), increased the diagnostic value of tau proteins, especially the diagnostic value of t-tau. CONCLUSION: Both t-tau and p-tau are suitable AD blood biomarkers, and p-tau217 is more sensitive than other tau biomarkers to differentiate MCI and AD. Detection techniques also have an impact on biomarkers' results. New ultrasensitive analytical platforms of IMR increase the diagnostic value of both t-tau and p-tau biomarkers. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/PROSPERO/, registration number: CRD42021264701.
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spelling pubmed-93586852022-08-10 Plasma tau proteins for the diagnosis of mild cognitive impairment and Alzheimer's disease: A systematic review and meta-analysis Chen, Leian Niu, Xiaoqian Wang, Yuye Lv, Shuang Zhou, Xiao Yang, Ziyuan Peng, Dantao Front Aging Neurosci Aging Neuroscience OBJECTIVE: Detecting plasma tau biomarkers used to be impossible due to their low concentrations in blood samples. Currently, new high-sensitivity assays made it a reality. We performed a systematic review and meta-analysis in order to test the accuracy of plasma tau protein in diagnosing Alzheimer's disease (AD) or mild cognitive impairment (MCI). METHODS: We searched PubMed, Cochrane, Embase and Web of Science databases, and conducted correlation subgroup analysis, sensitivity analysis and publication bias analysis using R Programming Language. RESULTS: A total of 56 studies were included. Blood t-tau and p-tau levels increased from controls to MCI to AD patients, and showed significant changes in pairwise comparisons of AD, MCI and normal cognition. P-tau217 was more sensitive than p-tau181 and p-tau231 in different cognition periods. In addition, ultrasensitive analytical platforms, immunomagnetic reduction (IMR), increased the diagnostic value of tau proteins, especially the diagnostic value of t-tau. CONCLUSION: Both t-tau and p-tau are suitable AD blood biomarkers, and p-tau217 is more sensitive than other tau biomarkers to differentiate MCI and AD. Detection techniques also have an impact on biomarkers' results. New ultrasensitive analytical platforms of IMR increase the diagnostic value of both t-tau and p-tau biomarkers. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/PROSPERO/, registration number: CRD42021264701. Frontiers Media S.A. 2022-07-25 /pmc/articles/PMC9358685/ /pubmed/35959295 http://dx.doi.org/10.3389/fnagi.2022.942629 Text en Copyright © 2022 Chen, Niu, Wang, Lv, Zhou, Yang and Peng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Aging Neuroscience
Chen, Leian
Niu, Xiaoqian
Wang, Yuye
Lv, Shuang
Zhou, Xiao
Yang, Ziyuan
Peng, Dantao
Plasma tau proteins for the diagnosis of mild cognitive impairment and Alzheimer's disease: A systematic review and meta-analysis
title Plasma tau proteins for the diagnosis of mild cognitive impairment and Alzheimer's disease: A systematic review and meta-analysis
title_full Plasma tau proteins for the diagnosis of mild cognitive impairment and Alzheimer's disease: A systematic review and meta-analysis
title_fullStr Plasma tau proteins for the diagnosis of mild cognitive impairment and Alzheimer's disease: A systematic review and meta-analysis
title_full_unstemmed Plasma tau proteins for the diagnosis of mild cognitive impairment and Alzheimer's disease: A systematic review and meta-analysis
title_short Plasma tau proteins for the diagnosis of mild cognitive impairment and Alzheimer's disease: A systematic review and meta-analysis
title_sort plasma tau proteins for the diagnosis of mild cognitive impairment and alzheimer's disease: a systematic review and meta-analysis
topic Aging Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358685/
https://www.ncbi.nlm.nih.gov/pubmed/35959295
http://dx.doi.org/10.3389/fnagi.2022.942629
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