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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
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.
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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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