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Electroencephalographic studies in growth-restricted and small-for-gestational-age neonates

ABSTRACT: Foetal growth restriction (FGR) and being born small for gestational age (SGA) are associated with neurodevelopmental delay. Early diagnosis of neurological damage is difficult in FGR and SGA neonates. Electroencephalography (EEG) has the potential as a tool for the assessment of brain dev...

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Autores principales: Stevenson, Nathan J., Lai, Melissa M., Starkman, Hava E., Colditz, Paul B., Wixey, Julie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771813/
https://www.ncbi.nlm.nih.gov/pubmed/35197567
http://dx.doi.org/10.1038/s41390-022-01992-2
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author Stevenson, Nathan J.
Lai, Melissa M.
Starkman, Hava E.
Colditz, Paul B.
Wixey, Julie A.
author_facet Stevenson, Nathan J.
Lai, Melissa M.
Starkman, Hava E.
Colditz, Paul B.
Wixey, Julie A.
author_sort Stevenson, Nathan J.
collection PubMed
description ABSTRACT: Foetal growth restriction (FGR) and being born small for gestational age (SGA) are associated with neurodevelopmental delay. Early diagnosis of neurological damage is difficult in FGR and SGA neonates. Electroencephalography (EEG) has the potential as a tool for the assessment of brain development in FGR/SGA neonates. In this review, we analyse the evidence base on the use of EEG for the assessment of neonates with FGR or SGA. We found consistent findings that FGR/SGA is associated with measurable changes in the EEG that present immediately after birth and persist into childhood. Early manifestations of FGR/SGA in the EEG include changes in spectral power, symmetry/synchrony, sleep–wake cycling, and the continuity of EEG amplitude. Later manifestations of FGR/SGA into infancy and early childhood include changes in spectral power, sleep architecture, and EEG amplitude. FGR/SGA infants had poorer neurodevelopmental outcomes than appropriate for gestational age controls. The EEG has the potential to identify FGR/SGA infants and assess the functional correlates of neurological damage. IMPACT: FGR/SGA neonates have significantly different EEG activity compared to AGA neonates. EEG differences persist into childhood and are associated with adverse neurodevelopmental outcomes. EEG has the potential for early identification of brain impairment in FGR/SGA neonates.
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spelling pubmed-97718132022-12-23 Electroencephalographic studies in growth-restricted and small-for-gestational-age neonates Stevenson, Nathan J. Lai, Melissa M. Starkman, Hava E. Colditz, Paul B. Wixey, Julie A. Pediatr Res Review Article ABSTRACT: Foetal growth restriction (FGR) and being born small for gestational age (SGA) are associated with neurodevelopmental delay. Early diagnosis of neurological damage is difficult in FGR and SGA neonates. Electroencephalography (EEG) has the potential as a tool for the assessment of brain development in FGR/SGA neonates. In this review, we analyse the evidence base on the use of EEG for the assessment of neonates with FGR or SGA. We found consistent findings that FGR/SGA is associated with measurable changes in the EEG that present immediately after birth and persist into childhood. Early manifestations of FGR/SGA in the EEG include changes in spectral power, symmetry/synchrony, sleep–wake cycling, and the continuity of EEG amplitude. Later manifestations of FGR/SGA into infancy and early childhood include changes in spectral power, sleep architecture, and EEG amplitude. FGR/SGA infants had poorer neurodevelopmental outcomes than appropriate for gestational age controls. The EEG has the potential to identify FGR/SGA infants and assess the functional correlates of neurological damage. IMPACT: FGR/SGA neonates have significantly different EEG activity compared to AGA neonates. EEG differences persist into childhood and are associated with adverse neurodevelopmental outcomes. EEG has the potential for early identification of brain impairment in FGR/SGA neonates. Nature Publishing Group US 2022-02-23 2022 /pmc/articles/PMC9771813/ /pubmed/35197567 http://dx.doi.org/10.1038/s41390-022-01992-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Stevenson, Nathan J.
Lai, Melissa M.
Starkman, Hava E.
Colditz, Paul B.
Wixey, Julie A.
Electroencephalographic studies in growth-restricted and small-for-gestational-age neonates
title Electroencephalographic studies in growth-restricted and small-for-gestational-age neonates
title_full Electroencephalographic studies in growth-restricted and small-for-gestational-age neonates
title_fullStr Electroencephalographic studies in growth-restricted and small-for-gestational-age neonates
title_full_unstemmed Electroencephalographic studies in growth-restricted and small-for-gestational-age neonates
title_short Electroencephalographic studies in growth-restricted and small-for-gestational-age neonates
title_sort electroencephalographic studies in growth-restricted and small-for-gestational-age neonates
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771813/
https://www.ncbi.nlm.nih.gov/pubmed/35197567
http://dx.doi.org/10.1038/s41390-022-01992-2
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