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Inflammatory biomarkers for neurobehavioral dysregulation in former American football players: findings from the DIAGNOSE CTE Research Project.
van Amerongen, Suzan; Pulukuri, Surya V; Tuz-Zahra, Fatima; Tripodis, Yorghos; Cherry, Jonathan D; Bernick, Charles; Geda, Yonas E; Wethe, Jennifer V; Katz, Douglas I; Alosco, Michael L; Adler, Charles H; Balcer, Laura J; Ashton, Nicholas J; Blennow, Kaj; Zetterberg, Henrik; Daneshvar, Daniel H; Colasurdo, Elizabeth A; Iliff, Jeffrey J; Li, Gail; Peskind, Elaine R; Shenton, Martha E; Reiman, Eric M; Cummings, Jeffrey L; Stern, Robert A.
Affiliation
  • van Amerongen S; Boston University CTE Center, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Pulukuri SV; Alzheimer Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC Location VUmc, Amsterdam, The Netherlands.
  • Tuz-Zahra F; Amsterdam Neuroscience, Neurodegeneration, Amsterdam, The Netherlands.
  • Tripodis Y; Boston University CTE Center, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Cherry JD; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
  • Bernick C; Boston University CTE Center, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Geda YE; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
  • Wethe JV; Boston University Alzheimer's Disease Research Center, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Katz DI; Boston University CTE Center, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Alosco ML; Boston University Alzheimer's Disease Research Center, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Adler CH; VA Boston Healthcare System, U.S. Department of Veteran Affairs, Boston, MA, USA.
  • Balcer LJ; Department of Veterans Affairs Medical Center, Bedford, MA, USA.
  • Ashton NJ; Department of Pathology and Laboratory Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Blennow K; Cleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas, NV, USA.
  • Zetterberg H; Department of Neurology and the Franke Global Neuroscience Education Center, Barrow Neurological Institute, Phoenix, AZ, USA.
  • Daneshvar DH; Department of Psychiatry and Psychology, Mayo Clinic School of Medicine, Mayo Clinic Arizona, Scottsdale, AZ, USA.
  • Colasurdo EA; Boston University CTE Center, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Iliff JJ; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Li G; Brain Injury Program, Encompass Health Braintree Rehabilitation Hospital, Braintree, MA, USA.
  • Peskind ER; Boston University CTE Center, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Shenton ME; Boston University Alzheimer's Disease Research Center, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Reiman EM; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Cummings JL; Department of Neurology, Mayo Clinic College of Medicine, Mayo Clinic Arizona, Scottsdale, AZ, USA.
  • Stern RA; Departments of Neurology, Population Health and Ophthalmology, NYU Grossman School of Medicine, New York, NY, USA.
J Neuroinflammation ; 21(1): 46, 2024 Feb 09.
Article in En | MEDLINE | ID: mdl-38336728
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)-1ß, 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Injuries, Traumatic / Chronic Traumatic Encephalopathy / Football Type of study: Diagnostic_studies / Prognostic_studies Limits: Aged / Humans / Middle aged Language: En Journal: J Neuroinflammation Journal subject: NEUROLOGIA Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Injuries, Traumatic / Chronic Traumatic Encephalopathy / Football Type of study: Diagnostic_studies / Prognostic_studies Limits: Aged / Humans / Middle aged Language: En Journal: J Neuroinflammation Journal subject: NEUROLOGIA Year: 2024 Document type: Article Affiliation country: