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Heart rate variability and inflammatory markers in neonates with hypoxic‐ischemic encephalopathy
To examine heart rate variability (HRV) and inflammatory markers as predictors for neurological injury in neonates undergoing therapeutic hypothermia for hypoxic‐ischemic encephalopathy (HIE). We hypothesized that HRV would differentiate between infants with no/mild injury and infants with moderate/...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687857/ https://www.ncbi.nlm.nih.gov/pubmed/31397094 http://dx.doi.org/10.14814/phy2.14110 |
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author | Yasova Barbeau, Daphna Krueger, Charlene Huene, Melissa Copenhaver, Nicole Bennett, Jeffrey Weaver, Michael Weiss, Michael D. |
author_facet | Yasova Barbeau, Daphna Krueger, Charlene Huene, Melissa Copenhaver, Nicole Bennett, Jeffrey Weaver, Michael Weiss, Michael D. |
author_sort | Yasova Barbeau, Daphna |
collection | PubMed |
description | To examine heart rate variability (HRV) and inflammatory markers as predictors for neurological injury in neonates undergoing therapeutic hypothermia for hypoxic‐ischemic encephalopathy (HIE). We hypothesized that HRV would differentiate between infants with no/mild injury and infants with moderate/severe injury observed on MRI. Because HRV can be associated with the inflammatory cascade, cytokine concentrations were compared with the severity of brain injury indicated by MRI. Further, we studied the effect of temperature, sex, and mechanical ventilation on HRV. HRV was prospectively collected on neonates with HIE using spectral analysis for low and high frequency components (n = 16). A subset (n = 10) of neonates had serum available for inflammatory cytokine analysis obtained during cooling. Neonates were stratified into no/mild or moderate/severe injury based on MRI obtained after rewarming. Differences in HRV were identified; lower low frequency power predicted more injury on MRI. Additionally, in neonates with HIE after cooling procedure, HRV differed by gender. Elevated RANTES (CCL5) and decreased GM‐CSF (Granulocyte‐macrophage colony‐stimulating factor) at 96 hours predicted less severe injury. In this small study, HRV differs between no/mild and moderate/severe injury in neonates with HIE. With further study, this may aid the clinician in real‐time decision making. HRV differs by gender. Finally, inflammatory biomarkers may help elucidate the pathophysiology of HIE. |
format | Online Article Text |
id | pubmed-6687857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66878572019-08-14 Heart rate variability and inflammatory markers in neonates with hypoxic‐ischemic encephalopathy Yasova Barbeau, Daphna Krueger, Charlene Huene, Melissa Copenhaver, Nicole Bennett, Jeffrey Weaver, Michael Weiss, Michael D. Physiol Rep Original Research To examine heart rate variability (HRV) and inflammatory markers as predictors for neurological injury in neonates undergoing therapeutic hypothermia for hypoxic‐ischemic encephalopathy (HIE). We hypothesized that HRV would differentiate between infants with no/mild injury and infants with moderate/severe injury observed on MRI. Because HRV can be associated with the inflammatory cascade, cytokine concentrations were compared with the severity of brain injury indicated by MRI. Further, we studied the effect of temperature, sex, and mechanical ventilation on HRV. HRV was prospectively collected on neonates with HIE using spectral analysis for low and high frequency components (n = 16). A subset (n = 10) of neonates had serum available for inflammatory cytokine analysis obtained during cooling. Neonates were stratified into no/mild or moderate/severe injury based on MRI obtained after rewarming. Differences in HRV were identified; lower low frequency power predicted more injury on MRI. Additionally, in neonates with HIE after cooling procedure, HRV differed by gender. Elevated RANTES (CCL5) and decreased GM‐CSF (Granulocyte‐macrophage colony‐stimulating factor) at 96 hours predicted less severe injury. In this small study, HRV differs between no/mild and moderate/severe injury in neonates with HIE. With further study, this may aid the clinician in real‐time decision making. HRV differs by gender. Finally, inflammatory biomarkers may help elucidate the pathophysiology of HIE. John Wiley and Sons Inc. 2019-08-08 /pmc/articles/PMC6687857/ /pubmed/31397094 http://dx.doi.org/10.14814/phy2.14110 Text en © 2019 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Yasova Barbeau, Daphna Krueger, Charlene Huene, Melissa Copenhaver, Nicole Bennett, Jeffrey Weaver, Michael Weiss, Michael D. Heart rate variability and inflammatory markers in neonates with hypoxic‐ischemic encephalopathy |
title | Heart rate variability and inflammatory markers in neonates with hypoxic‐ischemic encephalopathy |
title_full | Heart rate variability and inflammatory markers in neonates with hypoxic‐ischemic encephalopathy |
title_fullStr | Heart rate variability and inflammatory markers in neonates with hypoxic‐ischemic encephalopathy |
title_full_unstemmed | Heart rate variability and inflammatory markers in neonates with hypoxic‐ischemic encephalopathy |
title_short | Heart rate variability and inflammatory markers in neonates with hypoxic‐ischemic encephalopathy |
title_sort | heart rate variability and inflammatory markers in neonates with hypoxic‐ischemic encephalopathy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687857/ https://www.ncbi.nlm.nih.gov/pubmed/31397094 http://dx.doi.org/10.14814/phy2.14110 |
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