| Literature DB >> 30299493 |
Gabriel S Walt1, Hannah M Burris1, Christopher B Brady1,2,3, Keith R Spencer1, Victor E Alvarez1,2,4,5, Bertrand R Huber1,6,2,4,5, Latease Guilderson1, Nazifa Abdul Rauf1, Derek Collins1, Tarnjit Singh1, Rebecca Mathias1,2, James G Averill7, Sean E Walker7, Ian Robey7, Ann C McKee1,2,4,5,8, Neil W Kowall1,2,4, Thor D Stein1,4,5,8.
Abstract
Chronic traumatic encephalopathy (CTE) is a progressive neurodegenerative disorder linked to repetitive head impacts and has been associated with amyotrophic lateral sclerosis (ALS), a fatal, degenerative neuromuscular disorder. The Department of Veterans Affairs Biorepository Brain Bank (VABBB) is a tissue repository that collects antemortem disease progression data and postmortem central nervous system tissue from veterans with ALS. We set out to determine the frequency of co-morbid ALS and CTE in the VABBB cohort and to characterize the clinical, genetic, and pathological distinctions between participants with ALS only and those with both ALS and CTE (ALS+CTE). Of 155 participants, 9 (5.8%) had neuropathologically confirmed ALS+CTE. Participants with ALS+CTE were more likely to have a history of traumatic brain injury (p < 0.001), served during the first Persian Gulf War (p < 0.05), and to have more severe tau pathology within the frontal cortex and spinal cord (p < 0.05). The most common exposures to head impacts included contact sports (n = 5) and military service (n = 2). Clinically, participants with ALS+CTE were more likely to have bulbar onset ALS (p = 0.006), behavioral changes (p = 0.002), and/or mood changes (p < 0.001). Overall, compared with ALS in isolation, comorbid ALS+CTE is associated with a history of TBI and has a distinct clinical and pathological presentation.Entities:
Mesh:
Year: 2018 PMID: 30299493 PMCID: PMC6927868 DOI: 10.1093/jnen/nly092
Source DB: PubMed Journal: J Neuropathol Exp Neurol ISSN: 0022-3069 Impact factor: 3.685