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Author Spotlight: Modeling an Aspect of Preeclampsia in Female Mice Using Hypoxic Human Placenta-Derived Small Extracellular Vesicles
Published on: January 26, 2024
Early-pregnancy transcriptome signatures of preeclampsia: from peripheral blood to placenta
Aishwarya P Yadama1, Enrico Maiorino1, Vincent J Carey1
1Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Insights
Maternal asthma, excess BMI, and low vitamin D increase preeclampsia risk. Shared gene signatures in blood and placenta link these conditions, offering potential for early preeclampsia prediction.
Area of Science:
- Reproductive biology
- Immunology
- Genetics
Background:
- Preeclampsia (PE) risk is associated with maternal asthma, high body mass index (BMI), and vitamin D insufficiency.
- Previous research suggests potential links between these conditions.
Purpose of the Study:
- To investigate shared peripheral blood and placental gene expression signatures connecting PE, maternal asthma, vitamin D insufficiency, and excess BMI.
- To identify potential pre-clinical biomarkers for PE prediction.
Main Methods:
- Analysis of peripheral blood gene expression from the Vitamin D Antenatal Asthma Reduction Trial (VDAART) cohort.
- Validation of gene signatures in peripheral blood and placental tissues from independent cohorts.
- Construction of a PE module using protein-protein interaction networks.
Main Results:
- A core set of differentially expressed genes was identified across all four conditions (PE, asthma, low vitamin D, high BMI) in peripheral blood.
- These shared gene signatures were confirmed in placental tissue.
- CXC chemokine genes exhibited high connectivity and centrality in both peripheral blood and placental networks.
Conclusions:
- Shared gene signatures highlight biological pathways involved in preeclampsia during the pre-clinical stage.
- These findings suggest potential for early PE prediction using identified biomarkers.
Abstract:
Several studies have linked maternal asthma, excess BMI, and low vitamin D status with increased risk of Preeclampsia (PE) development. Given prior evidence in the literature and our observations from the subjects in the Vitamin D Antenatal Asthma Reduction Trial (VDAART), we hypothesized that PE, maternal asthma, vitamin D insufficiency, and excess body mass index (BMI) might share both peripheral blood and placental gene signatures that link these conditions together. We used samples collected in the VDAART to investigate relationships between these four conditions and gene expression patterns in peripheral blood obtained at early pregnancy. We identified a core set of differentially expressed genes in all comparisons between women with and without these four conditions and confirmed them in two separate sets of samples. We confirmed the differential expression of the shared gene signatures in the placenta from an independent study of preeclampsia cases and controls and constructed the preeclampsia module using protein-protein interaction networks. CXC chemokine genes showed the highest degrees of connectivity and betweenness centrality in the peripheral blood and placental modules. The shared gene signatures demonstrate the biological pathways involved in preeclampsia at the pre-clinical stage and may be used for the prediction of preeclampsia.

