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Serum brain injury biomarkers are gestationally and post-natally regulated in non-brain injured neonates

OBJECTIVE: To determine the association of gestational age (GA) and day of life (DOL) with the circulating serum concentration of six brain injury-associated biomarkers in non-brain injured neonates born between 23–41 weeks’ GA. METHODS: In a multicenter prospective observational cohort study, serum...

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Autores principales: Brooks, Sandra, Friedes, Barbara D, Northington, Frances, Graham, Ernest, Tekes, Aylin, Burton, Vera J, Gerner, Gwendolyn, Zhu, Jie, Chavez-Valdez, Raul, Vaidya, Dhananjay, Everett, Allen D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206041/
https://www.ncbi.nlm.nih.gov/pubmed/34923579
http://dx.doi.org/10.1038/s41390-021-01906-8
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author Brooks, Sandra
Friedes, Barbara D
Northington, Frances
Graham, Ernest
Tekes, Aylin
Burton, Vera J
Gerner, Gwendolyn
Zhu, Jie
Chavez-Valdez, Raul
Vaidya, Dhananjay
Everett, Allen D
author_facet Brooks, Sandra
Friedes, Barbara D
Northington, Frances
Graham, Ernest
Tekes, Aylin
Burton, Vera J
Gerner, Gwendolyn
Zhu, Jie
Chavez-Valdez, Raul
Vaidya, Dhananjay
Everett, Allen D
author_sort Brooks, Sandra
collection PubMed
description OBJECTIVE: To determine the association of gestational age (GA) and day of life (DOL) with the circulating serum concentration of six brain injury-associated biomarkers in non-brain injured neonates born between 23–41 weeks’ GA. METHODS: In a multicenter prospective observational cohort study, serum CNS-insult, inflammatory and trophic proteins concentrations were measured daily in the first 7 DOL. RESULTS: 3232 serum samples were analyzed from 745 enrollees, median GA 32.3 weeks. BDNF increased 3.7% and IL-8 increased 8.9% each week of gestation. VEGF, IL-6, and IL-10 showed no relationship with GA. VEGF increased 10.8% and IL-8 18.9%, each DOL. IL-6 decreased by 15.8% each DOL. IL-10 decreased by 81.4% each DOL for DOL 0–3. BDNF did not change with DOL. Only 49.67% of samples had detectable GFAP and 33.15% had detectable NRGN. The odds of having detectable GFAP and NRGN increased by 53% and 11%, respectively, each week after 36 weeks’ GA. The odds of having detectable GFAP and NRGN decreased by 15% and 8%, respectively, each DOL. CONCLUSION: BDNF and IL-8 serum concentrations vary with GA. VEGF and interleukin concentrations are dynamic in the first week of life, suggesting circulating levels should be adjusted for GA and DOL for clinically relevant assessment of brain injury.
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spelling pubmed-92060412023-06-18 Serum brain injury biomarkers are gestationally and post-natally regulated in non-brain injured neonates Brooks, Sandra Friedes, Barbara D Northington, Frances Graham, Ernest Tekes, Aylin Burton, Vera J Gerner, Gwendolyn Zhu, Jie Chavez-Valdez, Raul Vaidya, Dhananjay Everett, Allen D Pediatr Res Article OBJECTIVE: To determine the association of gestational age (GA) and day of life (DOL) with the circulating serum concentration of six brain injury-associated biomarkers in non-brain injured neonates born between 23–41 weeks’ GA. METHODS: In a multicenter prospective observational cohort study, serum CNS-insult, inflammatory and trophic proteins concentrations were measured daily in the first 7 DOL. RESULTS: 3232 serum samples were analyzed from 745 enrollees, median GA 32.3 weeks. BDNF increased 3.7% and IL-8 increased 8.9% each week of gestation. VEGF, IL-6, and IL-10 showed no relationship with GA. VEGF increased 10.8% and IL-8 18.9%, each DOL. IL-6 decreased by 15.8% each DOL. IL-10 decreased by 81.4% each DOL for DOL 0–3. BDNF did not change with DOL. Only 49.67% of samples had detectable GFAP and 33.15% had detectable NRGN. The odds of having detectable GFAP and NRGN increased by 53% and 11%, respectively, each week after 36 weeks’ GA. The odds of having detectable GFAP and NRGN decreased by 15% and 8%, respectively, each DOL. CONCLUSION: BDNF and IL-8 serum concentrations vary with GA. VEGF and interleukin concentrations are dynamic in the first week of life, suggesting circulating levels should be adjusted for GA and DOL for clinically relevant assessment of brain injury. 2023-06 2021-12-18 /pmc/articles/PMC9206041/ /pubmed/34923579 http://dx.doi.org/10.1038/s41390-021-01906-8 Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Brooks, Sandra
Friedes, Barbara D
Northington, Frances
Graham, Ernest
Tekes, Aylin
Burton, Vera J
Gerner, Gwendolyn
Zhu, Jie
Chavez-Valdez, Raul
Vaidya, Dhananjay
Everett, Allen D
Serum brain injury biomarkers are gestationally and post-natally regulated in non-brain injured neonates
title Serum brain injury biomarkers are gestationally and post-natally regulated in non-brain injured neonates
title_full Serum brain injury biomarkers are gestationally and post-natally regulated in non-brain injured neonates
title_fullStr Serum brain injury biomarkers are gestationally and post-natally regulated in non-brain injured neonates
title_full_unstemmed Serum brain injury biomarkers are gestationally and post-natally regulated in non-brain injured neonates
title_short Serum brain injury biomarkers are gestationally and post-natally regulated in non-brain injured neonates
title_sort serum brain injury biomarkers are gestationally and post-natally regulated in non-brain injured neonates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206041/
https://www.ncbi.nlm.nih.gov/pubmed/34923579
http://dx.doi.org/10.1038/s41390-021-01906-8
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