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An antibody microarray analysis of serum cytokines in neurodegenerative Parkinsonian syndromes

BACKGROUND: Microarray technology may offer a new opportunity to gain insight into disease-specific global protein expression profiles. The present study was performed to apply a serum antibody microarray to screen for differentially regulated cytokines in Parkinson's disease (PD), multiple sys...

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Autores principales: Mahlknecht, Philipp, Stemberger, Sylvia, Sprenger, Fabienne, Rainer, Johannes, Hametner, Eva, Kirchmair, Rudolf, Grabmer, Christoph, Scherfler, Christoph, Wenning, Gregor K, Seppi, Klaus, Poewe, Werner, Reindl, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539904/
https://www.ncbi.nlm.nih.gov/pubmed/23173604
http://dx.doi.org/10.1186/1477-5956-10-71
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author Mahlknecht, Philipp
Stemberger, Sylvia
Sprenger, Fabienne
Rainer, Johannes
Hametner, Eva
Kirchmair, Rudolf
Grabmer, Christoph
Scherfler, Christoph
Wenning, Gregor K
Seppi, Klaus
Poewe, Werner
Reindl, Markus
author_facet Mahlknecht, Philipp
Stemberger, Sylvia
Sprenger, Fabienne
Rainer, Johannes
Hametner, Eva
Kirchmair, Rudolf
Grabmer, Christoph
Scherfler, Christoph
Wenning, Gregor K
Seppi, Klaus
Poewe, Werner
Reindl, Markus
author_sort Mahlknecht, Philipp
collection PubMed
description BACKGROUND: Microarray technology may offer a new opportunity to gain insight into disease-specific global protein expression profiles. The present study was performed to apply a serum antibody microarray to screen for differentially regulated cytokines in Parkinson's disease (PD), multiple system atrophy (MSA), progressive supranuclear palsy (PSP) and corticobasal syndrome (CBS). RESULTS: Serum samples were obtained from patients with clinical diagnoses of PD (n = 117), MSA (n = 31) and PSP/CBS (n = 38) and 99 controls. Cytokine profiles of sera from patients and controls were analyzed with a semiquantitative human antibody array for 174 cytokines and the expression of 12 cytokines was found to be significantly altered. In a next step, results from the microarray experiment were individually validated by different immunoassays. Immunoassay validation confirmed a significant increase of median PDGF-BB levels in patients with PSP/CBS, MSA and PD and a decrease of median prolactin levels in PD. However, neither PDGF-BB nor prolactin were specific biomarkers to discriminate PSP/CBS, MSA, PD and controls. CONCLUSIONS: In our unbiased cytokine array based screening approach and validation by a different immunoassay only two of 174 cytokines were significantly altered between patients and controls.
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spelling pubmed-35399042013-01-10 An antibody microarray analysis of serum cytokines in neurodegenerative Parkinsonian syndromes Mahlknecht, Philipp Stemberger, Sylvia Sprenger, Fabienne Rainer, Johannes Hametner, Eva Kirchmair, Rudolf Grabmer, Christoph Scherfler, Christoph Wenning, Gregor K Seppi, Klaus Poewe, Werner Reindl, Markus Proteome Sci Research BACKGROUND: Microarray technology may offer a new opportunity to gain insight into disease-specific global protein expression profiles. The present study was performed to apply a serum antibody microarray to screen for differentially regulated cytokines in Parkinson's disease (PD), multiple system atrophy (MSA), progressive supranuclear palsy (PSP) and corticobasal syndrome (CBS). RESULTS: Serum samples were obtained from patients with clinical diagnoses of PD (n = 117), MSA (n = 31) and PSP/CBS (n = 38) and 99 controls. Cytokine profiles of sera from patients and controls were analyzed with a semiquantitative human antibody array for 174 cytokines and the expression of 12 cytokines was found to be significantly altered. In a next step, results from the microarray experiment were individually validated by different immunoassays. Immunoassay validation confirmed a significant increase of median PDGF-BB levels in patients with PSP/CBS, MSA and PD and a decrease of median prolactin levels in PD. However, neither PDGF-BB nor prolactin were specific biomarkers to discriminate PSP/CBS, MSA, PD and controls. CONCLUSIONS: In our unbiased cytokine array based screening approach and validation by a different immunoassay only two of 174 cytokines were significantly altered between patients and controls. BioMed Central 2012-11-23 /pmc/articles/PMC3539904/ /pubmed/23173604 http://dx.doi.org/10.1186/1477-5956-10-71 Text en Copyright ©2012 Mahlknecht et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Mahlknecht, Philipp
Stemberger, Sylvia
Sprenger, Fabienne
Rainer, Johannes
Hametner, Eva
Kirchmair, Rudolf
Grabmer, Christoph
Scherfler, Christoph
Wenning, Gregor K
Seppi, Klaus
Poewe, Werner
Reindl, Markus
An antibody microarray analysis of serum cytokines in neurodegenerative Parkinsonian syndromes
title An antibody microarray analysis of serum cytokines in neurodegenerative Parkinsonian syndromes
title_full An antibody microarray analysis of serum cytokines in neurodegenerative Parkinsonian syndromes
title_fullStr An antibody microarray analysis of serum cytokines in neurodegenerative Parkinsonian syndromes
title_full_unstemmed An antibody microarray analysis of serum cytokines in neurodegenerative Parkinsonian syndromes
title_short An antibody microarray analysis of serum cytokines in neurodegenerative Parkinsonian syndromes
title_sort antibody microarray analysis of serum cytokines in neurodegenerative parkinsonian syndromes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539904/
https://www.ncbi.nlm.nih.gov/pubmed/23173604
http://dx.doi.org/10.1186/1477-5956-10-71
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