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Umbilical Cord Blood NOS1 as a Potential Biomarker of Neonatal Encephalopathy

BACKGROUND: There are no definitive markers to aid in diagnosis of neonatal encephalopathy (NE). The purpose of our study was (1) to identify and evaluate the utility of neuronal nitric oxide synthase (NOS1) in umbilical cord blood as a NE biomarker and (2) to identify the source of NOS1 in umbilica...

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Autores principales: Lei, Jun, Paules, Cristina, Nigrini, Elisabeth, Rosenzweig, Jason M., Bahabry, Rudhab, Farzin, Azadeh, Yang, Samuel, Northington, Frances J., Oros, Daniel, McKenney, Stephanie, Johnston, Michael V., Graham, Ernest M., Burd, Irina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466059/
https://www.ncbi.nlm.nih.gov/pubmed/28649562
http://dx.doi.org/10.3389/fped.2017.00112
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author Lei, Jun
Paules, Cristina
Nigrini, Elisabeth
Rosenzweig, Jason M.
Bahabry, Rudhab
Farzin, Azadeh
Yang, Samuel
Northington, Frances J.
Oros, Daniel
McKenney, Stephanie
Johnston, Michael V.
Graham, Ernest M.
Burd, Irina
author_facet Lei, Jun
Paules, Cristina
Nigrini, Elisabeth
Rosenzweig, Jason M.
Bahabry, Rudhab
Farzin, Azadeh
Yang, Samuel
Northington, Frances J.
Oros, Daniel
McKenney, Stephanie
Johnston, Michael V.
Graham, Ernest M.
Burd, Irina
author_sort Lei, Jun
collection PubMed
description BACKGROUND: There are no definitive markers to aid in diagnosis of neonatal encephalopathy (NE). The purpose of our study was (1) to identify and evaluate the utility of neuronal nitric oxide synthase (NOS1) in umbilical cord blood as a NE biomarker and (2) to identify the source of NOS1 in umbilical cord blood. METHODS: This was a nested case–control study of neonates >35 weeks of gestation. ELISA for NOS1 in umbilical cord blood was performed. Sources of NOS1 in umbilical cord were investigated by immunohistochemistry, western blot, ELISA, and quantitative PCR. Furthermore, umbilical cords of full-term neonates were subjected to 1% hypoxia ex vivo. RESULTS: NOS1 was present in umbilical cord blood and increased in NE cases compared with controls. NOS1 was expressed in endothelial cells of the umbilical cord vein, but not in artery or blood cells. In ex vivo experiments, hypoxia was associated with increased levels of NOS1 in venous endothelial cells of the umbilical cord as well as in ex vivo culture medium. CONCLUSION: This is the first study to investigate an early marker of NE. NOS1 is elevated with hypoxia, and further studies are needed to investigate it as a valuable tool for early diagnosis of neonatal brain injury.
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spelling pubmed-54660592017-06-23 Umbilical Cord Blood NOS1 as a Potential Biomarker of Neonatal Encephalopathy Lei, Jun Paules, Cristina Nigrini, Elisabeth Rosenzweig, Jason M. Bahabry, Rudhab Farzin, Azadeh Yang, Samuel Northington, Frances J. Oros, Daniel McKenney, Stephanie Johnston, Michael V. Graham, Ernest M. Burd, Irina Front Pediatr Pediatrics BACKGROUND: There are no definitive markers to aid in diagnosis of neonatal encephalopathy (NE). The purpose of our study was (1) to identify and evaluate the utility of neuronal nitric oxide synthase (NOS1) in umbilical cord blood as a NE biomarker and (2) to identify the source of NOS1 in umbilical cord blood. METHODS: This was a nested case–control study of neonates >35 weeks of gestation. ELISA for NOS1 in umbilical cord blood was performed. Sources of NOS1 in umbilical cord were investigated by immunohistochemistry, western blot, ELISA, and quantitative PCR. Furthermore, umbilical cords of full-term neonates were subjected to 1% hypoxia ex vivo. RESULTS: NOS1 was present in umbilical cord blood and increased in NE cases compared with controls. NOS1 was expressed in endothelial cells of the umbilical cord vein, but not in artery or blood cells. In ex vivo experiments, hypoxia was associated with increased levels of NOS1 in venous endothelial cells of the umbilical cord as well as in ex vivo culture medium. CONCLUSION: This is the first study to investigate an early marker of NE. NOS1 is elevated with hypoxia, and further studies are needed to investigate it as a valuable tool for early diagnosis of neonatal brain injury. Frontiers Media S.A. 2017-05-22 /pmc/articles/PMC5466059/ /pubmed/28649562 http://dx.doi.org/10.3389/fped.2017.00112 Text en Copyright © 2017 Lei, Paules, Nigrini, Rosenzweig, Bahabry, Farzin, Yang, Northington, Oros, McKenney, Johnston, Graham and Burd. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Lei, Jun
Paules, Cristina
Nigrini, Elisabeth
Rosenzweig, Jason M.
Bahabry, Rudhab
Farzin, Azadeh
Yang, Samuel
Northington, Frances J.
Oros, Daniel
McKenney, Stephanie
Johnston, Michael V.
Graham, Ernest M.
Burd, Irina
Umbilical Cord Blood NOS1 as a Potential Biomarker of Neonatal Encephalopathy
title Umbilical Cord Blood NOS1 as a Potential Biomarker of Neonatal Encephalopathy
title_full Umbilical Cord Blood NOS1 as a Potential Biomarker of Neonatal Encephalopathy
title_fullStr Umbilical Cord Blood NOS1 as a Potential Biomarker of Neonatal Encephalopathy
title_full_unstemmed Umbilical Cord Blood NOS1 as a Potential Biomarker of Neonatal Encephalopathy
title_short Umbilical Cord Blood NOS1 as a Potential Biomarker of Neonatal Encephalopathy
title_sort umbilical cord blood nos1 as a potential biomarker of neonatal encephalopathy
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466059/
https://www.ncbi.nlm.nih.gov/pubmed/28649562
http://dx.doi.org/10.3389/fped.2017.00112
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