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The Effect of Mild Traumatic Brain Injury on Cerebral Microbleeds in Aging

A traumatic brain injury (TBI) induces the formation of cerebral microbleeds (CMBs), which are associated with cognitive impairments, psychiatric disorders, and gait dysfunctions in patients. Elderly people frequently suffer TBIs, especially mild brain trauma (mTBI). Interestingly, aging is also an...

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Autores principales: Toth, Luca, Czigler, Andras, Horvath, Peter, Szarka, Nikolett, Kornyei, Balint, Toth, Arnold, Schwarcz, Attila, Ungvari, Zoltan, Buki, Andras, Toth, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514735/
https://www.ncbi.nlm.nih.gov/pubmed/34658836
http://dx.doi.org/10.3389/fnagi.2021.717391
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author Toth, Luca
Czigler, Andras
Horvath, Peter
Szarka, Nikolett
Kornyei, Balint
Toth, Arnold
Schwarcz, Attila
Ungvari, Zoltan
Buki, Andras
Toth, Peter
author_facet Toth, Luca
Czigler, Andras
Horvath, Peter
Szarka, Nikolett
Kornyei, Balint
Toth, Arnold
Schwarcz, Attila
Ungvari, Zoltan
Buki, Andras
Toth, Peter
author_sort Toth, Luca
collection PubMed
description A traumatic brain injury (TBI) induces the formation of cerebral microbleeds (CMBs), which are associated with cognitive impairments, psychiatric disorders, and gait dysfunctions in patients. Elderly people frequently suffer TBIs, especially mild brain trauma (mTBI). Interestingly, aging is also an independent risk factor for the development of CMBs. However, how TBI and aging may interact to promote the development of CMBs is not well established. In order to test the hypothesis that an mTBI exacerbates the development of CMBs in the elderly, we compared the number and cerebral distribution of CMBs and assessed them by analysing susceptibility weighted (SW) MRI in young (25 ± 10 years old, n = 18) and elder (72 ± 7 years old, n = 17) patients after an mTBI and in age-matched healthy subjects (young: 25 ± 6 years old, n = 20; aged: 68 ± 5 years old, n = 23). We found significantly more CMBs in elder patients after an mTBI compared with young patients; however, we did not observe a significant difference in the number of cerebral microhemorrhages between aged and aged patients with mTBI. The majority of CMBs were found supratentorially (lobar and basal ganglion). The lobar distribution of supratentorial CMBs showed that aging enhances the formation of parietal and occipital CMBs after mTBIs. This suggests that aging and mTBIs do not synergize in the induction of the development of CMBs, and that the different distribution of mTBI-induced CMBs in aged patients may lead to specific age-related clinical characteristics of mTBIs.
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spelling pubmed-85147352021-10-15 The Effect of Mild Traumatic Brain Injury on Cerebral Microbleeds in Aging Toth, Luca Czigler, Andras Horvath, Peter Szarka, Nikolett Kornyei, Balint Toth, Arnold Schwarcz, Attila Ungvari, Zoltan Buki, Andras Toth, Peter Front Aging Neurosci Neuroscience A traumatic brain injury (TBI) induces the formation of cerebral microbleeds (CMBs), which are associated with cognitive impairments, psychiatric disorders, and gait dysfunctions in patients. Elderly people frequently suffer TBIs, especially mild brain trauma (mTBI). Interestingly, aging is also an independent risk factor for the development of CMBs. However, how TBI and aging may interact to promote the development of CMBs is not well established. In order to test the hypothesis that an mTBI exacerbates the development of CMBs in the elderly, we compared the number and cerebral distribution of CMBs and assessed them by analysing susceptibility weighted (SW) MRI in young (25 ± 10 years old, n = 18) and elder (72 ± 7 years old, n = 17) patients after an mTBI and in age-matched healthy subjects (young: 25 ± 6 years old, n = 20; aged: 68 ± 5 years old, n = 23). We found significantly more CMBs in elder patients after an mTBI compared with young patients; however, we did not observe a significant difference in the number of cerebral microhemorrhages between aged and aged patients with mTBI. The majority of CMBs were found supratentorially (lobar and basal ganglion). The lobar distribution of supratentorial CMBs showed that aging enhances the formation of parietal and occipital CMBs after mTBIs. This suggests that aging and mTBIs do not synergize in the induction of the development of CMBs, and that the different distribution of mTBI-induced CMBs in aged patients may lead to specific age-related clinical characteristics of mTBIs. Frontiers Media S.A. 2021-09-30 /pmc/articles/PMC8514735/ /pubmed/34658836 http://dx.doi.org/10.3389/fnagi.2021.717391 Text en Copyright © 2021 Toth, Czigler, Horvath, Szarka, Kornyei, Toth, Schwarcz, Ungvari, Buki and Toth. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Toth, Luca
Czigler, Andras
Horvath, Peter
Szarka, Nikolett
Kornyei, Balint
Toth, Arnold
Schwarcz, Attila
Ungvari, Zoltan
Buki, Andras
Toth, Peter
The Effect of Mild Traumatic Brain Injury on Cerebral Microbleeds in Aging
title The Effect of Mild Traumatic Brain Injury on Cerebral Microbleeds in Aging
title_full The Effect of Mild Traumatic Brain Injury on Cerebral Microbleeds in Aging
title_fullStr The Effect of Mild Traumatic Brain Injury on Cerebral Microbleeds in Aging
title_full_unstemmed The Effect of Mild Traumatic Brain Injury on Cerebral Microbleeds in Aging
title_short The Effect of Mild Traumatic Brain Injury on Cerebral Microbleeds in Aging
title_sort effect of mild traumatic brain injury on cerebral microbleeds in aging
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514735/
https://www.ncbi.nlm.nih.gov/pubmed/34658836
http://dx.doi.org/10.3389/fnagi.2021.717391
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