Abstract
BackgroundThe initiation, anatomic pattern, and extent of tau spread in traumatic brain injury (TBI), and the mechanism by which TBI leads to long-term tau pathology, remain controversial. Some studies suggest that moderate to severe TBI is sufficient to promote tau pathology; however, others suggest that it is simply a consequence of aging. We therefore conducted a systematic narrative review of the literature addressing whether a single moderate to severe head injury leads to long-term development of tauopathy in both humans and animal models.MethodsStudies considered for inclusion in this review assessed a single moderate to severe TBI, assessed tau pathology at long-term timepoints post-injury, comprised experimental or observational studies, and were peer-reviewed and published in English. Databases searched included: PUBMED, NCBI-PMC, EMBASE, Web of Science, Academic Search Premiere, and APA Psychnet. Search results were uploaded to Covidence®, duplicates were removed, and articles underwent an abstract and full-text screening process. Data were then extracted and articles assessed for risk of bias.FindingsOf 4,150 studies screened, 26 were eligible for inclusion, of which 17 were human studies, 8 were preclinical animal studies, and 1 included both human and preclinical animal studies. Most studies had low to moderate risk of bias. Most human and animal studies (n = 12 and 9, respectively) suggested that a single moderate to severe TBI resulted in greater development of long-term tauopathy compared to no history of head injury. This conclusion should be interpreted with caution, however, due to several limitations: small sample sizes; inconsistencies in controlling for confounding factors that may have affected tau pathology (e.g., family history of dementia or neurological illnesses, apolipoprotein E genotype, etc.), inclusion of mostly males, and variation in reporting injury parameters.InterpretationResults indicate that a single moderate to severe TBI leads to greater chronic development of tauopathy compared to no history of head injury. This implies that tau pathology induced may not be transient, but can progressively develop over time in both humans and animal models. Targeting these tau changes for therapeutic intervention should be further explored to elucidate if disease progression can be reversed or mitigated.
Highlights
Traumatic brain injury (TBI) is defined as a physical impact to the head that disrupts the physiological function of the brain [16, 31]
The individual human studies assessed in this review had the following study characteristics: type of study design, injury severity, how the injury was rated, injury type, sample size and number of males and females, age at time of assessment, inclusion and exclusion criteria for samples or the sample population recruited, post-traumatic brain injury (TBI) interval, type of tau assessment, the findings of the individual studies, and if those findings supported the conclusion of long-term development of tau pathology
Results of individual studies There were a total of 18 reports that included human assessment of tau pathology chronically post Moderate to severe TBI (msTBI), while only 9 articles assessed this in preclinical animal models
Summary
Traumatic brain injury (TBI) is defined as a physical impact to the head that disrupts the physiological function of the brain [16, 31]. Around 69 million people worldwide experience a TBI, and in the United States, approximately 5.3 million individuals are living with a TBI-related disability [16, 65, 87]. This places a significant emotional and economic toll on society and a compelling need to understand the sequelae that occur after a brain injury, since no treatments or cures exist [64]. We conducted a systematic narrative review of the literature addressing whether a single moderate to severe head injury leads to long-term development of tauopathy in both humans and animal models
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