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Inflammatory biomarkers for neurobehavioral dysregulation in former American football players: findings from the DIAGNOSE CTE Research Project
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Author
van Amerongen, S.Pulukuri, S.V.
Tuz-Zahra, F.
Tripodis, Y.
Cherry, J.D.
Bernick, C.
Geda, Y.E.
Wethe, J.V.
Katz, D.I.
Alosco, M.L.
Adler, C.H.
Balcer, L.J.
Ashton, N.J.
Blennow, K.
Zetterberg, H.
Daneshvar, D.H.
Colasurdo, E.A.
Iliff, J.J.
Li, G.
Peskind, E.R.
Shenton, M.E.
Reiman, E.M.
Cummings, J.L.
Stern, R.A.
Affiliation
Banner Alzheimer’s Institute, University of ArizonaIssue Date
2024-02-09Keywords
BiomarkersChronic traumatic encephalopathy
CSF
IL-6
Neurodegeneration
Neurofilament light chain protein
Neuroinflammation
Neuropsychiatric symptoms
Repetitive head impacts
Traumatic encephalopathy syndrome
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BioMed Central LtdCitation
van Amerongen, S., Pulukuri, S.V., Tuz-Zahra, F. et al. Inflammatory biomarkers for neurobehavioral dysregulation in former American football players: findings from the DIAGNOSE CTE Research Project. J Neuroinflammation 21, 46 (2024). https://doi.org/10.1186/s12974-024-03034-6Journal
Journal of NeuroinflammationRights
© The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Background: Traumatic encephalopathy syndrome (TES) is defined as the clinical manifestation of the neuropathological entity chronic traumatic encephalopathy (CTE). A core feature of TES is neurobehavioral dysregulation (NBD), a neuropsychiatric syndrome in repetitive head impact (RHI)-exposed individuals, characterized by a poor regulation of emotions/behavior. To discover biological correlates for NBD, we investigated the association between biomarkers of inflammation (interleukin (IL)-1β, IL-6, IL-8, IL-10, C-reactive protein (CRP), tumor necrosis factor (TNF)-α) in cerebrospinal fluid (CSF) and NBD symptoms in former American football players and unexposed individuals. Methods: Our cohort consisted of former American football players, with (n = 104) or without (n = 76) NBD diagnosis, as well as asymptomatic unexposed individuals (n = 55) from the DIAGNOSE CTE Research Project. Specific measures for NBD were derived (i.e., explosivity, emotional dyscontrol, impulsivity, affective lability, and a total NBD score) from a factor analysis of multiple self-report neuropsychiatric measures. Analyses of covariance tested differences in biomarker concentrations between the three groups. Within former football players, multivariable linear regression models assessed relationships among log-transformed inflammatory biomarkers, proxies for RHI exposure (total years of football, cumulative head impact index), and NBD factor scores, adjusted for relevant confounding variables. Sensitivity analyses tested (1) differences in age subgroups (< 60, ≥ 60 years); (2) whether associations could be identified with plasma inflammatory biomarkers; (3) associations between neurodegeneration and NBD, using plasma neurofilament light (NfL) chain protein; and (4) associations between biomarkers and cognitive performance to explore broader clinical symptoms related to TES. Results: CSF IL-6 was higher in former American football players with NBD diagnosis compared to players without NBD. Furthermore, elevated levels of CSF IL-6 were significantly associated with higher emotional dyscontrol, affective lability, impulsivity, and total NBD scores. In older football players, plasma NfL was associated with higher emotional dyscontrol and impulsivity, but also with worse executive function and processing speed. Proxies for RHI exposure were not significantly associated with biomarker concentrations. Conclusion: Specific NBD symptoms in former American football players may result from multiple factors, including neuroinflammation and neurodegeneration. Future studies need to unravel the exact link between NBD and RHI exposure, including the role of other pathophysiological pathways. © The Author(s) 2024.Note
Open access journalISSN
1742-2094PubMed ID
38336728Version
Final Published Versionae974a485f413a2113503eed53cd6c53
10.1186/s12974-024-03034-6
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Except where otherwise noted, this item's license is described as © The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License.
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