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Quantitative T1 mapping of the normal brain from early infancy to adulthood

BACKGROUND: Quantitative mapping of MRI relaxation times is expected to uncover pathological processes in the brain more subtly than standard MRI techniques with weighted contrasts. So far, however, most mapping techniques suffer from a long measuring time, low spatial resolution or even sensitivity...

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Autores principales: Gräfe, Daniel, Frahm, Jens, Merkenschlager, Andreas, Voit, Dirk, Hirsch, Franz Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7897197/
https://www.ncbi.nlm.nih.gov/pubmed/33068131
http://dx.doi.org/10.1007/s00247-020-04842-7
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author Gräfe, Daniel
Frahm, Jens
Merkenschlager, Andreas
Voit, Dirk
Hirsch, Franz Wolfgang
author_facet Gräfe, Daniel
Frahm, Jens
Merkenschlager, Andreas
Voit, Dirk
Hirsch, Franz Wolfgang
author_sort Gräfe, Daniel
collection PubMed
description BACKGROUND: Quantitative mapping of MRI relaxation times is expected to uncover pathological processes in the brain more subtly than standard MRI techniques with weighted contrasts. So far, however, most mapping techniques suffer from a long measuring time, low spatial resolution or even sensitivity to magnetic field inhomogeneity. OBJECTIVE: To obtain T1 relaxation times of the normal brain from early infancy to adulthood using a novel technique for fast and accurate T1 mapping at high spatial resolution. MATERIALS AND METHODS: We performed whole-brain T1 mapping within less than 3 min in 100 patients between 2 months and 18 years of age with normal brain at a field strength of 3 T. We analyzed T1 relaxation times in several gray-matter nuclei and white matter. Subsequently, we derived regression equations for mean value and confidence interval. RESULTS: T1 relaxation times of the pediatric brain rapidly decrease in all regions within the first 3 years of age, followed by a significantly weaker decrease until adulthood. These characteristics are more pronounced in white matter than in deep gray matter. CONCLUSION: Regardless of age, quantitative T1 mapping of the pediatric brain is feasible in clinical practice. Normal age-dependent values should contribute to improved discrimination of subtle intracerebral alterations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00247-020-04842-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-78971972021-03-05 Quantitative T1 mapping of the normal brain from early infancy to adulthood Gräfe, Daniel Frahm, Jens Merkenschlager, Andreas Voit, Dirk Hirsch, Franz Wolfgang Pediatr Radiol Original Article BACKGROUND: Quantitative mapping of MRI relaxation times is expected to uncover pathological processes in the brain more subtly than standard MRI techniques with weighted contrasts. So far, however, most mapping techniques suffer from a long measuring time, low spatial resolution or even sensitivity to magnetic field inhomogeneity. OBJECTIVE: To obtain T1 relaxation times of the normal brain from early infancy to adulthood using a novel technique for fast and accurate T1 mapping at high spatial resolution. MATERIALS AND METHODS: We performed whole-brain T1 mapping within less than 3 min in 100 patients between 2 months and 18 years of age with normal brain at a field strength of 3 T. We analyzed T1 relaxation times in several gray-matter nuclei and white matter. Subsequently, we derived regression equations for mean value and confidence interval. RESULTS: T1 relaxation times of the pediatric brain rapidly decrease in all regions within the first 3 years of age, followed by a significantly weaker decrease until adulthood. These characteristics are more pronounced in white matter than in deep gray matter. CONCLUSION: Regardless of age, quantitative T1 mapping of the pediatric brain is feasible in clinical practice. Normal age-dependent values should contribute to improved discrimination of subtle intracerebral alterations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00247-020-04842-7) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-10-17 2021 /pmc/articles/PMC7897197/ /pubmed/33068131 http://dx.doi.org/10.1007/s00247-020-04842-7 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Gräfe, Daniel
Frahm, Jens
Merkenschlager, Andreas
Voit, Dirk
Hirsch, Franz Wolfgang
Quantitative T1 mapping of the normal brain from early infancy to adulthood
title Quantitative T1 mapping of the normal brain from early infancy to adulthood
title_full Quantitative T1 mapping of the normal brain from early infancy to adulthood
title_fullStr Quantitative T1 mapping of the normal brain from early infancy to adulthood
title_full_unstemmed Quantitative T1 mapping of the normal brain from early infancy to adulthood
title_short Quantitative T1 mapping of the normal brain from early infancy to adulthood
title_sort quantitative t1 mapping of the normal brain from early infancy to adulthood
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7897197/
https://www.ncbi.nlm.nih.gov/pubmed/33068131
http://dx.doi.org/10.1007/s00247-020-04842-7
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