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Quantitative proteomic (iTRAQ) analysis of 1st trimester maternal plasma samples in pregnancies at risk for preeclampsia
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 2343449
Author(s) Kolla, Varaprasad; Jenö, Paul; Moes, Suzette; Lapaire, Olav; Hoesli, Irene; Hahn, Sinuhe
Author(s) at UniBasel Jenö, Paul
Hahn, Sinuhe
Year 2012
Title Quantitative proteomic (iTRAQ) analysis of 1st trimester maternal plasma samples in pregnancies at risk for preeclampsia
Journal Journal of biomedicine and biotechnolgy
Volume 2012
Pages / Article-Number 305964
Keywords Databases, Protein; Female; Humans; Peptide Fragments/blood; Pre-Eclampsia/*blood/metabolism; Pregnancy; Pregnancy Trimester, First/*blood; Prenatal Diagnosis/*methods; Proteome/metabolism; Proteomics/methods; Retrospective Studies; Tandem Mass Spectrometry
Abstract

A current major obstacle is that no reliable screening markers exist to detect pregnancies at risk for preeclampsia. Quantitative proteomic analysis employing isobaric labelling (iTRAQ) has been suggested to be suitable for the detection of potential plasma biomarkers, a feature we recently verified in analysis of pregnancies with Down syndrome foetuses. We have now examined whether this approach could yield biomarkers to screen pregnancies at risk for preeclampsia. In our study, we used maternal plasma samples obtained at 12 weeks of gestation, six from women who subsequently developed preeclampsia and six with uncomplicated deliveries. In our analysis, we observed elevations in 10 proteins out of 64 proteins in the preeclampsia study group when compared to the healthy control group. These proteins included clusterin, fibrinogen, fibronectin, and angiotensinogen, increased levels of which are known to be associated with preeclampsia. An elevation in the immune-modulatory molecule, galectin 3 binding protein, was also noted. Our pilot study, therefore, indicates that quantitative proteomic iTRAQ analysis could be a useful tool for the detection of new preeclampsia screening markers.

Publisher Hindawi
ISSN/ISBN 1110-7243
URL http://www.ncbi.nlm.nih.gov/pubmed/22570525
edoc-URL http://edoc.unibas.ch/dok/A6212392
Full Text on edoc Available
Digital Object Identifier DOI 10.1155/2012/305964
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/22570525
ISI-Number MEDLINE:22570525
Document type (ISI) Journal Article
 
   

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