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Early-pregnancy transcriptome signatures of preeclampsia: from peripheral blood to placenta

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, m...

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Autores principales: Yadama, Aishwarya P., Maiorino, Enrico, Carey, Vincent J., McElrath, Thomas F., Litonjua, Augusto A., Loscalzo, Joseph, Weiss, Scott T., Mirzakhani, Hooman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550614/
https://www.ncbi.nlm.nih.gov/pubmed/33046794
http://dx.doi.org/10.1038/s41598-020-74100-1
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author Yadama, Aishwarya P.
Maiorino, Enrico
Carey, Vincent J.
McElrath, Thomas F.
Litonjua, Augusto A.
Loscalzo, Joseph
Weiss, Scott T.
Mirzakhani, Hooman
author_facet Yadama, Aishwarya P.
Maiorino, Enrico
Carey, Vincent J.
McElrath, Thomas F.
Litonjua, Augusto A.
Loscalzo, Joseph
Weiss, Scott T.
Mirzakhani, Hooman
author_sort Yadama, Aishwarya P.
collection PubMed
description 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.
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spelling pubmed-75506142020-10-14 Early-pregnancy transcriptome signatures of preeclampsia: from peripheral blood to placenta Yadama, Aishwarya P. Maiorino, Enrico Carey, Vincent J. McElrath, Thomas F. Litonjua, Augusto A. Loscalzo, Joseph Weiss, Scott T. Mirzakhani, Hooman Sci Rep Article 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. Nature Publishing Group UK 2020-10-12 /pmc/articles/PMC7550614/ /pubmed/33046794 http://dx.doi.org/10.1038/s41598-020-74100-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yadama, Aishwarya P.
Maiorino, Enrico
Carey, Vincent J.
McElrath, Thomas F.
Litonjua, Augusto A.
Loscalzo, Joseph
Weiss, Scott T.
Mirzakhani, Hooman
Early-pregnancy transcriptome signatures of preeclampsia: from peripheral blood to placenta
title Early-pregnancy transcriptome signatures of preeclampsia: from peripheral blood to placenta
title_full Early-pregnancy transcriptome signatures of preeclampsia: from peripheral blood to placenta
title_fullStr Early-pregnancy transcriptome signatures of preeclampsia: from peripheral blood to placenta
title_full_unstemmed Early-pregnancy transcriptome signatures of preeclampsia: from peripheral blood to placenta
title_short Early-pregnancy transcriptome signatures of preeclampsia: from peripheral blood to placenta
title_sort early-pregnancy transcriptome signatures of preeclampsia: from peripheral blood to placenta
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550614/
https://www.ncbi.nlm.nih.gov/pubmed/33046794
http://dx.doi.org/10.1038/s41598-020-74100-1
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