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The umbilical cord, preeclampsia and the VEGF family

INTRODUCTION: The VEGF family has been identified as abnormal in preeclampsia (PE). Hypertensive disorders of pregnancy (HDP) are major contributors to maternal and neonatal morbidity and mortality worldwide; likewise, umbilical cord anatomical abnormalities (UCAA) are linked to poor neonatal outcom...

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Autores principales: Olaya-C, Mercedes, Garrido, Marta, Hernandez-Losa, Javier, Sesé, Marta, Ayala-Ramirez, Paola, Somoza, Rosa, Vargas, Magda Jimena, Ramón y Cajal, Santiago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276640/
https://www.ncbi.nlm.nih.gov/pubmed/30568515
http://dx.doi.org/10.2147/IJWH.S174734
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author Olaya-C, Mercedes
Garrido, Marta
Hernandez-Losa, Javier
Sesé, Marta
Ayala-Ramirez, Paola
Somoza, Rosa
Vargas, Magda Jimena
Ramón y Cajal, Santiago
author_facet Olaya-C, Mercedes
Garrido, Marta
Hernandez-Losa, Javier
Sesé, Marta
Ayala-Ramirez, Paola
Somoza, Rosa
Vargas, Magda Jimena
Ramón y Cajal, Santiago
author_sort Olaya-C, Mercedes
collection PubMed
description INTRODUCTION: The VEGF family has been identified as abnormal in preeclampsia (PE). Hypertensive disorders of pregnancy (HDP) are major contributors to maternal and neonatal morbidity and mortality worldwide; likewise, umbilical cord anatomical abnormalities (UCAA) are linked to poor neonatal outcomes. Based on the relationship described between PE and UCAA and the role of the VEGF family in PE, this study explored VEGF expression in placental and UC tissued from patients with PE and with UCAA. METHODS: We performed an observational, analytical study on placentas, comparing protein and mRNA expression in four groups: patients with PE, patients with UC abnormalities, patients with both, and patients with none of them. Using immunohistochemistry, we studied VEGF A, VEGF R1 (FLT1), MMP1, and PLGF. With quantitative reverse transcription polymerase chain reaction we described mRNA expression of PLGF, VEGF and sFLT1, and sFLT1/PLGF ratio. RESULTS: Forty newborns were included. Sixty-seven percent of mothers and 45% of newborns developed no complications. Immunohistochemistry was performed on UC and placental disc paraffin-embedded tissue; in the latter, the mRNA of the VEGF family was also measured. Statistically significant differences were observed among different expressions in both HDP and UCAA groups. Interestingly, the UCAA group exhibited lower levels of sFLT1 and VEGF-A in comparison with other groups, with significant P-value for sFLT1 (P=0000.1). CONCLUSION: The origin of UCAA abnormalities and their relation with HDP are still unknown. VEGF family alterations could be involved in both. This study provides the first approach related to molecules linked to UCAA.
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spelling pubmed-62766402018-12-19 The umbilical cord, preeclampsia and the VEGF family Olaya-C, Mercedes Garrido, Marta Hernandez-Losa, Javier Sesé, Marta Ayala-Ramirez, Paola Somoza, Rosa Vargas, Magda Jimena Ramón y Cajal, Santiago Int J Womens Health Original Research INTRODUCTION: The VEGF family has been identified as abnormal in preeclampsia (PE). Hypertensive disorders of pregnancy (HDP) are major contributors to maternal and neonatal morbidity and mortality worldwide; likewise, umbilical cord anatomical abnormalities (UCAA) are linked to poor neonatal outcomes. Based on the relationship described between PE and UCAA and the role of the VEGF family in PE, this study explored VEGF expression in placental and UC tissued from patients with PE and with UCAA. METHODS: We performed an observational, analytical study on placentas, comparing protein and mRNA expression in four groups: patients with PE, patients with UC abnormalities, patients with both, and patients with none of them. Using immunohistochemistry, we studied VEGF A, VEGF R1 (FLT1), MMP1, and PLGF. With quantitative reverse transcription polymerase chain reaction we described mRNA expression of PLGF, VEGF and sFLT1, and sFLT1/PLGF ratio. RESULTS: Forty newborns were included. Sixty-seven percent of mothers and 45% of newborns developed no complications. Immunohistochemistry was performed on UC and placental disc paraffin-embedded tissue; in the latter, the mRNA of the VEGF family was also measured. Statistically significant differences were observed among different expressions in both HDP and UCAA groups. Interestingly, the UCAA group exhibited lower levels of sFLT1 and VEGF-A in comparison with other groups, with significant P-value for sFLT1 (P=0000.1). CONCLUSION: The origin of UCAA abnormalities and their relation with HDP are still unknown. VEGF family alterations could be involved in both. This study provides the first approach related to molecules linked to UCAA. Dove Medical Press 2018-11-28 /pmc/articles/PMC6276640/ /pubmed/30568515 http://dx.doi.org/10.2147/IJWH.S174734 Text en © 2018 Olaya-C et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Olaya-C, Mercedes
Garrido, Marta
Hernandez-Losa, Javier
Sesé, Marta
Ayala-Ramirez, Paola
Somoza, Rosa
Vargas, Magda Jimena
Ramón y Cajal, Santiago
The umbilical cord, preeclampsia and the VEGF family
title The umbilical cord, preeclampsia and the VEGF family
title_full The umbilical cord, preeclampsia and the VEGF family
title_fullStr The umbilical cord, preeclampsia and the VEGF family
title_full_unstemmed The umbilical cord, preeclampsia and the VEGF family
title_short The umbilical cord, preeclampsia and the VEGF family
title_sort umbilical cord, preeclampsia and the vegf family
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276640/
https://www.ncbi.nlm.nih.gov/pubmed/30568515
http://dx.doi.org/10.2147/IJWH.S174734
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