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Long-Term Storage Effects on Stability of Aβ(1–40), Aβ(1–42), and Total Tau Proteins in Human Plasma Samples Measured with Immunomagnetic Reduction Assays

BACKGROUND: The stability of Alzheimer's disease (AD) biomarkers in plasma, measured by immunomagnetic reduction (IMR) after long-term storage at −80°C, has not been established before. METHOD: Ninety-nine human plasma samples from 53 normal controls (NCs), 5 patients with amnestic mild cogniti...

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Autores principales: Chiu, Ming-Jang, Lue, Lih-Fen, Sabbagh, Marwan N., Chen, Ta-Fu, Chen, H.H., Yang, Shieh-Yueh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477481/
https://www.ncbi.nlm.nih.gov/pubmed/31043966
http://dx.doi.org/10.1159/000496099
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author Chiu, Ming-Jang
Lue, Lih-Fen
Sabbagh, Marwan N.
Chen, Ta-Fu
Chen, H.H.
Yang, Shieh-Yueh
author_facet Chiu, Ming-Jang
Lue, Lih-Fen
Sabbagh, Marwan N.
Chen, Ta-Fu
Chen, H.H.
Yang, Shieh-Yueh
author_sort Chiu, Ming-Jang
collection PubMed
description BACKGROUND: The stability of Alzheimer's disease (AD) biomarkers in plasma, measured by immunomagnetic reduction (IMR) after long-term storage at −80°C, has not been established before. METHOD: Ninety-nine human plasma samples from 53 normal controls (NCs), 5 patients with amnestic mild cognitive impairment (aMCI), and 41 AD patients were collected. Each plasma sample was aliquoted and stored as single-use aliquots at −80°C. The baseline measurements for Aβ(1–40), Aβ(1–42), and total Tau protein (T-Tau) concentrations for each sample were done within 3 months of blood draw by IMR. They are referred to as baseline concentrations. A separate aliquot from each sample was assayed with IMR to assess the stability of the measured analytes during storage at −80°C between 1.1 and 5.4 years. This is referred to as a repeated result. RESULTS: IMR shows that plasma levels of Aβ(1–40) and Aβ(1–42) exhibit stability over 5-year storage at −80°C and that plasma levels of T-Tau are less stable (approximately 1.5 years). CONCLUSION: Although the measured concentrations of T-Tau in human plasma may alter during storage, the diagnostic utility of the results are only slightly affected when the product of Aβ(1–42) and T-Tau concentrations are used. The results show that the overall agreement between baseline and repeated measurements in the ability of discriminating NCs from aMCI/AD patients is higher than 80%.
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spelling pubmed-64774812019-05-01 Long-Term Storage Effects on Stability of Aβ(1–40), Aβ(1–42), and Total Tau Proteins in Human Plasma Samples Measured with Immunomagnetic Reduction Assays Chiu, Ming-Jang Lue, Lih-Fen Sabbagh, Marwan N. Chen, Ta-Fu Chen, H.H. Yang, Shieh-Yueh Dement Geriatr Cogn Dis Extra Original Research Article BACKGROUND: The stability of Alzheimer's disease (AD) biomarkers in plasma, measured by immunomagnetic reduction (IMR) after long-term storage at −80°C, has not been established before. METHOD: Ninety-nine human plasma samples from 53 normal controls (NCs), 5 patients with amnestic mild cognitive impairment (aMCI), and 41 AD patients were collected. Each plasma sample was aliquoted and stored as single-use aliquots at −80°C. The baseline measurements for Aβ(1–40), Aβ(1–42), and total Tau protein (T-Tau) concentrations for each sample were done within 3 months of blood draw by IMR. They are referred to as baseline concentrations. A separate aliquot from each sample was assayed with IMR to assess the stability of the measured analytes during storage at −80°C between 1.1 and 5.4 years. This is referred to as a repeated result. RESULTS: IMR shows that plasma levels of Aβ(1–40) and Aβ(1–42) exhibit stability over 5-year storage at −80°C and that plasma levels of T-Tau are less stable (approximately 1.5 years). CONCLUSION: Although the measured concentrations of T-Tau in human plasma may alter during storage, the diagnostic utility of the results are only slightly affected when the product of Aβ(1–42) and T-Tau concentrations are used. The results show that the overall agreement between baseline and repeated measurements in the ability of discriminating NCs from aMCI/AD patients is higher than 80%. S. Karger AG 2019-02-12 /pmc/articles/PMC6477481/ /pubmed/31043966 http://dx.doi.org/10.1159/000496099 Text en Copyright © 2019 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes as well as any distribution of modified material requires written permission.
spellingShingle Original Research Article
Chiu, Ming-Jang
Lue, Lih-Fen
Sabbagh, Marwan N.
Chen, Ta-Fu
Chen, H.H.
Yang, Shieh-Yueh
Long-Term Storage Effects on Stability of Aβ(1–40), Aβ(1–42), and Total Tau Proteins in Human Plasma Samples Measured with Immunomagnetic Reduction Assays
title Long-Term Storage Effects on Stability of Aβ(1–40), Aβ(1–42), and Total Tau Proteins in Human Plasma Samples Measured with Immunomagnetic Reduction Assays
title_full Long-Term Storage Effects on Stability of Aβ(1–40), Aβ(1–42), and Total Tau Proteins in Human Plasma Samples Measured with Immunomagnetic Reduction Assays
title_fullStr Long-Term Storage Effects on Stability of Aβ(1–40), Aβ(1–42), and Total Tau Proteins in Human Plasma Samples Measured with Immunomagnetic Reduction Assays
title_full_unstemmed Long-Term Storage Effects on Stability of Aβ(1–40), Aβ(1–42), and Total Tau Proteins in Human Plasma Samples Measured with Immunomagnetic Reduction Assays
title_short Long-Term Storage Effects on Stability of Aβ(1–40), Aβ(1–42), and Total Tau Proteins in Human Plasma Samples Measured with Immunomagnetic Reduction Assays
title_sort long-term storage effects on stability of aβ(1–40), aβ(1–42), and total tau proteins in human plasma samples measured with immunomagnetic reduction assays
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477481/
https://www.ncbi.nlm.nih.gov/pubmed/31043966
http://dx.doi.org/10.1159/000496099
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