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Altered Cerebellar Biochemical Profiles in Infants Born Prematurely
This study aims to compare the cerebellar biochemical profiles in preterm (PT) infants evaluated at term equivalent age (TEA) and healthy full-term newborns using proton magnetic resonance spectroscopy ((1)H-MRS). We explore the associations between altered cerebellar metabolite profiles and brain i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557848/ https://www.ncbi.nlm.nih.gov/pubmed/28811513 http://dx.doi.org/10.1038/s41598-017-08195-4 |
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author | Brossard-Racine, Marie Murnick, Jonathan Bouyssi-Kobar, Marine Coulombe, Janie Chang, Taeun Limperopoulos, Catherine |
author_facet | Brossard-Racine, Marie Murnick, Jonathan Bouyssi-Kobar, Marine Coulombe, Janie Chang, Taeun Limperopoulos, Catherine |
author_sort | Brossard-Racine, Marie |
collection | PubMed |
description | This study aims to compare the cerebellar biochemical profiles in preterm (PT) infants evaluated at term equivalent age (TEA) and healthy full-term newborns using proton magnetic resonance spectroscopy ((1)H-MRS). We explore the associations between altered cerebellar metabolite profiles and brain injury topography, severity of injury, and prematurity-related clinical complications. We prospectively collected high quality (1)H-MRS in 59 premature infants born ≤32 weeks and 61 healthy full term controls. (1)H-MRS data were processed using LCModel software to calculate absolute metabolite concentration for N-acetyl-aspartate (NAA), choline (Cho) and creatine (Cr). PT infants had significantly lower cerebellar NAA (p < 0.025) and higher Cho (p < 0.001) at TEA when compared to healthy controls. Creatine was not different between the two groups. The presence of cerebellar injury was consistently associated with reduced concentrations for NAA, Cho, and Cr. Postnatal infection was negatively associated with NAA and Cr (p < 005), while cerebral cortical brain injury severity was inversely associated with both Cho and Cr (p < 0.01). We report for the first time that premature birth is associated with altered cerebellar metabolite profiles when compared to term born controls. Infection, cerebellar injury and supratentorial injury are important risk factors for impaired preterm cerebellar biochemistry. |
format | Online Article Text |
id | pubmed-5557848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55578482017-08-16 Altered Cerebellar Biochemical Profiles in Infants Born Prematurely Brossard-Racine, Marie Murnick, Jonathan Bouyssi-Kobar, Marine Coulombe, Janie Chang, Taeun Limperopoulos, Catherine Sci Rep Article This study aims to compare the cerebellar biochemical profiles in preterm (PT) infants evaluated at term equivalent age (TEA) and healthy full-term newborns using proton magnetic resonance spectroscopy ((1)H-MRS). We explore the associations between altered cerebellar metabolite profiles and brain injury topography, severity of injury, and prematurity-related clinical complications. We prospectively collected high quality (1)H-MRS in 59 premature infants born ≤32 weeks and 61 healthy full term controls. (1)H-MRS data were processed using LCModel software to calculate absolute metabolite concentration for N-acetyl-aspartate (NAA), choline (Cho) and creatine (Cr). PT infants had significantly lower cerebellar NAA (p < 0.025) and higher Cho (p < 0.001) at TEA when compared to healthy controls. Creatine was not different between the two groups. The presence of cerebellar injury was consistently associated with reduced concentrations for NAA, Cho, and Cr. Postnatal infection was negatively associated with NAA and Cr (p < 005), while cerebral cortical brain injury severity was inversely associated with both Cho and Cr (p < 0.01). We report for the first time that premature birth is associated with altered cerebellar metabolite profiles when compared to term born controls. Infection, cerebellar injury and supratentorial injury are important risk factors for impaired preterm cerebellar biochemistry. Nature Publishing Group UK 2017-08-15 /pmc/articles/PMC5557848/ /pubmed/28811513 http://dx.doi.org/10.1038/s41598-017-08195-4 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Brossard-Racine, Marie Murnick, Jonathan Bouyssi-Kobar, Marine Coulombe, Janie Chang, Taeun Limperopoulos, Catherine Altered Cerebellar Biochemical Profiles in Infants Born Prematurely |
title | Altered Cerebellar Biochemical Profiles in Infants Born Prematurely |
title_full | Altered Cerebellar Biochemical Profiles in Infants Born Prematurely |
title_fullStr | Altered Cerebellar Biochemical Profiles in Infants Born Prematurely |
title_full_unstemmed | Altered Cerebellar Biochemical Profiles in Infants Born Prematurely |
title_short | Altered Cerebellar Biochemical Profiles in Infants Born Prematurely |
title_sort | altered cerebellar biochemical profiles in infants born prematurely |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557848/ https://www.ncbi.nlm.nih.gov/pubmed/28811513 http://dx.doi.org/10.1038/s41598-017-08195-4 |
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