Absolute and relative quantification of placenta-specific micrornas in maternal circulation with placental insufficiency-related complications
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22251611
DOI
10.1016/j.jmoldx.2011.11.003
PII: S1525-1578(11)00317-5
Knihovny.cz E-resources
- MeSH
- Pregnancy Complications etiology pathology MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Humans MeSH
- MicroRNAs blood genetics MeSH
- Placenta metabolism MeSH
- Placental Insufficiency genetics MeSH
- Pre-Eclampsia etiology pathology MeSH
- Retrospective Studies MeSH
- Fetal Growth Retardation etiology pathology MeSH
- Case-Control Studies MeSH
- Pregnancy MeSH
- Check Tag
- Humans MeSH
- Pregnancy MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- MicroRNAs MeSH
Placental insufficiency-related complications are one of the leading causes of maternal and perinatal morbidity and mortality. This study investigated the quantification of placenta-specific microRNAs (miRNAs) in the maternal circulation during gestation in a cohort of women with normally progressing pregnancies, the differentiation between placental insufficiency-related complications and normally progressing pregnancies, and the differentiation between placental insufficiency and normally progressing pregnancies during the early stages of gestation. Both absolute and relative quantification of placenta-specific miRNAs (ie, miR-516-5p, miR-517*, miR-518b, miR-520a*, miR-520h, miR-525, and miR-526a) was determined in 50 women with normally progressing pregnancies, 32 with complicated pregnancies [21 with preeclampsia with or without intrauterine growth retardation (IUGR) and 11 with IUGR], and 7 women with pregnancies at various gestational stages who later developed preeclampsia and/or IUGR using real-time PCR and a comparative C(T) method relative to normalization factor (ie, geometric mean of ubiquitous miR-16 and let-7d). Both quantification approaches revealed significant increases in extracellular placenta-specific miRNA levels over time in women with normally progressing pregnancies; however, they were not able to differentiate between normally progressing and complicated pregnancies at the time of preeclampsia and/or IUGR onset. Nevertheless, significant elevation of extracellular miRNA levels was observed during early gestation (ie, within the 12th to 16th weeks) in pregnancies with later onset of preeclampsia and/or IUGR. Early gestation extracellular miRNA screening can differentiate between women with normally progressing pregnancies and those who may later develop placental insufficiency-related complications.
References provided by Crossref.org
Genome-wide miRNA profiling in plasma of pregnant women with down syndrome fetuses
Expression profile of C19MC microRNAs in placental tissue in pregnancy-related complications
Extracellular chromosome 21-derived microRNAs in euploid & aneuploid pregnancies
Circulating C19MC microRNAs in preeclampsia, gestational hypertension, and fetal growth restriction