Placental LPL gene expression is increased in severe intrauterine growth-restricted pregnancies

47Citations
Citations of this article
26Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Intrauterine growth restriction (IUGR) is associated with reduced placental supply of nutrients to the fetus. lipoprotein lipase (LPL) mediates the hydrolysis of triglycerides from maternal lipoproteins to obtain fatty acids. Here, we tested the hypothesis that placental LPL gene expression level is altered in pregnancies complicated by IUGR. To this purpose, 28 IUGR fetuses were identified during pregnancy and divided in two groups: 7 M-IUGR ["mild" IUGR, with normal umbilical artery pulsatility index (PI)] and 21 S-IUGR ("severe" IUGR, with abnormal PI). Moreover, 10 out of 28 IUGR pregnancies were associated with preeclampsia. Controls were 19 normal pregnancies delivering appropriate for gestational age (AGA) fetuses. Relative real-time quantification of LPL was carried out in RNA from placental chorionic villi by the ΔΔCt method, using β-actin as normalizing gene. Placental LPL mRNA expression levels were significantly higher in IUGR than in AGA. In particular, significantly higher values were observed in S-IUGR, independent from the concomitant association with preeclampsia. No significant relationship was observed between placental LPL mRNA expression levels or gestational age. In conclusion, placental LPL mRNA gene expression is increased in severe IUGR, characterized by enhanced vascular placental resistances and alterations of placental nutrient transport. Copyright © 2006 International Pediatric Research Foundation, Inc.

Cite

CITATION STYLE

APA

Tabano, S., Alvino, G., Antonazzo, P., Grati, F. R., Miozzo, M., & Cetin, I. (2006). Placental LPL gene expression is increased in severe intrauterine growth-restricted pregnancies. Pediatric Research, 59(2), 250–253. https://doi.org/10.1203/01.pdr.0000199441.62045.a1

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free