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Maturation and degeneration of the human brainstem across the adult lifespan

Brainstem tissue microstructural properties change across the adult lifespan. However, studies elucidating the biological processes that govern brainstem maturation and degeneration in-vivo are lacking. In the present work, conducted on a large cohort of 140 cognitively unimpaired subjects spanning...

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Autores principales: Bouhrara, Mustapha, Cortina, Luis E., Khattar, Nikkita, Rejimon, Abinand C., Ajamu, Samuel, Cezayirli, Defne S., Spencer, Richard G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8221341/
https://www.ncbi.nlm.nih.gov/pubmed/34115614
http://dx.doi.org/10.18632/aging.203183
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author Bouhrara, Mustapha
Cortina, Luis E.
Khattar, Nikkita
Rejimon, Abinand C.
Ajamu, Samuel
Cezayirli, Defne S.
Spencer, Richard G.
author_facet Bouhrara, Mustapha
Cortina, Luis E.
Khattar, Nikkita
Rejimon, Abinand C.
Ajamu, Samuel
Cezayirli, Defne S.
Spencer, Richard G.
author_sort Bouhrara, Mustapha
collection PubMed
description Brainstem tissue microstructural properties change across the adult lifespan. However, studies elucidating the biological processes that govern brainstem maturation and degeneration in-vivo are lacking. In the present work, conducted on a large cohort of 140 cognitively unimpaired subjects spanning a wide age range of 21 to 94 years, we implemented a multi-parameter approach to characterize the sex- and age differences. In addition, we examined regional correlations between myelin water fraction (MWF), a direct measure of myelin content, and diffusion tensor imaging indices, and transverse and longitudinal relaxation rates to evaluate whether these metrics provide information complementary to MWF. We observed region-dependent differences in myelin content and axonal density with age and found that both exhibit an inverted U-shape association with age in several brainstem substructures. We emphasize that the microstructural differences captured by our distinct MRI metrics, along with their weak associations with MWF, strongly indicate the potential of using these outcome measures in a multi-parametric approach. Furthermore, our results support the gain-predicts-loss hypothesis of tissue maturation and degeneration in the brainstem. Indeed, our results indicate that myelination follows a temporally symmetric time course across the adult life span, while axons appear to degenerate significantly more rapidly than they mature.
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spelling pubmed-82213412021-06-26 Maturation and degeneration of the human brainstem across the adult lifespan Bouhrara, Mustapha Cortina, Luis E. Khattar, Nikkita Rejimon, Abinand C. Ajamu, Samuel Cezayirli, Defne S. Spencer, Richard G. Aging (Albany NY) Research Paper Brainstem tissue microstructural properties change across the adult lifespan. However, studies elucidating the biological processes that govern brainstem maturation and degeneration in-vivo are lacking. In the present work, conducted on a large cohort of 140 cognitively unimpaired subjects spanning a wide age range of 21 to 94 years, we implemented a multi-parameter approach to characterize the sex- and age differences. In addition, we examined regional correlations between myelin water fraction (MWF), a direct measure of myelin content, and diffusion tensor imaging indices, and transverse and longitudinal relaxation rates to evaluate whether these metrics provide information complementary to MWF. We observed region-dependent differences in myelin content and axonal density with age and found that both exhibit an inverted U-shape association with age in several brainstem substructures. We emphasize that the microstructural differences captured by our distinct MRI metrics, along with their weak associations with MWF, strongly indicate the potential of using these outcome measures in a multi-parametric approach. Furthermore, our results support the gain-predicts-loss hypothesis of tissue maturation and degeneration in the brainstem. Indeed, our results indicate that myelination follows a temporally symmetric time course across the adult life span, while axons appear to degenerate significantly more rapidly than they mature. Impact Journals 2021-06-11 /pmc/articles/PMC8221341/ /pubmed/34115614 http://dx.doi.org/10.18632/aging.203183 Text en Copyright: © 2021 Bouhrara et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Bouhrara, Mustapha
Cortina, Luis E.
Khattar, Nikkita
Rejimon, Abinand C.
Ajamu, Samuel
Cezayirli, Defne S.
Spencer, Richard G.
Maturation and degeneration of the human brainstem across the adult lifespan
title Maturation and degeneration of the human brainstem across the adult lifespan
title_full Maturation and degeneration of the human brainstem across the adult lifespan
title_fullStr Maturation and degeneration of the human brainstem across the adult lifespan
title_full_unstemmed Maturation and degeneration of the human brainstem across the adult lifespan
title_short Maturation and degeneration of the human brainstem across the adult lifespan
title_sort maturation and degeneration of the human brainstem across the adult lifespan
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8221341/
https://www.ncbi.nlm.nih.gov/pubmed/34115614
http://dx.doi.org/10.18632/aging.203183
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