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Gene expression profiling of placentae from women with early- and late-onset pre-eclampsia: down-regulation of the angiogenesis related genes ACVRL1 and EGFL7 in early-onset disease
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Women's and Children's Health.
Lunds universitet, Medicinska fakulteten, Institutionen för kliniska vetenskaper, Lund, Avdelningen för obstetrik och gynekologi.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Women's and Children's Health. (Obstetrisk forskning/Axelsson)
Lunds universitet, Medicinska fakulteten, Institutionen för kliniska vetenskaper, Lund, Avdelningen för obstetrik och gynekologi.
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2012 (English)In: Molecular human reproduction, ISSN 1360-9947, E-ISSN 1460-2407, Vol. 18, no 3, 146-155 p.Article in journal (Refereed) Published
Abstract [en]

The underlying mechanisms behind the obstetric condition pre-eclampsia (PE) are still unclear. Manifestation of PE is heterogeneous and it has therefore been proposed to be a syndrome with different causes rather than one disease with a specific aetiology. Recently, we showed differences in circulating angiogenic factors between two subgroups - early- and late-onset PE. To further elucidate the differences between the two, we investigated placental gene expression profiles. Whole genome microarray technology and bioinformatic analysis were used to evaluate gene expression profiles in placentae from early- (24-32 gestational weeks, n=8) and late-onset (36-41 gestational weeks, n=7) PE. The results were verified by using quantitative real-time PCR. We found significant differences in the expression of 196 genes in early- compared with late-onset PE, 45 of these genes showing a fold change above 2. Bioinformatic analysis revealed alterations in angiogenesis and regulation of cell motility. Two angiogenesis-associated transcripts (Egfl7 and Acvrl1) showed lower expression in early-onset PE vs. late-onset PE (p=0.037 and p=0.003) and vs. gestational age-matched controls (p=0.007 and p=0.011). We conclude that angiogenesis-associated genes are regulated in a different manner in the two subgroups, and that the gene expression profiles of early- and late-onset PE diverge, supporting the hypothesis of early- and late-onset PE being at least partly two separate entities.

Place, publisher, year, edition, pages
2012. Vol. 18, no 3, 146-155 p.
Keyword [en]
angiogenesis, early-onset pre-eclampsia, gene expression, microarray, placenta
National Category
Medical and Health Sciences
Identifiers
URN: urn:nbn:se:uu:diva-161107DOI: 10.1093/molehr/gar067ISI: 000300726400005PubMedID: 22013081OAI: oai:DiVA.org:uu-161107DiVA: diva2:454474
Available from: 2011-11-07 Created: 2011-11-07 Last updated: 2017-12-08Bibliographically approved

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Junus, KatjaWikström, Anna-KarinOlovsson, Matts

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