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Arterial spin labeling characterization of cerebral perfusion during normal maturation from late childhood into adulthood: normal ‘reference range' values and their use in clinical studies
The human brain changes structurally and functionally during adolescence, with associated alterations in cerebral perfusion. We performed dynamic arterial spin labeling (ASL) magnetic resonance imaging in healthy subjects between 8 and 32 years of age, to investigate changes in cerebral hemodynamics...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013758/ https://www.ncbi.nlm.nih.gov/pubmed/24496173 http://dx.doi.org/10.1038/jcbfm.2014.17 |
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author | Hales, Patrick W Kawadler, Jamie M Aylett, Sarah E Kirkham, Fenella J Clark, Christopher A |
author_facet | Hales, Patrick W Kawadler, Jamie M Aylett, Sarah E Kirkham, Fenella J Clark, Christopher A |
author_sort | Hales, Patrick W |
collection | PubMed |
description | The human brain changes structurally and functionally during adolescence, with associated alterations in cerebral perfusion. We performed dynamic arterial spin labeling (ASL) magnetic resonance imaging in healthy subjects between 8 and 32 years of age, to investigate changes in cerebral hemodynamics during normal development. In addition, an inversion recovery sequence allowed quantification of changes in longitudinal relaxation time (T(1)) and equilibrium longitudinal magnetization (M(0)). We present mean and reference ranges for normal values of T(1), M(0), cerebral blood flow (CBF), bolus arrival time, and bolus duration in cortical gray matter, to provide a tool for identifying age-matched perfusion abnormalities in this age range in clinical studies. Cerebral blood flow and T(1) relaxation times were negatively correlated with age, without gender or hemisphere differences. The same was true for M(0) anteriorly, but posteriorly, males but not females showed a significant decline in M(0) with increasing age. Two examples of the clinical utility of these data in identifying age-matched perfusion abnormalities, in Sturge–Weber syndrome and sickle cell anemia, are illustrated. |
format | Online Article Text |
id | pubmed-4013758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40137582014-05-13 Arterial spin labeling characterization of cerebral perfusion during normal maturation from late childhood into adulthood: normal ‘reference range' values and their use in clinical studies Hales, Patrick W Kawadler, Jamie M Aylett, Sarah E Kirkham, Fenella J Clark, Christopher A J Cereb Blood Flow Metab Original Article The human brain changes structurally and functionally during adolescence, with associated alterations in cerebral perfusion. We performed dynamic arterial spin labeling (ASL) magnetic resonance imaging in healthy subjects between 8 and 32 years of age, to investigate changes in cerebral hemodynamics during normal development. In addition, an inversion recovery sequence allowed quantification of changes in longitudinal relaxation time (T(1)) and equilibrium longitudinal magnetization (M(0)). We present mean and reference ranges for normal values of T(1), M(0), cerebral blood flow (CBF), bolus arrival time, and bolus duration in cortical gray matter, to provide a tool for identifying age-matched perfusion abnormalities in this age range in clinical studies. Cerebral blood flow and T(1) relaxation times were negatively correlated with age, without gender or hemisphere differences. The same was true for M(0) anteriorly, but posteriorly, males but not females showed a significant decline in M(0) with increasing age. Two examples of the clinical utility of these data in identifying age-matched perfusion abnormalities, in Sturge–Weber syndrome and sickle cell anemia, are illustrated. Nature Publishing Group 2014-05 2014-02-05 /pmc/articles/PMC4013758/ /pubmed/24496173 http://dx.doi.org/10.1038/jcbfm.2014.17 Text en Copyright © 2014 International Society for Cerebral Blood Flow & Metabolism, Inc. http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Original Article Hales, Patrick W Kawadler, Jamie M Aylett, Sarah E Kirkham, Fenella J Clark, Christopher A Arterial spin labeling characterization of cerebral perfusion during normal maturation from late childhood into adulthood: normal ‘reference range' values and their use in clinical studies |
title | Arterial spin labeling characterization of cerebral perfusion during normal maturation from late childhood into adulthood: normal ‘reference range' values and their use in clinical studies |
title_full | Arterial spin labeling characterization of cerebral perfusion during normal maturation from late childhood into adulthood: normal ‘reference range' values and their use in clinical studies |
title_fullStr | Arterial spin labeling characterization of cerebral perfusion during normal maturation from late childhood into adulthood: normal ‘reference range' values and their use in clinical studies |
title_full_unstemmed | Arterial spin labeling characterization of cerebral perfusion during normal maturation from late childhood into adulthood: normal ‘reference range' values and their use in clinical studies |
title_short | Arterial spin labeling characterization of cerebral perfusion during normal maturation from late childhood into adulthood: normal ‘reference range' values and their use in clinical studies |
title_sort | arterial spin labeling characterization of cerebral perfusion during normal maturation from late childhood into adulthood: normal ‘reference range' values and their use in clinical studies |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013758/ https://www.ncbi.nlm.nih.gov/pubmed/24496173 http://dx.doi.org/10.1038/jcbfm.2014.17 |
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