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An antibody microarray analysis of serum cytokines in neurodegenerative Parkinsonian syndromes.


ABSTRACT: UNLABELLED: 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.

SUBMITTER: Mahlknecht P 

PROVIDER: S-EPMC3539904 | biostudies-literature | 2012 Nov

REPOSITORIES: biostudies-literature

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<h4>Unlabelled</h4><h4>Background</h4>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).<h4>Results</h4>Serum samples were obtained from patients with clinical diagnoses of PD (n   ...[more]

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