Quantitative distribution of a panel of circulating mRNA in preeclampsia versus controls

• Published in: Prenatal diagnosis Vol. 26; no. 12; pp. 1115 - 1120
• Main Authors: Farina, Antonio, Sekizawa, Akihiko, Purwosunu, Yuditiya, Rizzo, Nicola, Banzola, Irina, Concu, Manuela, Morano, Danila, Giommi, Federica, Bevini, Maurizio, Mabrook, Mohamad, Carinci, Paolo, Okai, Takashi
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Ltd 01.12.2006; Wiley
• Subjects: Biological and medical sciences; Biomarkers - blood; Case-Control Studies; circulating mRNA; Diseases of mother, fetus and pregnancy; Female; Fetal Growth Retardation - genetics; Gestational Age; Gynecology. Andrology. Obstetrics; Humans; Inhibins - genetics; Kisspeptins; Management. Prenatal diagnosis; Medical sciences; molecular markers; multivariable screening; P-Selectin - genetics; Placental Lactogen - genetics; Plasminogen Activator Inhibitor 1 - genetics; Pre-Eclampsia - genetics; preeclampsia; Pregnancy; Pregnancy Trimester, Third; Pregnancy-Associated Plasma Protein-A - genetics; Pregnancy. Fetus. Placenta; real‐time PCR; Receptors, Vascular Endothelial Growth Factor - genetics; Reference Values; RNA, Messenger - blood; Tumor Suppressor Proteins - genetics; multivariable screening; Pregnancy disorders; Genetic marker; Prenatal Diagnosis; Molecular marker; real-time PCR; Medical screening; Real time; circulating mRNA; Pregnancy toxemia; Polymerase chain reaction; Messenger RNA; Preeclampsia; Distribution; Molecular biology; molecular markers; Comparative study; Quantitative analysis
• DOI: 10.1002/pd.1562
• ISSN: 0197-3851

Objective The aim of this study was to evaluate whether the quantitative distribution of a panel of circulating mRNAs from maternal whole blood of normal pregnancies is statistically different from those complicated with preeclampsia (PE) with or without intrauterine growth restriction (IUGR). Methods Maternal whole blood of six subjects with mild or severe PE with or without IUGR and 30 matched controls (1:5 match for gestational age) were retrospectively examined for circulating mRNA markers. Seven specific mRNA markers were identified and chosen based on previous microarray mRNA expressions performed on placental tissue from normal and PE patients. They were human placental lactogen (hPL), inhibin A, KISS‐1, pregnancy‐associated plasma protein‐A (PAPP‐A), plasminogen activator inhibitor type 1 (PAI‐1), selectin‐P and vascular endothelial growth factor receptor (VEGFR), which were therefore quantified for statistical purposes. Results Median gestational age was 229 (178–283) and 232 (194–262) days for controls and cases respectively. All mRNA markers but PAPP‐A, showed statistically different median values. They were hPL, inhibin A, KISS‐1, PAI‐1, Selectin‐P, and VEGFR. Inhibin A, Selectin‐P and VEGFR showed higher values than expected for controls. Instead, hPL, KISS‐1 and PAI‐1 values of PE patients were lower than those of controls. Selectin‐P was the marker with the most aberrant difference, followed by VEGFR and KISS‐1. Conclusion This preliminary analysis revealed that the median values of a panel of mRNAs from the maternal blood of PE patients were different from those of the same gestational age control group at the third trimester. If prospective studies at the second trimester could detect a related marker sufficiently able to discriminate between affected and unaffected patients and thus detect the disease before its clinical onset, then a screening project using a panel of mRNAs would be feasible. Copyright © 2006 John Wiley & Sons, Ltd.