Placental specific mRNA in the maternal circulation are globally dysregulated in pregnancies complicated by fetal growth restriction.
Whitehead. Clare L CL; Walker. Susan P SP; Ye. Louie L; Mendis. Sonali S; Kaitu'u-Lino. Tu'uhevaha J TJ; Lappas. Martha M; Tong. Stephen S
Key Findings
- 137 placenta‑specific genes were identified and detectable in maternal blood
- 75 of these genes were significantly altered in severe preterm fetal growth restriction
- KISS1 (kisspeptin) and several other genes were consistently higher in both blood and placenta of affected pregnancies
Practical Outcomes
- The main takeaway is that placental mRNA, including kisspeptin‑related KISS1, might become a future biomarker for spotting dangerous fetal growth issues early. For biohackers, there’s no immediate protocol or dosage recommendation; the finding is primarily relevant for clinical diagnostics, not personal health optimization.
Summary
Scientists found that a set of genes that are normally active only in the placenta, including the KISS1 gene that makes kisspeptin, show abnormal levels in the blood of pregnant women whose babies have severe growth problems. This suggests these placental RNAs could become a blood test for early detection of fetal growth restriction, but it doesn’t give any direct advice for health‑hacking or personal use of kisspeptin.
Abstract
Fetal growth restriction (FGR) is a leading cause of perinatal mortality, yet no reliable screening test exists. Placental specific mRNA in the maternal circulation may reflect changes in the placental transcriptome in FGR and could be a novel biomarker for FGR. The aim of the study was to identify placental specific RNA detectable in the maternal circulation and examine whether they are differentially expressed in severe preterm FGR. In silico screening was used to identify placental specific RNAs. Their expression in cases of severe FGR vs controls was examined in both maternal blood and placenta by microarray, RT-PCR, and in situ hybridization. Via in silico analysis, we identified 137 genes very highly expressed in the placenta relative to other tissues. Using microarray, we found that they were detectable in the maternal blood and were globally dysregulated with preterm FGR; 75 genes (55%) had a ≥1.5-fold differential expression compared to controls. Eight genes (ERVWE-1, PSG1, PLAC4, TAC3, PLAC3, CRH, CSH1, and KISS1) were validated by RT-PCR to be significantly increased in both maternal blood and placenta in a larger cohort of severe FGR compared to controls. In situ hybridization confirmed PAPPA2 and ERVWE-1 localized to the syncytiotrophoblast. There is global differential expression of placental specific mRNA in the maternal blood in pregnancies complicated by severe preterm FGR. Placental specific mRNA in maternal blood may represent a new class of biomarkers for preterm FGR.
Study Information
pubmed
2013
2013-01-21T00:00:00.000Z
10.1210/jc.2012-2468
58
32