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Microarray screening for novel preeclampsia biomarker candidates
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 2833262
Author(s) Lapaire, O.; Grill, S.; Lalevee, S.; Kolla, V.; Hosli, I.; Hahn, S.
Author(s) at UniBasel Hahn, Sinuhe
Year 2012
Title Microarray screening for novel preeclampsia biomarker candidates
Journal Fetal diagnosis and therapy
Volume 31
Number 3
Pages / Article-Number 147-53
Keywords Screening, Biomarkers, Preeclampsia, Pregnancy
Abstract INTRODUCTION: Our aim was to identify novel biomarker candidates for the near-term prediction of preeclampsia in a homogenous collective. In this study, we screened at the genome-wide level for gene expression in placental villous tissue from patients with severe preeclampsia in comparison to normal healthy pregnancies. MATERIAL AND METHODS: Total RNA was extracted from placental villous tissue from 9 preeclamptic patients and 7 normotensive controls after scheduled cesarean sections. After sample pooling, gene expression analysis was performed using six Affymetrix Human Gene 1.0 ST arrays, followed by quantitative RT-PCR and validation of selected markers in the serum of patients at the protein level. RESULTS: In total, 896 significantly differentially expressed genes were identified (p >/= 0.05). After restricting these to molecules present in the circulation, 9 upregulated and 5 downregulated genes were selected. Four of them (beta-hCG, HTRA4, LHB1, all upregulated; and NOX4, downregulated) were validated by quantitative real-time RT-PCR. Finally, the maternal plasma protein levels of 2 of these genes (LHB and beta-hCG) were confirmed to be significantly different between preeclampsia cases and controls. DISCUSSION: We identified 14 potential new biomarker candidates for preeclampsia and validated 4 of them by quantitative RT-PCR and 2 of them with subsequent serum protein analyses. Further studies will assess the optimal marker combination for the imminent prediction of impending preeclampsia.
Publisher Karger
ISSN/ISBN 1015-3837 ; 1421-9964
edoc-URL http://edoc.unibas.ch/dok/A6338568
Full Text on edoc Available
Digital Object Identifier DOI 10.1159/000337325
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/22472943
ISI-Number WOS:000303363300002
Document type (ISI) Journal Article
 
   

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