Quantitative Proteomic (iTRAQ) Analysis of 1st Trimester Maternal Plasma Samples in Pregnancies at Risk for Preeclampsia.

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...

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Published in:Journal of Biomedicine & Biotechnology Vol. 2012; pp. 1 - 9
Main Authors: Kolla, Varaprasad, Jenö, Paul, Moes, Suzette, Lapaire, Olav, Hoesli, Irene, Hahn, Sinuhe
Format: research tables/charts Journal Article
Published: Wiley-Blackwell 2012
Online Access:View this record in EBSCOhost
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      dt: 2012
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        atl: Quantitative Proteomic (iTRAQ) Analysis of 1st Trimester Maternal Plasma Samples in Pregnancies at Risk for Preeclampsia.
      aug:
        au:
          Kolla, Varaprasad
          Jenö, Paul
          Moes, Suzette
          Lapaire, Olav
          Hoesli, Irene
          Hahn, Sinuhe
        affil: Department of Biomedicine, University Women's Hospital, 4031 Basel, Switzerland
      sug:
        subj:
          Pre-Eclampsia Risk Factors
          Proteomics Methods
          Pregnancy Trimester, First
          Biological Markers Blood
          Human
          Female
          Quantitative Studies
          Prenatal Diagnosis Methods
          Pregnancy
          Peptides Blood
          Pilot Studies
          Fibrinogen
          Angiotensins Blood
          Funding Source
          Adult
          Adult: 19-44 years
          Female
      ab: 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 fromwomen 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.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
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      ougenre: Article
    language: English
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