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Altered brain metabolite concentration and delayed neurodevelopment in preterm neonates

BACKGROUND: A very-low-birth-weight (VLBW) preterm infants is associated with an increased risk of impaired neurodevelopmental outcomes. In this study, we investigated how neonatal brain metabolite concentrations changed with postmenstrual age and examined the relationship between changes in concent...

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Autores principales: Tomiyasu, Moyoko, Shibasaki, Jun, Kawaguchi, Hiroshi, Enokizono, Mikako, Toyoshima, Katsuaki, Obata, Takayuki, Aida, Noriko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770132/
https://www.ncbi.nlm.nih.gov/pubmed/33674742
http://dx.doi.org/10.1038/s41390-021-01398-6
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author Tomiyasu, Moyoko
Shibasaki, Jun
Kawaguchi, Hiroshi
Enokizono, Mikako
Toyoshima, Katsuaki
Obata, Takayuki
Aida, Noriko
author_facet Tomiyasu, Moyoko
Shibasaki, Jun
Kawaguchi, Hiroshi
Enokizono, Mikako
Toyoshima, Katsuaki
Obata, Takayuki
Aida, Noriko
author_sort Tomiyasu, Moyoko
collection PubMed
description BACKGROUND: A very-low-birth-weight (VLBW) preterm infants is associated with an increased risk of impaired neurodevelopmental outcomes. In this study, we investigated how neonatal brain metabolite concentrations changed with postmenstrual age and examined the relationship between changes in concentration (slopes) and neurodevelopmental level at 3–4 years. METHODS: We retrospectively examined 108 VLBW preterm infants who had brain single-voxel magnetic resonance spectroscopy at 34–42 weeks’ postmenstrual age. Neurodevelopment was assessed using a developmental test, and subjects were classified into four groups: developmental quotient <70, 70–84, 85–100, and >100. One-way analyses of covariance and multiple-comparison post hoc tests were used to compare slopes. RESULTS: We observed correlations between postmenstrual age and the concentrations of N-acetylaspartate and N-acetylaspartylglutamate (tNAA) (p < 0.001); creatine and phosphocreatine (p < 0.001); glutamate and glutamine (p < 0.001); and myo-inositol (p = 0.049) in the deep gray matter; and tNAA (p < 0.001) in the centrum semiovale. A significant interaction was noted among the tNAA slopes of the four groups in the deep gray matter (p = 0.022), and we found a significant difference between the <70 and 85–100 groups (post hoc, p = 0.024). CONCLUSIONS: In VLBW preterm infants, the slopes of tNAA concentrations (adjusted for postmenstrual age) were associated with lower developmental quotients at 3–4 years. IMPACT: In very-low-birth-weight preterm-born infants, a slower increase in tNAA brain concentration at term-equivalent age was associated with poorer developmental outcomes at 3–4 years. The increase in tNAA concentration in very-low-birth-weight infants was slower in poorer developmental outcomes, and changes in tNAA concentration appeared to be more critical than changes in tCho for predicting developmental delays. While tNAA/tCho ratios were previously used to examine the correlation with neurodevelopment at 1–2 years, we used brain metabolite concentrations.
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spelling pubmed-87701322022-02-04 Altered brain metabolite concentration and delayed neurodevelopment in preterm neonates Tomiyasu, Moyoko Shibasaki, Jun Kawaguchi, Hiroshi Enokizono, Mikako Toyoshima, Katsuaki Obata, Takayuki Aida, Noriko Pediatr Res Clinical Research Article BACKGROUND: A very-low-birth-weight (VLBW) preterm infants is associated with an increased risk of impaired neurodevelopmental outcomes. In this study, we investigated how neonatal brain metabolite concentrations changed with postmenstrual age and examined the relationship between changes in concentration (slopes) and neurodevelopmental level at 3–4 years. METHODS: We retrospectively examined 108 VLBW preterm infants who had brain single-voxel magnetic resonance spectroscopy at 34–42 weeks’ postmenstrual age. Neurodevelopment was assessed using a developmental test, and subjects were classified into four groups: developmental quotient <70, 70–84, 85–100, and >100. One-way analyses of covariance and multiple-comparison post hoc tests were used to compare slopes. RESULTS: We observed correlations between postmenstrual age and the concentrations of N-acetylaspartate and N-acetylaspartylglutamate (tNAA) (p < 0.001); creatine and phosphocreatine (p < 0.001); glutamate and glutamine (p < 0.001); and myo-inositol (p = 0.049) in the deep gray matter; and tNAA (p < 0.001) in the centrum semiovale. A significant interaction was noted among the tNAA slopes of the four groups in the deep gray matter (p = 0.022), and we found a significant difference between the <70 and 85–100 groups (post hoc, p = 0.024). CONCLUSIONS: In VLBW preterm infants, the slopes of tNAA concentrations (adjusted for postmenstrual age) were associated with lower developmental quotients at 3–4 years. IMPACT: In very-low-birth-weight preterm-born infants, a slower increase in tNAA brain concentration at term-equivalent age was associated with poorer developmental outcomes at 3–4 years. The increase in tNAA concentration in very-low-birth-weight infants was slower in poorer developmental outcomes, and changes in tNAA concentration appeared to be more critical than changes in tCho for predicting developmental delays. While tNAA/tCho ratios were previously used to examine the correlation with neurodevelopment at 1–2 years, we used brain metabolite concentrations. Nature Publishing Group US 2021-03-05 2022 /pmc/articles/PMC8770132/ /pubmed/33674742 http://dx.doi.org/10.1038/s41390-021-01398-6 Text en © The Author(s) 2021 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 Clinical Research Article
Tomiyasu, Moyoko
Shibasaki, Jun
Kawaguchi, Hiroshi
Enokizono, Mikako
Toyoshima, Katsuaki
Obata, Takayuki
Aida, Noriko
Altered brain metabolite concentration and delayed neurodevelopment in preterm neonates
title Altered brain metabolite concentration and delayed neurodevelopment in preterm neonates
title_full Altered brain metabolite concentration and delayed neurodevelopment in preterm neonates
title_fullStr Altered brain metabolite concentration and delayed neurodevelopment in preterm neonates
title_full_unstemmed Altered brain metabolite concentration and delayed neurodevelopment in preterm neonates
title_short Altered brain metabolite concentration and delayed neurodevelopment in preterm neonates
title_sort altered brain metabolite concentration and delayed neurodevelopment in preterm neonates
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770132/
https://www.ncbi.nlm.nih.gov/pubmed/33674742
http://dx.doi.org/10.1038/s41390-021-01398-6
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