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Widespread age-related differences in the human brain microstructure revealed by quantitative magnetic resonance imaging()
A pressing need exists to disentangle age-related changes from pathologic neurodegeneration. This study aims to characterize the spatial pattern and age-related differences of biologically relevant measures in vivo over the course of normal aging. Quantitative multiparameter maps that provide neuroi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4024196/ https://www.ncbi.nlm.nih.gov/pubmed/24656835 http://dx.doi.org/10.1016/j.neurobiolaging.2014.02.008 |
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author | Callaghan, Martina F. Freund, Patrick Draganski, Bogdan Anderson, Elaine Cappelletti, Marinella Chowdhury, Rumana Diedrichsen, Joern FitzGerald, Thomas H.B. Smittenaar, Peter Helms, Gunther Lutti, Antoine Weiskopf, Nikolaus |
author_facet | Callaghan, Martina F. Freund, Patrick Draganski, Bogdan Anderson, Elaine Cappelletti, Marinella Chowdhury, Rumana Diedrichsen, Joern FitzGerald, Thomas H.B. Smittenaar, Peter Helms, Gunther Lutti, Antoine Weiskopf, Nikolaus |
author_sort | Callaghan, Martina F. |
collection | PubMed |
description | A pressing need exists to disentangle age-related changes from pathologic neurodegeneration. This study aims to characterize the spatial pattern and age-related differences of biologically relevant measures in vivo over the course of normal aging. Quantitative multiparameter maps that provide neuroimaging biomarkers for myelination and iron levels, parameters sensitive to aging, were acquired from 138 healthy volunteers (age range: 19–75 years). Whole-brain voxel-wise analysis revealed a global pattern of age-related degeneration. Significant demyelination occurred principally in the white matter. The observed age-related differences in myelination were anatomically specific. In line with invasive histologic reports, higher age-related differences were seen in the genu of the corpus callosum than the splenium. Iron levels were significantly increased in the basal ganglia, red nucleus, and extensive cortical regions but decreased along the superior occipitofrontal fascicle and optic radiation. This whole-brain pattern of age-associated microstructural differences in the asymptomatic population provides insight into the neurobiology of aging. The results help build a quantitative baseline from which to examine and draw a dividing line between healthy aging and pathologic neurodegeneration. |
format | Online Article Text |
id | pubmed-4024196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-40241962014-08-01 Widespread age-related differences in the human brain microstructure revealed by quantitative magnetic resonance imaging() Callaghan, Martina F. Freund, Patrick Draganski, Bogdan Anderson, Elaine Cappelletti, Marinella Chowdhury, Rumana Diedrichsen, Joern FitzGerald, Thomas H.B. Smittenaar, Peter Helms, Gunther Lutti, Antoine Weiskopf, Nikolaus Neurobiol Aging Regular Article A pressing need exists to disentangle age-related changes from pathologic neurodegeneration. This study aims to characterize the spatial pattern and age-related differences of biologically relevant measures in vivo over the course of normal aging. Quantitative multiparameter maps that provide neuroimaging biomarkers for myelination and iron levels, parameters sensitive to aging, were acquired from 138 healthy volunteers (age range: 19–75 years). Whole-brain voxel-wise analysis revealed a global pattern of age-related degeneration. Significant demyelination occurred principally in the white matter. The observed age-related differences in myelination were anatomically specific. In line with invasive histologic reports, higher age-related differences were seen in the genu of the corpus callosum than the splenium. Iron levels were significantly increased in the basal ganglia, red nucleus, and extensive cortical regions but decreased along the superior occipitofrontal fascicle and optic radiation. This whole-brain pattern of age-associated microstructural differences in the asymptomatic population provides insight into the neurobiology of aging. The results help build a quantitative baseline from which to examine and draw a dividing line between healthy aging and pathologic neurodegeneration. Elsevier 2014-08 /pmc/articles/PMC4024196/ /pubmed/24656835 http://dx.doi.org/10.1016/j.neurobiolaging.2014.02.008 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Regular Article Callaghan, Martina F. Freund, Patrick Draganski, Bogdan Anderson, Elaine Cappelletti, Marinella Chowdhury, Rumana Diedrichsen, Joern FitzGerald, Thomas H.B. Smittenaar, Peter Helms, Gunther Lutti, Antoine Weiskopf, Nikolaus Widespread age-related differences in the human brain microstructure revealed by quantitative magnetic resonance imaging() |
title | Widespread age-related differences in the human brain microstructure revealed by quantitative magnetic resonance imaging() |
title_full | Widespread age-related differences in the human brain microstructure revealed by quantitative magnetic resonance imaging() |
title_fullStr | Widespread age-related differences in the human brain microstructure revealed by quantitative magnetic resonance imaging() |
title_full_unstemmed | Widespread age-related differences in the human brain microstructure revealed by quantitative magnetic resonance imaging() |
title_short | Widespread age-related differences in the human brain microstructure revealed by quantitative magnetic resonance imaging() |
title_sort | widespread age-related differences in the human brain microstructure revealed by quantitative magnetic resonance imaging() |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4024196/ https://www.ncbi.nlm.nih.gov/pubmed/24656835 http://dx.doi.org/10.1016/j.neurobiolaging.2014.02.008 |
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