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An In Vivo Study on Brain Microstructure in Biological and Chronological Ageing

This study aimed to investigate whether magnetization transfer imaging (MTI) parameters of cortical gray and white matter and subcortical gray matter structures differ between subjects enriched for human familial longevity and control subjects to provide a thorough description of the brain phenotype...

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Autores principales: Altmann-Schneider, Irmhild, de Craen, Anton J. M., van den Berg-Huysmans, Annette A., Slagboom, Pieternella, Westendorp, Rudi G.J., van Buchem, Mark A., van der Grond, Jeroen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373824/
https://www.ncbi.nlm.nih.gov/pubmed/25807271
http://dx.doi.org/10.1371/journal.pone.0120778
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author Altmann-Schneider, Irmhild
de Craen, Anton J. M.
van den Berg-Huysmans, Annette A.
Slagboom, Pieternella
Westendorp, Rudi G.J.
van Buchem, Mark A.
van der Grond, Jeroen
author_facet Altmann-Schneider, Irmhild
de Craen, Anton J. M.
van den Berg-Huysmans, Annette A.
Slagboom, Pieternella
Westendorp, Rudi G.J.
van Buchem, Mark A.
van der Grond, Jeroen
author_sort Altmann-Schneider, Irmhild
collection PubMed
description This study aimed to investigate whether magnetization transfer imaging (MTI) parameters of cortical gray and white matter and subcortical gray matter structures differ between subjects enriched for human familial longevity and control subjects to provide a thorough description of the brain phenotype of familial longevity. Moreover, we aimed to describe cerebral ageing effects on MTI parameters in an elderly cohort. All subjects were included from the Leiden Longevity Study and underwent 3 Tesla MTI of the brain. In total, 183 offspring of nonagenarian siblings, who are enriched for familial factors of longevity, were contrasted with 163 environmentally and age-matched controls. No differences in cortical and subcortical gray matter and white matter MTI parameters were found between offspring and control subjects using histogram-based and voxel-wise analyses. Cortical gray matter and white matter MTI parameters decreased with increasing chronological age (all p < 0.001). Decrease of white matter magnetization transfer ratio (MTR) was homogeneous throughout the whole mean white matter skeleton except for parts of the callosal splenium and partly the posterior limb of the internal capsule and superior region of the corona radiata (p < 0.05). Mean MTR of subcortical gray matter structures decreased with increasing age (p amygdala, caudate nucleus and putamen < 0.001; p pallidum = 0.001, p thalamus = 0.002). In conclusion, the brain phenotype of human familial longevity is - at a mean age of 66 years - not characterized by preserved macromolecular brain tissue integrity.
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spelling pubmed-43738242015-03-27 An In Vivo Study on Brain Microstructure in Biological and Chronological Ageing Altmann-Schneider, Irmhild de Craen, Anton J. M. van den Berg-Huysmans, Annette A. Slagboom, Pieternella Westendorp, Rudi G.J. van Buchem, Mark A. van der Grond, Jeroen PLoS One Research Article This study aimed to investigate whether magnetization transfer imaging (MTI) parameters of cortical gray and white matter and subcortical gray matter structures differ between subjects enriched for human familial longevity and control subjects to provide a thorough description of the brain phenotype of familial longevity. Moreover, we aimed to describe cerebral ageing effects on MTI parameters in an elderly cohort. All subjects were included from the Leiden Longevity Study and underwent 3 Tesla MTI of the brain. In total, 183 offspring of nonagenarian siblings, who are enriched for familial factors of longevity, were contrasted with 163 environmentally and age-matched controls. No differences in cortical and subcortical gray matter and white matter MTI parameters were found between offspring and control subjects using histogram-based and voxel-wise analyses. Cortical gray matter and white matter MTI parameters decreased with increasing chronological age (all p < 0.001). Decrease of white matter magnetization transfer ratio (MTR) was homogeneous throughout the whole mean white matter skeleton except for parts of the callosal splenium and partly the posterior limb of the internal capsule and superior region of the corona radiata (p < 0.05). Mean MTR of subcortical gray matter structures decreased with increasing age (p amygdala, caudate nucleus and putamen < 0.001; p pallidum = 0.001, p thalamus = 0.002). In conclusion, the brain phenotype of human familial longevity is - at a mean age of 66 years - not characterized by preserved macromolecular brain tissue integrity. Public Library of Science 2015-03-25 /pmc/articles/PMC4373824/ /pubmed/25807271 http://dx.doi.org/10.1371/journal.pone.0120778 Text en © 2015 Altmann-Schneider et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Altmann-Schneider, Irmhild
de Craen, Anton J. M.
van den Berg-Huysmans, Annette A.
Slagboom, Pieternella
Westendorp, Rudi G.J.
van Buchem, Mark A.
van der Grond, Jeroen
An In Vivo Study on Brain Microstructure in Biological and Chronological Ageing
title An In Vivo Study on Brain Microstructure in Biological and Chronological Ageing
title_full An In Vivo Study on Brain Microstructure in Biological and Chronological Ageing
title_fullStr An In Vivo Study on Brain Microstructure in Biological and Chronological Ageing
title_full_unstemmed An In Vivo Study on Brain Microstructure in Biological and Chronological Ageing
title_short An In Vivo Study on Brain Microstructure in Biological and Chronological Ageing
title_sort in vivo study on brain microstructure in biological and chronological ageing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373824/
https://www.ncbi.nlm.nih.gov/pubmed/25807271
http://dx.doi.org/10.1371/journal.pone.0120778
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