Cargando…

Neurometabolic changes in neonates with congenital heart defects and their relation to neurodevelopmental outcome

BACKGROUND: Altered neurometabolite ratios in neonates undergoing cardiac surgery for congenital heart defects (CHD) may serve as a biomarker for altered brain development and neurodevelopment (ND). METHODS: We analyzed single voxel 3T PRESS H(1)-MRS data, acquired unilaterally in the left basal gan...

Descripción completa

Detalles Bibliográficos
Autores principales: Steger, Céline, Feldmann, Maria, Borns, Julia, Hagmann, Cornelia, Latal, Beatrice, Held, Ulrike, Jakab, András, O’Gorman Tuura, Ruth, Knirsch, Walter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172141/
https://www.ncbi.nlm.nih.gov/pubmed/35995938
http://dx.doi.org/10.1038/s41390-022-02253-y
_version_ 1785039560256782336
author Steger, Céline
Feldmann, Maria
Borns, Julia
Hagmann, Cornelia
Latal, Beatrice
Held, Ulrike
Jakab, András
O’Gorman Tuura, Ruth
Knirsch, Walter
author_facet Steger, Céline
Feldmann, Maria
Borns, Julia
Hagmann, Cornelia
Latal, Beatrice
Held, Ulrike
Jakab, András
O’Gorman Tuura, Ruth
Knirsch, Walter
author_sort Steger, Céline
collection PubMed
description BACKGROUND: Altered neurometabolite ratios in neonates undergoing cardiac surgery for congenital heart defects (CHD) may serve as a biomarker for altered brain development and neurodevelopment (ND). METHODS: We analyzed single voxel 3T PRESS H(1)-MRS data, acquired unilaterally in the left basal ganglia and white matter of 88 CHD neonates before and/or after neonatal cardiac surgery and 30 healthy controls. Metabolite ratios to Creatine (Cr) included glutamate (Glu/Cr), myo-Inositol (mI/Cr), glutamate and glutamine (Glx/Cr), and lactate (Lac/Cr). In addition, the developmental marker N-acetylaspartate to choline (NAA/Cho) was evaluated. All children underwent ND outcome testing using the Bayley Scales of Infant and Toddler Development Third Edition (BSID-III) at 1 year of age. RESULTS: White matter NAA/Cho ratios were lower in CHD neonates compared to healthy controls (group beta estimate: −0.26, std. error 0.07, 95% CI: −0.40 – 0.13, p value <0.001, FDR corrected p value = 0.010). We found no correlation between pre- or postoperative white matter NAA/Cho with ND outcome while controlling for socioeconomic status and CHD diagnosis. CONCLUSION: Reduced white matter NAA/Cho in CHD neonates undergoing cardiac surgery may reflect a delay in brain maturation. Further long-term MRS studies are needed to improve our understanding of the clinical impact of altered metabolites on brain development and outcome. IMPACT: NAA/Cho was reduced in the white matter, but not the gray matter of CHD neonates compared to healthy controls. No correlation to the 1-year neurodevelopmental outcome (Bayley-III) was found. While the rapid change of NAA/Cho with age might make it a sensitive marker for a delay in brain maturation, the relationship to neurodevelopmental outcome requires further investigation.
format Online
Article
Text
id pubmed-10172141
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group US
record_format MEDLINE/PubMed
spelling pubmed-101721412023-05-12 Neurometabolic changes in neonates with congenital heart defects and their relation to neurodevelopmental outcome Steger, Céline Feldmann, Maria Borns, Julia Hagmann, Cornelia Latal, Beatrice Held, Ulrike Jakab, András O’Gorman Tuura, Ruth Knirsch, Walter Pediatr Res Clinical Research Article BACKGROUND: Altered neurometabolite ratios in neonates undergoing cardiac surgery for congenital heart defects (CHD) may serve as a biomarker for altered brain development and neurodevelopment (ND). METHODS: We analyzed single voxel 3T PRESS H(1)-MRS data, acquired unilaterally in the left basal ganglia and white matter of 88 CHD neonates before and/or after neonatal cardiac surgery and 30 healthy controls. Metabolite ratios to Creatine (Cr) included glutamate (Glu/Cr), myo-Inositol (mI/Cr), glutamate and glutamine (Glx/Cr), and lactate (Lac/Cr). In addition, the developmental marker N-acetylaspartate to choline (NAA/Cho) was evaluated. All children underwent ND outcome testing using the Bayley Scales of Infant and Toddler Development Third Edition (BSID-III) at 1 year of age. RESULTS: White matter NAA/Cho ratios were lower in CHD neonates compared to healthy controls (group beta estimate: −0.26, std. error 0.07, 95% CI: −0.40 – 0.13, p value <0.001, FDR corrected p value = 0.010). We found no correlation between pre- or postoperative white matter NAA/Cho with ND outcome while controlling for socioeconomic status and CHD diagnosis. CONCLUSION: Reduced white matter NAA/Cho in CHD neonates undergoing cardiac surgery may reflect a delay in brain maturation. Further long-term MRS studies are needed to improve our understanding of the clinical impact of altered metabolites on brain development and outcome. IMPACT: NAA/Cho was reduced in the white matter, but not the gray matter of CHD neonates compared to healthy controls. No correlation to the 1-year neurodevelopmental outcome (Bayley-III) was found. While the rapid change of NAA/Cho with age might make it a sensitive marker for a delay in brain maturation, the relationship to neurodevelopmental outcome requires further investigation. Nature Publishing Group US 2022-08-22 2023 /pmc/articles/PMC10172141/ /pubmed/35995938 http://dx.doi.org/10.1038/s41390-022-02253-y 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 Clinical Research Article
Steger, Céline
Feldmann, Maria
Borns, Julia
Hagmann, Cornelia
Latal, Beatrice
Held, Ulrike
Jakab, András
O’Gorman Tuura, Ruth
Knirsch, Walter
Neurometabolic changes in neonates with congenital heart defects and their relation to neurodevelopmental outcome
title Neurometabolic changes in neonates with congenital heart defects and their relation to neurodevelopmental outcome
title_full Neurometabolic changes in neonates with congenital heart defects and their relation to neurodevelopmental outcome
title_fullStr Neurometabolic changes in neonates with congenital heart defects and their relation to neurodevelopmental outcome
title_full_unstemmed Neurometabolic changes in neonates with congenital heart defects and their relation to neurodevelopmental outcome
title_short Neurometabolic changes in neonates with congenital heart defects and their relation to neurodevelopmental outcome
title_sort neurometabolic changes in neonates with congenital heart defects and their relation to neurodevelopmental outcome
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172141/
https://www.ncbi.nlm.nih.gov/pubmed/35995938
http://dx.doi.org/10.1038/s41390-022-02253-y
work_keys_str_mv AT stegerceline neurometabolicchangesinneonateswithcongenitalheartdefectsandtheirrelationtoneurodevelopmentaloutcome
AT feldmannmaria neurometabolicchangesinneonateswithcongenitalheartdefectsandtheirrelationtoneurodevelopmentaloutcome
AT bornsjulia neurometabolicchangesinneonateswithcongenitalheartdefectsandtheirrelationtoneurodevelopmentaloutcome
AT hagmanncornelia neurometabolicchangesinneonateswithcongenitalheartdefectsandtheirrelationtoneurodevelopmentaloutcome
AT latalbeatrice neurometabolicchangesinneonateswithcongenitalheartdefectsandtheirrelationtoneurodevelopmentaloutcome
AT heldulrike neurometabolicchangesinneonateswithcongenitalheartdefectsandtheirrelationtoneurodevelopmentaloutcome
AT jakabandras neurometabolicchangesinneonateswithcongenitalheartdefectsandtheirrelationtoneurodevelopmentaloutcome
AT ogormantuuraruth neurometabolicchangesinneonateswithcongenitalheartdefectsandtheirrelationtoneurodevelopmentaloutcome
AT knirschwalter neurometabolicchangesinneonateswithcongenitalheartdefectsandtheirrelationtoneurodevelopmentaloutcome