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Comparison of Two Analytical Platforms for CSF Biomarkers of Alzheimer's Disease

Cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease (AD) are currently being assessed with two different assays. Our objective was to study if there is a correlation between values obtained by both techniques, to compare their validity and search for conversion factor between values obt...

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Autores principales: Monge-Argilés, Jose Antonio, Muñoz-Ruiz, Carlos, Sánchez-Payá, José, Gasparini Berenguer, Ruth, Blanco Cantó, Maria Empar, Leiva-Santana, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058141/
https://www.ncbi.nlm.nih.gov/pubmed/24971348
http://dx.doi.org/10.1155/2014/765130
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author Monge-Argilés, Jose Antonio
Muñoz-Ruiz, Carlos
Sánchez-Payá, José
Gasparini Berenguer, Ruth
Blanco Cantó, Maria Empar
Leiva-Santana, Carlos
author_facet Monge-Argilés, Jose Antonio
Muñoz-Ruiz, Carlos
Sánchez-Payá, José
Gasparini Berenguer, Ruth
Blanco Cantó, Maria Empar
Leiva-Santana, Carlos
author_sort Monge-Argilés, Jose Antonio
collection PubMed
description Cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease (AD) are currently being assessed with two different assays. Our objective was to study if there is a correlation between values obtained by both techniques, to compare their validity and search for conversion factor between values obtained for every protein. We compared the performances of two commonly used platforms, an enzyme-linked immunosorbent assay (ELISA) and a multiplex (xMAP) technology for measurement of CSF Aβ (1–42), total tau (T-tau), and phosphorylated tau 181 (P-tau(181p)) proteins, in 30 AD patients and 28 control subjects. The relations between the variables of both techniques were evaluated using the Spearman p correlation coefficient (α = 0.05). Receiver operating characteristic and area under the curve (AUC) analyses were calculated for the variables of both techniques. The two assays platforms yielded different absolute values for the various analytes, always higher in ELISA. We found some correction factor between values: 2,1- to 3-fold for Aβ (1–42); 4,1- to 4,6-fold for T-tau; and 1,4- to 1,6-fold for P-tau(181p). In addition, those values were highly correlated (Aβ (1–42): r = 0.70, P < 0.01; T-tau: r = 0.90, P < 0.01; P-tau(181p): r = 0.85, P < 0.01) and the AUC for the variables showed very similar values. In conclusion, the results obtained with ELISA and xMAP platforms were highly correlated and its validity is very similar. Differences in absolute values point to the need for a clear description of the technique used. Moreover, we found some conversion factor between values of every protein that may be useful for transformation between both techniques.
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spelling pubmed-40581412014-06-26 Comparison of Two Analytical Platforms for CSF Biomarkers of Alzheimer's Disease Monge-Argilés, Jose Antonio Muñoz-Ruiz, Carlos Sánchez-Payá, José Gasparini Berenguer, Ruth Blanco Cantó, Maria Empar Leiva-Santana, Carlos Biomed Res Int Research Article Cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease (AD) are currently being assessed with two different assays. Our objective was to study if there is a correlation between values obtained by both techniques, to compare their validity and search for conversion factor between values obtained for every protein. We compared the performances of two commonly used platforms, an enzyme-linked immunosorbent assay (ELISA) and a multiplex (xMAP) technology for measurement of CSF Aβ (1–42), total tau (T-tau), and phosphorylated tau 181 (P-tau(181p)) proteins, in 30 AD patients and 28 control subjects. The relations between the variables of both techniques were evaluated using the Spearman p correlation coefficient (α = 0.05). Receiver operating characteristic and area under the curve (AUC) analyses were calculated for the variables of both techniques. The two assays platforms yielded different absolute values for the various analytes, always higher in ELISA. We found some correction factor between values: 2,1- to 3-fold for Aβ (1–42); 4,1- to 4,6-fold for T-tau; and 1,4- to 1,6-fold for P-tau(181p). In addition, those values were highly correlated (Aβ (1–42): r = 0.70, P < 0.01; T-tau: r = 0.90, P < 0.01; P-tau(181p): r = 0.85, P < 0.01) and the AUC for the variables showed very similar values. In conclusion, the results obtained with ELISA and xMAP platforms were highly correlated and its validity is very similar. Differences in absolute values point to the need for a clear description of the technique used. Moreover, we found some conversion factor between values of every protein that may be useful for transformation between both techniques. Hindawi Publishing Corporation 2014 2014-05-29 /pmc/articles/PMC4058141/ /pubmed/24971348 http://dx.doi.org/10.1155/2014/765130 Text en Copyright © 2014 Jose Antonio Monge-Argilés et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Monge-Argilés, Jose Antonio
Muñoz-Ruiz, Carlos
Sánchez-Payá, José
Gasparini Berenguer, Ruth
Blanco Cantó, Maria Empar
Leiva-Santana, Carlos
Comparison of Two Analytical Platforms for CSF Biomarkers of Alzheimer's Disease
title Comparison of Two Analytical Platforms for CSF Biomarkers of Alzheimer's Disease
title_full Comparison of Two Analytical Platforms for CSF Biomarkers of Alzheimer's Disease
title_fullStr Comparison of Two Analytical Platforms for CSF Biomarkers of Alzheimer's Disease
title_full_unstemmed Comparison of Two Analytical Platforms for CSF Biomarkers of Alzheimer's Disease
title_short Comparison of Two Analytical Platforms for CSF Biomarkers of Alzheimer's Disease
title_sort comparison of two analytical platforms for csf biomarkers of alzheimer's disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058141/
https://www.ncbi.nlm.nih.gov/pubmed/24971348
http://dx.doi.org/10.1155/2014/765130
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