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Updated: Jun 28, 2026

The 4-vessel Sampling Approach to Integrative Studies of Human Placental Physiology In Vivo
Published on: August 2, 2017
Gene expression of placental hormones regulating energy balance in small for gestational age neonates
Ellen Struwe1, Gabriele M Berzl, Ralf L Schild
1Department of Pediatrics, University Hospital of Erlangen-Nuremberg, Germany.
Insights
Placental leptin increased in small for gestational age (SGA) neonates and correlated inversely with birth weight. Other hormones showed no change, questioning their role in fetal programming.
Area of Science:
- Endocrinology
- Perinatal Medicine
- Developmental Biology
Background:
- Fetal growth restriction (FGR) is linked to later metabolic and cardiovascular disease.
- Prenatal programming mechanisms require further investigation.
- Placental hormones like leptin, resistin, adiponectin, and ghrelin may play a role.
Purpose of the Study:
- To measure placental levels of leptin, resistin, adiponectin, and ghrelin in small for gestational age (SGA) neonates.
- To investigate the relationship between these hormones and fetal growth.
- To elucidate potential mechanisms of prenatal programming.
Main Methods:
- Comparative analysis of 16 SGA placentas versus 24 appropriate for gestational age (AGA) placentas.
- Quantification of placental mRNA gene expression for leptin, resistin, adiponectin, and ghrelin.
- Western blot analysis for protein expression of hormones showing altered gene regulation.
Main Results:
- Significantly increased placental mRNA and protein expression of leptin in SGA neonates.
- No significant differences in placental resistin, adiponectin, or ghrelin expression between SGA and AGA groups.
- Leptin demonstrated a significant inverse correlation with birth weight; adiponectin correlated with leptin and ghrelin.
Conclusions:
- Elevated placental leptin in SGA neonates correlates with lower birth weight.
- Unchanged expression of resistin, adiponectin, and ghrelin in SGA placentas suggests a limited role in fetal programming.
- Interactions between adiponectin, leptin, and ghrelin in the placenta warrant further study.
Objective:
Fetal growth restriction is associated with an increased risk for metabolic and cardiovascular disease in later life. To further elucidate mechanisms that might be involved in the process of prenatal programming, we measured the adipokines leptin, resistin, and adiponectin and the GH-releasing hormone ghrelin in the placenta of small for gestational age (SGA) neonates.
Study Design:
The control group included 24 placentas of appropriate for gestational age (AGA) newborns, in the study group were 16 placentas of SGA neonates. Gene expression of leptin, resistin, adiponectin, and ghrelin was examined. For hormones showing alterations in gene regulation placental protein expression was measured by Western blot.
Results:
Placental mRNA expression of leptin was significantly increased in SGA placentas (p=0.0035, related to beta-actin). Protein concentration was increased, as well. There were no differences in placental resistin, adiponectin, or ghrelin gene expressions between SGA neonates and controls. Leptin was the only hormone to demonstrate a significant inverse correlation with birth weight (r=-0.44, p=0.01). Adiponectin correlated significantly with leptin (r=0.53, p=0.0023) and ghrelin (r=0.50, p=0.0045).
Conclusions:
Placental leptin gene expression and protein concentration showed the expected increase in the SGA group. Leptin was inversely correlated with birth weight. Positive correlation of adiponectin with leptin and ghrelin expression suggests an interaction between these hormones in the placenta. However, the unchanged expression of resistin, adiponectin, and ghrelin in SGA placentas and the absence of correlation with birth weight cast doubt whether these hormones produced in the placenta play a key role in fetal programming.
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