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

Author:

Barker Sarah12345,Paul Bindu D.6789ORCID,Pieper Andrew A.123451011

Affiliation:

1. Center for Brain Health Medicines, Harrington Discovery Institute, University Hospitals Cleveland Medical Center, Cleveland, OH 44106, USA

2. Department of Psychiatry, Case Western Reserve University, Cleveland, OH 44106, USA

3. Geriatric Psychiatry, GRECC, Louis Stokes Cleveland VA Medical Center, Cleveland, OH 44106, USA

4. Institute for Transformative Molecular Medicine, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA

5. Department of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA

6. Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21211, USA

7. Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21211, USA

8. The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21211, USA

9. Lieber Institute for Brain Development, Baltimore, MD 21205, USA

10. Department of Neuroscience, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA

11. Translational Therapeutics Core, Cleveland Alzheimer’s Disease Research Center, Cleveland, OH 44106, USA

Abstract

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.

Funder

Case Western Reserve University

Brockman Foundation, Department of Veterans Affairs Merit Award

Elizabeth Ring Mather & William Gwinn Mather Fund

S. Livingston Samuel Mather Trust

G.R. Lincoln Family Foundation

Wick Foundation

Leonard Krieger Fund of the Cleveland Foundation

Maxine and Lester Stoller Parkinson’s Research Fund

Gordon & Evie Safran

Louis Stokes VA Medical Center resources and facilities

Translational Therapeutics Core of the Cleveland Alzheimer’s Disease Research Center

American Heart Association

Paul Allen Foundation Initiative in Brain Health and Cognitive Impairment

NIH NIDA

Catalyst Award from Johns Hopkins University

The Alzheimer’s Disease Translational Data Science Training Program

Case Western Medical Scientist Training program

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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