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Phosphorylated Tau 181 Serum Levels Predict Alzheimer’s Disease in the Preclinical Stage

BACKGROUND: There is an urgent need for cost-effective, easy-to-measure biomarkers to identify subjects who will develop Alzheimer’s disease (AD), especially at the pre-symptomatic stage. This stage can be determined in autosomal dominant AD (ADAD) which offers the opportunity to observe the dynamic...

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Autores principales: Qin, Wei, Li, Fangyu, Jia, Longfei, Wang, Qi, Li, Ying, Wei, Yiping, Li, Yan, Jin, Hongmei, Jia, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234327/
https://www.ncbi.nlm.nih.gov/pubmed/35769604
http://dx.doi.org/10.3389/fnagi.2022.900773
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author Qin, Wei
Li, Fangyu
Jia, Longfei
Wang, Qi
Li, Ying
Wei, Yiping
Li, Yan
Jin, Hongmei
Jia, Jianping
author_facet Qin, Wei
Li, Fangyu
Jia, Longfei
Wang, Qi
Li, Ying
Wei, Yiping
Li, Yan
Jin, Hongmei
Jia, Jianping
author_sort Qin, Wei
collection PubMed
description BACKGROUND: There is an urgent need for cost-effective, easy-to-measure biomarkers to identify subjects who will develop Alzheimer’s disease (AD), especially at the pre-symptomatic stage. This stage can be determined in autosomal dominant AD (ADAD) which offers the opportunity to observe the dynamic biomarker changes during the life-course of AD stages. This study aimed to investigate serum biomarkers during different AD stages and potential novel protein biomarkers of presymptomatic AD. METHODS: In the first stage, 32 individuals [20 mutation carriers including 10 with AD, and 10 with mild cognitive impairment (MCI), and 12 healthy controls] from ADAD families were analyzed. All subjects underwent a complete clinical evaluation and a comprehensive neuropsychological battery. Serum samples were collected from all subjects, and antibody arrays were used to analyze 170 proteins in these samples. The most promising biomarkers were identified during this screening and were then measured in serum samples of 12 subjects with pre-MCI and 20 controls. RESULTS: The serum levels of 13 proteins were significantly different in patients with AD or MCI compared to controls. Of the 13 proteins, cathepsin D, immunoglobulin E, epidermal growth factor receptor (EGFR), matrix metalloproteinase-9 (MMP-9), von Willebrand factor (vWF), haptoglobin, and phosphorylated Tau-181 (p-Tau181) correlated with all cognitive measures (R(2) = −0.69–0.76). The areas under the receiver operating characteristic curve of these seven proteins were 0.71–0.93 for the classification of AD and 0.57–0.95 for the classification of MCI. Higher levels of p-Tau181 were found in the serum of pre-MCI subjects than in the serum of controls. The p-Tau181 serum level might detect AD before symptoms occur (area under the curve 0.85, sensitivity 75%, specificity 81.67%). CONCLUSIONS: A total of 13 serum proteins showed significant differences between subjects with AD and MCI and healthy controls. The p-Tau181 serum level might be a broadly available and cost-effective biomarker to identify individuals with preclinical AD and assess the severity of AD.
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spelling pubmed-92343272022-06-28 Phosphorylated Tau 181 Serum Levels Predict Alzheimer’s Disease in the Preclinical Stage Qin, Wei Li, Fangyu Jia, Longfei Wang, Qi Li, Ying Wei, Yiping Li, Yan Jin, Hongmei Jia, Jianping Front Aging Neurosci Aging Neuroscience BACKGROUND: There is an urgent need for cost-effective, easy-to-measure biomarkers to identify subjects who will develop Alzheimer’s disease (AD), especially at the pre-symptomatic stage. This stage can be determined in autosomal dominant AD (ADAD) which offers the opportunity to observe the dynamic biomarker changes during the life-course of AD stages. This study aimed to investigate serum biomarkers during different AD stages and potential novel protein biomarkers of presymptomatic AD. METHODS: In the first stage, 32 individuals [20 mutation carriers including 10 with AD, and 10 with mild cognitive impairment (MCI), and 12 healthy controls] from ADAD families were analyzed. All subjects underwent a complete clinical evaluation and a comprehensive neuropsychological battery. Serum samples were collected from all subjects, and antibody arrays were used to analyze 170 proteins in these samples. The most promising biomarkers were identified during this screening and were then measured in serum samples of 12 subjects with pre-MCI and 20 controls. RESULTS: The serum levels of 13 proteins were significantly different in patients with AD or MCI compared to controls. Of the 13 proteins, cathepsin D, immunoglobulin E, epidermal growth factor receptor (EGFR), matrix metalloproteinase-9 (MMP-9), von Willebrand factor (vWF), haptoglobin, and phosphorylated Tau-181 (p-Tau181) correlated with all cognitive measures (R(2) = −0.69–0.76). The areas under the receiver operating characteristic curve of these seven proteins were 0.71–0.93 for the classification of AD and 0.57–0.95 for the classification of MCI. Higher levels of p-Tau181 were found in the serum of pre-MCI subjects than in the serum of controls. The p-Tau181 serum level might detect AD before symptoms occur (area under the curve 0.85, sensitivity 75%, specificity 81.67%). CONCLUSIONS: A total of 13 serum proteins showed significant differences between subjects with AD and MCI and healthy controls. The p-Tau181 serum level might be a broadly available and cost-effective biomarker to identify individuals with preclinical AD and assess the severity of AD. Frontiers Media S.A. 2022-06-13 /pmc/articles/PMC9234327/ /pubmed/35769604 http://dx.doi.org/10.3389/fnagi.2022.900773 Text en Copyright © 2022 Qin, Li, Jia, Wang, Li, Wei, Li, Jin and Jia. 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
Qin, Wei
Li, Fangyu
Jia, Longfei
Wang, Qi
Li, Ying
Wei, Yiping
Li, Yan
Jin, Hongmei
Jia, Jianping
Phosphorylated Tau 181 Serum Levels Predict Alzheimer’s Disease in the Preclinical Stage
title Phosphorylated Tau 181 Serum Levels Predict Alzheimer’s Disease in the Preclinical Stage
title_full Phosphorylated Tau 181 Serum Levels Predict Alzheimer’s Disease in the Preclinical Stage
title_fullStr Phosphorylated Tau 181 Serum Levels Predict Alzheimer’s Disease in the Preclinical Stage
title_full_unstemmed Phosphorylated Tau 181 Serum Levels Predict Alzheimer’s Disease in the Preclinical Stage
title_short Phosphorylated Tau 181 Serum Levels Predict Alzheimer’s Disease in the Preclinical Stage
title_sort phosphorylated tau 181 serum levels predict alzheimer’s disease in the preclinical stage
topic Aging Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234327/
https://www.ncbi.nlm.nih.gov/pubmed/35769604
http://dx.doi.org/10.3389/fnagi.2022.900773
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