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Neonatal Autonomic Function After Pregnancy Complications and Early Cardiovascular Development
BACKGROUND: Heart rate variability (HRV) has emerged as a predictor of later cardiac risk. This study tested whether pregnancy complications that may have long-term offspring cardiac sequelae are associated with differences in HRV at birth, and whether these HRV differences identify abnormal cardiov...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086328/ https://www.ncbi.nlm.nih.gov/pubmed/29795212 http://dx.doi.org/10.1038/s41390-018-0021-0 |
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author | Aye, Christina YL Lewandowski, Adam James Oster, Julien Upton, Ross Davis, Esther Kenworthy, Yvonne Boardman, Henry Yu, Grace Z Siepmann, Timo Adwani, Satish McCormick, Kenny Sverrisdottir, Yrsa B Leeson, Paul |
author_facet | Aye, Christina YL Lewandowski, Adam James Oster, Julien Upton, Ross Davis, Esther Kenworthy, Yvonne Boardman, Henry Yu, Grace Z Siepmann, Timo Adwani, Satish McCormick, Kenny Sverrisdottir, Yrsa B Leeson, Paul |
author_sort | Aye, Christina YL |
collection | PubMed |
description | BACKGROUND: Heart rate variability (HRV) has emerged as a predictor of later cardiac risk. This study tested whether pregnancy complications that may have long-term offspring cardiac sequelae are associated with differences in HRV at birth, and whether these HRV differences identify abnormal cardiovascular development in the postnatal period. METHODS: 98 sleeping neonates had 5-minute electrocardiogram recordings at birth. Standard time and frequency domain parameters were calculated and related to cardiovascular measures at birth and three months of age. RESULTS: Increasing prematurity, but not maternal hypertension or growth restriction, was associated with decreased HRV at birth as demonstrated by a lower root mean square of the difference between adjacent NN intervals (rMSSD), low (LF) and high frequency power (HF) with decreasing gestational age (p<0.001, p=0.009 and p=0.007 respectively). We also demonstrated a relative imbalance between sympathetic and parasympathetic tone compared to term infants. However, differences in autonomic function did not predict cardiovascular measures at either time-point. CONCLUSIONS: Altered cardiac autonomic function at birth relates to prematurity rather than other pregnancy complications and does not predict cardiovascular developmental patterns during the first three months post birth. Long-term studies will be needed to understand relevance to cardiovascular risk. |
format | Online Article Text |
id | pubmed-6086328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-60863282018-11-23 Neonatal Autonomic Function After Pregnancy Complications and Early Cardiovascular Development Aye, Christina YL Lewandowski, Adam James Oster, Julien Upton, Ross Davis, Esther Kenworthy, Yvonne Boardman, Henry Yu, Grace Z Siepmann, Timo Adwani, Satish McCormick, Kenny Sverrisdottir, Yrsa B Leeson, Paul Pediatr Res Article BACKGROUND: Heart rate variability (HRV) has emerged as a predictor of later cardiac risk. This study tested whether pregnancy complications that may have long-term offspring cardiac sequelae are associated with differences in HRV at birth, and whether these HRV differences identify abnormal cardiovascular development in the postnatal period. METHODS: 98 sleeping neonates had 5-minute electrocardiogram recordings at birth. Standard time and frequency domain parameters were calculated and related to cardiovascular measures at birth and three months of age. RESULTS: Increasing prematurity, but not maternal hypertension or growth restriction, was associated with decreased HRV at birth as demonstrated by a lower root mean square of the difference between adjacent NN intervals (rMSSD), low (LF) and high frequency power (HF) with decreasing gestational age (p<0.001, p=0.009 and p=0.007 respectively). We also demonstrated a relative imbalance between sympathetic and parasympathetic tone compared to term infants. However, differences in autonomic function did not predict cardiovascular measures at either time-point. CONCLUSIONS: Altered cardiac autonomic function at birth relates to prematurity rather than other pregnancy complications and does not predict cardiovascular developmental patterns during the first three months post birth. Long-term studies will be needed to understand relevance to cardiovascular risk. 2018-05-23 2018-07 /pmc/articles/PMC6086328/ /pubmed/29795212 http://dx.doi.org/10.1038/s41390-018-0021-0 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users 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 Aye, Christina YL Lewandowski, Adam James Oster, Julien Upton, Ross Davis, Esther Kenworthy, Yvonne Boardman, Henry Yu, Grace Z Siepmann, Timo Adwani, Satish McCormick, Kenny Sverrisdottir, Yrsa B Leeson, Paul Neonatal Autonomic Function After Pregnancy Complications and Early Cardiovascular Development |
title | Neonatal Autonomic Function After Pregnancy Complications and Early Cardiovascular Development |
title_full | Neonatal Autonomic Function After Pregnancy Complications and Early Cardiovascular Development |
title_fullStr | Neonatal Autonomic Function After Pregnancy Complications and Early Cardiovascular Development |
title_full_unstemmed | Neonatal Autonomic Function After Pregnancy Complications and Early Cardiovascular Development |
title_short | Neonatal Autonomic Function After Pregnancy Complications and Early Cardiovascular Development |
title_sort | neonatal autonomic function after pregnancy complications and early cardiovascular development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086328/ https://www.ncbi.nlm.nih.gov/pubmed/29795212 http://dx.doi.org/10.1038/s41390-018-0021-0 |
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