Signs of immune dysregulation in second-trimester maternal blood RNA profiles in late-onset preeclampsia

Preeclampsia (PE) is a hypertensive disorder that affects 5% of pregnancies. It is characterized by new-onset hypertension and proteinuria after 20 weeks of gestation. We investigated maternal second-trimester peripheral blood gene expression profiles to identify potential biomarkers for predicting late-onset PE. We found significant associations between PE and several inflammatory and immunological pathways, including the JAK-STAT signaling, leukocyte transendothelial migration, systemic lupus erythematosus (SLE), and graft versus host disease (GVHD). Twelve candidate biomarkers were identified, with high predictive power (AUC 0.74-0.87) for late-onset PE. These biomarkers were also associated with various blood cell populations, particularly intermediate monocytes. Our study highlights the role of maternal immune dysregulation in PE and the potential of second-trimester blood RNA profiles in disease prediction.

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Publication Details

Journal
Scientific Reports
Published
2025-11-26
DOI
https://doi.org/10.1038/s41598-025-26323-3
Primary Topic
Pregnancy and preeclampsia studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Signs of immune dysregulation in second-trimester maternal blood RNA profiles in late-onset preeclampsia

Katri Räikkönen, Satu Wedenoja, Sini Ezer, Juho Wedenoja et al.
Scientific Reports
Pregnancy and preeclampsia studies
article

Signs of immune dysregulation in second-trimester maternal blood RNA profiles in late-onset preeclampsia

Katri Räikkönen, Satu Wedenoja, Sini Ezer, Juho Wedenoja, Shintaro Katayama, Yazgeldi Gamze, Juha Kere
article en

Abstract

Preeclampsia (PE) is a hypertensive disorder that affects 5% of pregnancies. It is characterized by new-onset hypertension and proteinuria after 20 weeks of gestation. We investigated maternal second-trimester peripheral blood gene expression profiles to identify potential biomarkers for predicting late-onset PE. We found significant associations between PE and several inflammatory and immunological pathways, including the JAK-STAT signaling, leukocyte transendothelial migration, systemic lupus erythematosus (SLE), and graft versus host disease (GVHD). Twelve candidate biomarkers were identified, with high predictive power (AUC 0.74-0.87) for late-onset PE. These biomarkers were also associated with various blood cell populations, particularly intermediate monocytes. Our study highlights the role of maternal immune dysregulation in PE and the potential of second-trimester blood RNA profiles in disease prediction.

Scientific ReportsVol. 15(1)
University of Helsinki (FI), Helsinki Institute of Physics (FI), Helsinki University Hospital (FI), Karolinska Institutet (SE), Integrated Cardio Metabolic Centre (SE), Institute for Molecular Medicine Finland (FI), Folkhälsans Forskningscentrum (FI)
Jane ja Aatos Erkon Säätiö, China Scholarship Council, Sigrid Juséliuksen Säätiö
Openalex Percentile: Top 53%
Pregnancy and preeclampsia studies
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