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Increased Risk of Aging-Related Neurodegenerative Disease after Traumatic Brain Injury

Traumatic brain injury (TBI) survivors frequently suffer from chronically progressive complications, including significantly increased risk of developing aging-related neurodegenerative disease. As advances in neurocritical care increase the number of TBI survivors, the impact and awareness of this...

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Autores principales: Barker, Sarah, Paul, Bindu D., Pieper, Andrew A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135798/
https://www.ncbi.nlm.nih.gov/pubmed/37189772
http://dx.doi.org/10.3390/biomedicines11041154
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author Barker, Sarah
Paul, Bindu D.
Pieper, Andrew A.
author_facet Barker, Sarah
Paul, Bindu D.
Pieper, Andrew A.
author_sort Barker, Sarah
collection PubMed
description Traumatic brain injury (TBI) survivors frequently suffer from chronically progressive complications, including significantly increased risk of developing aging-related neurodegenerative disease. As advances in neurocritical care increase the number of TBI survivors, the impact and awareness of this problem are growing. The mechanisms by which TBI increases the risk of developing aging-related neurodegenerative disease, however, are not completely understood. As a result, there are no protective treatments for patients. Here, we review the current literature surrounding the epidemiology and potential mechanistic relationships between brain injury and aging-related neurodegenerative disease. In addition to increasing the risk for developing all forms of dementia, the most prominent aging-related neurodegenerative conditions that are accelerated by TBI are amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), Parkinson’s disease (PD), and Alzheimer’s disease (AD), with ALS and FTD being the least well-established. Mechanistic links between TBI and all forms of dementia that are reviewed include oxidative stress, dysregulated proteostasis, and neuroinflammation. Disease-specific mechanistic links with TBI that are reviewed include TAR DNA binding protein 43 and motor cortex lesions in ALS and FTD; alpha-synuclein, dopaminergic cell death, and synergistic toxin exposure in PD; and brain insulin resistance, amyloid beta pathology, and tau pathology in AD. While compelling mechanistic links have been identified, significantly expanded investigation in the field is needed to develop therapies to protect TBI survivors from the increased risk of aging-related neurodegenerative disease.
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spelling pubmed-101357982023-04-28 Increased Risk of Aging-Related Neurodegenerative Disease after Traumatic Brain Injury Barker, Sarah Paul, Bindu D. Pieper, Andrew A. Biomedicines Review Traumatic brain injury (TBI) survivors frequently suffer from chronically progressive complications, including significantly increased risk of developing aging-related neurodegenerative disease. As advances in neurocritical care increase the number of TBI survivors, the impact and awareness of this problem are growing. The mechanisms by which TBI increases the risk of developing aging-related neurodegenerative disease, however, are not completely understood. As a result, there are no protective treatments for patients. Here, we review the current literature surrounding the epidemiology and potential mechanistic relationships between brain injury and aging-related neurodegenerative disease. In addition to increasing the risk for developing all forms of dementia, the most prominent aging-related neurodegenerative conditions that are accelerated by TBI are amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), Parkinson’s disease (PD), and Alzheimer’s disease (AD), with ALS and FTD being the least well-established. Mechanistic links between TBI and all forms of dementia that are reviewed include oxidative stress, dysregulated proteostasis, and neuroinflammation. Disease-specific mechanistic links with TBI that are reviewed include TAR DNA binding protein 43 and motor cortex lesions in ALS and FTD; alpha-synuclein, dopaminergic cell death, and synergistic toxin exposure in PD; and brain insulin resistance, amyloid beta pathology, and tau pathology in AD. While compelling mechanistic links have been identified, significantly expanded investigation in the field is needed to develop therapies to protect TBI survivors from the increased risk of aging-related neurodegenerative disease. MDPI 2023-04-11 /pmc/articles/PMC10135798/ /pubmed/37189772 http://dx.doi.org/10.3390/biomedicines11041154 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Barker, Sarah
Paul, Bindu D.
Pieper, Andrew A.
Increased Risk of Aging-Related Neurodegenerative Disease after Traumatic Brain Injury
title Increased Risk of Aging-Related Neurodegenerative Disease after Traumatic Brain Injury
title_full Increased Risk of Aging-Related Neurodegenerative Disease after Traumatic Brain Injury
title_fullStr Increased Risk of Aging-Related Neurodegenerative Disease after Traumatic Brain Injury
title_full_unstemmed Increased Risk of Aging-Related Neurodegenerative Disease after Traumatic Brain Injury
title_short Increased Risk of Aging-Related Neurodegenerative Disease after Traumatic Brain Injury
title_sort increased risk of aging-related neurodegenerative disease after traumatic brain injury
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135798/
https://www.ncbi.nlm.nih.gov/pubmed/37189772
http://dx.doi.org/10.3390/biomedicines11041154
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