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Quantitative T(1) and T(2) MRI signal characteristics in the human brain: different patterns of MR contrasts in normal ageing

OBJECTIVE: The objective of this study was to examine age-dependent changes in both T(1)-weighted and T(2)-weighted image contrasts and spin-echo T(2) relaxation time in the human brain during healthy ageing. METHODS: A total of 37 participants between the ages of 49 and 87 years old were scanned wi...

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Autores principales: Knight, Michael J., McCann, Bryony, Tsivos, Demitra, Couthard, Elizabeth, Kauppinen, Risto A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124042/
https://www.ncbi.nlm.nih.gov/pubmed/27333937
http://dx.doi.org/10.1007/s10334-016-0573-0
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author Knight, Michael J.
McCann, Bryony
Tsivos, Demitra
Couthard, Elizabeth
Kauppinen, Risto A.
author_facet Knight, Michael J.
McCann, Bryony
Tsivos, Demitra
Couthard, Elizabeth
Kauppinen, Risto A.
author_sort Knight, Michael J.
collection PubMed
description OBJECTIVE: The objective of this study was to examine age-dependent changes in both T(1)-weighted and T(2)-weighted image contrasts and spin-echo T(2) relaxation time in the human brain during healthy ageing. METHODS: A total of 37 participants between the ages of 49 and 87 years old were scanned with a 3 Tesla system, using T(1)-weighted, T(2) weighted and quantitative spin-echo T(2) imaging. Contrast between image intensities and T(2) values was calculated for various regions, including between individual hippocampal subfields. RESULTS: The T(1) contrast-to-noise (CNR) and gray:white signal intensity ratio (GWR) did not change in the hippocampus, but it declined in the cingulate cortex with age. In contrast, T(2) CNR and GWR declined in both brain regions. T(2) relaxation time was almost constant in gray matter and most (but not all) hippocampal subfields, but increased substantially in white matter, pointing to an age effect on water relaxation in white matter. CONCLUSIONS: Changes in T(1) and T(2) MR characteristics influence the appearance of brain images in later life and should be considered in image analyses of aged subjects. It is speculated that alterations at the cell biology level, with concomitant alterations to the local magnetic environment, reduce dephasing and subsequently prolong spin-echo T(2) through reduced diffusion effects in later life. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10334-016-0573-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-51240422016-12-09 Quantitative T(1) and T(2) MRI signal characteristics in the human brain: different patterns of MR contrasts in normal ageing Knight, Michael J. McCann, Bryony Tsivos, Demitra Couthard, Elizabeth Kauppinen, Risto A. MAGMA Research Article OBJECTIVE: The objective of this study was to examine age-dependent changes in both T(1)-weighted and T(2)-weighted image contrasts and spin-echo T(2) relaxation time in the human brain during healthy ageing. METHODS: A total of 37 participants between the ages of 49 and 87 years old were scanned with a 3 Tesla system, using T(1)-weighted, T(2) weighted and quantitative spin-echo T(2) imaging. Contrast between image intensities and T(2) values was calculated for various regions, including between individual hippocampal subfields. RESULTS: The T(1) contrast-to-noise (CNR) and gray:white signal intensity ratio (GWR) did not change in the hippocampus, but it declined in the cingulate cortex with age. In contrast, T(2) CNR and GWR declined in both brain regions. T(2) relaxation time was almost constant in gray matter and most (but not all) hippocampal subfields, but increased substantially in white matter, pointing to an age effect on water relaxation in white matter. CONCLUSIONS: Changes in T(1) and T(2) MR characteristics influence the appearance of brain images in later life and should be considered in image analyses of aged subjects. It is speculated that alterations at the cell biology level, with concomitant alterations to the local magnetic environment, reduce dephasing and subsequently prolong spin-echo T(2) through reduced diffusion effects in later life. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10334-016-0573-0) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-06-22 2016 /pmc/articles/PMC5124042/ /pubmed/27333937 http://dx.doi.org/10.1007/s10334-016-0573-0 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Research Article
Knight, Michael J.
McCann, Bryony
Tsivos, Demitra
Couthard, Elizabeth
Kauppinen, Risto A.
Quantitative T(1) and T(2) MRI signal characteristics in the human brain: different patterns of MR contrasts in normal ageing
title Quantitative T(1) and T(2) MRI signal characteristics in the human brain: different patterns of MR contrasts in normal ageing
title_full Quantitative T(1) and T(2) MRI signal characteristics in the human brain: different patterns of MR contrasts in normal ageing
title_fullStr Quantitative T(1) and T(2) MRI signal characteristics in the human brain: different patterns of MR contrasts in normal ageing
title_full_unstemmed Quantitative T(1) and T(2) MRI signal characteristics in the human brain: different patterns of MR contrasts in normal ageing
title_short Quantitative T(1) and T(2) MRI signal characteristics in the human brain: different patterns of MR contrasts in normal ageing
title_sort quantitative t(1) and t(2) mri signal characteristics in the human brain: different patterns of mr contrasts in normal ageing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124042/
https://www.ncbi.nlm.nih.gov/pubmed/27333937
http://dx.doi.org/10.1007/s10334-016-0573-0
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