Neuropsychological profiles and behavioural correlates in individuals exposed to repetitive head impacts: findings from the NEwTON study
4 affiliations
- 1Alzheimer Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc, Amsterdam, the Netherlands
- 2Amsterdam Neuroscience, Neurodegeneration, Amsterdam, the Netherlands
- 3Department of Clinical, Neuro- and Developmental Psychology, VU University, Amsterdam, the Netherlands
- 4Dementia Fund, EQT Life Sciences, Amsterdam, the Netherlands
Abstract
Background: Repetitive head impacts (RHI) are associated with an increased risk of neurodegenerative disease, most notably chronic traumatic encephalopathy (CTE). This study characterized neuropsychological profiles of RHI-exposed individuals compared to unexposed controls. To investigate whether cognitive dysfunction is linked to behavioural symptoms in RHI, we examined associations between executive functioning, social cognition and behavioural disinhibition.
Methods: We included RHI-exposed individuals (N = 72, 90.4% male, mean age 53.84 ± 12.45) and unexposed, cognitively healthy controls (N = 40, 82.5% male, mean age 54.55 ± 12.12) from the “Neurodegeneration: Traumatic brain injury as the Origin of Neuropathology” (NEwTON) study from Amsterdam UMC. Neurocognitive functioning was assessed through a comprehensive test battery covering episodic memory, attention and processing speed, executive functioning, visuospatial abilities, language and semantic memory, and social cognition. Behavioural disinhibition was measured in the RHI group using informant-based questionnaires (the positive items of the Frontal Behavioural Inventory (FBI) and the Neuropsychiatric Inventory (NPI)). Group differences in cognitive domains were assessed with analysis of covariance (ANCOVA) corrected for age, sex and education. The RHI-exposed group was evaluated for Traumatic Encephalopathy Syndrome (TES) criteria (No TES, Suggestive of CTE, Possible CTE, Probable CTE), TES subgroups were exploratively compared on cognitive performance. Associations between behavioural disinhibition and executive functioning or social cognition were assessed with regression analyses.
Results: RHI-exposed individuals performed worse on episodic memory (η2 = 0.12, pFDR ≤ .001), language and semantic memory (η2 = 0.10, pFDR = .001), executive functioning (η2 = 0.04, pFDR = .046), and social cognition (η2 = 0.04, pFDR = .040). No differences were found for visuospatial abilities (η2 = 0.01, pFDR = .221) and, although borderline significant, attention and processing speed (η2 = 0.03, pFDR = .074). Greater TES severity was associated with poorer performance on all cognitive domains. No significant associations were found between executive function or social cognition and behavioural disinhibition, as measured with the NPI and the FBI positive subscale (all p > .05).
Conclusions: RHI-exposed individuals showed poorer cognitive performance across several domains (episodic memory, executive functioning, social cognition and language and semantic memory). We found no association between cognitive function and behavioural disinhibition. Further longitudinal studies employing neuroimaging and biomarker data are needed to disentangle the underlying pathology in populations at risk for CTE.
Supplementary Information: The online version contains supplementary material available at https://doi.org/10.1186/s13195-026-02122-4.
Related
- Neuropsychological and behavioral correlates of cognitive function in patients with cerebral small vessel disease
- Symptoms as Correlates of Health-Related Quality of Life in Black and White Individuals With Multiple Sclerosis
- Intentions to abstain from alcohol during the Buddhist Lent campaign in Thailand: AUDIT-C risk profiles and independent sociodemographic correlates
- Behavioural influences on oral health status among individuals with schizophrenia: a cross-sectional study.
- Short-term thromboembolism risk and coagulation profiles among Thai transmasculine individuals receiving testosterone therapy: a quasi-experimental study
BibTeX
@article{kamps2026neuropsychological,
title = {{Neuropsychological profiles and behavioural correlates in individuals exposed to repetitive head impacts: findings from the NEwTON study}},
author = {Suzie Kamps and Esmé H. J. Habraken and Suzan van Amerongen and Dirk N. van Paassen and Sterre C. M. de Boer and Emma M. Coomans and Sietske A. M. Sikkes and Philip Scheltens and Rik Ossenkoppele and Everard G. B. Vijverberg},
journal = {Alzheimer's Research \& Therapy},
year = {2026},
month = jul,
doi = {10.1186/s13195-026-02122-4},
url = {https://doi.org/10.1186/s13195-026-02122-4},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Neuropsychological profiles and behavioural correlates in individuals exposed to repetitive head impacts: findings from the NEwTON study
AU - Suzie Kamps
AU - Esmé H. J. Habraken
AU - Suzan van Amerongen
AU - Dirk N. van Paassen
AU - Sterre C. M. de Boer
AU - Emma M. Coomans
AU - Sietske A. M. Sikkes
AU - Philip Scheltens
AU - Rik Ossenkoppele
AU - Everard G. B. Vijverberg
PY - 2026
DA - 2026/07/29
JO - Alzheimer's Research & Therapy
DO - 10.1186/s13195-026-02122-4
UR - https://doi.org/10.1186/s13195-026-02122-4
AB - Background: Repetitive head impacts (RHI) are associated with an increased risk of neurodegenerative disease, most notably chronic traumatic encephalopathy (CTE). This study characterized neuropsychological profiles of RHI-exposed individuals compared to unexposed controls. To investigate whether cognitive dysfunction is linked to behavioural symptoms in RHI, we examined associations between executive functioning, social cognition and behavioural disinhibition. Methods: We included RHI-exposed individuals (N = 72, 90.4% male, mean age 53.84 ± 12.45) and unexposed, cognitively healthy controls (N = 40, 82.5% male, mean age 54.55 ± 12.12) from the “Neurodegeneration: Traumatic brain injury as the Origin of Neuropathology” (NEwTON) study from Amsterdam UMC. Neurocognitive functioning was assessed through a comprehensive test battery covering episodic memory, attention and processing speed, executive functioning, visuospatial abilities, language and semantic memory, and social cognition. Behavioural disinhibition was measured in the RHI group using informant-based questionnaires (the positive items of the Frontal Behavioural Inventory (FBI) and the Neuropsychiatric Inventory (NPI)). Group differences in cognitive domains were assessed with analysis of covariance (ANCOVA) corrected for age, sex and education. The RHI-exposed group was evaluated for Traumatic Encephalopathy Syndrome (TES) criteria (No TES, Suggestive of CTE, Possible CTE, Probable CTE), TES subgroups were exploratively compared on cognitive performance. Associations between behavioural disinhibition and executive functioning or social cognition were assessed with regression analyses. Results: RHI-exposed individuals performed worse on episodic memory (η2 = 0.12, pFDR ≤ .001), language and semantic memory (η2 = 0.10, pFDR = .001), executive functioning (η2 = 0.04, pFDR = .046), and social cognition (η2 = 0.04, pFDR = .040). No differences were found for visuospatial abilities (η2 = 0.01, pFDR = .221) and, although borderline significant, attention and processing speed (η2 = 0.03, pFDR = .074). Greater TES severity was associated with poorer performance on all cognitive domains. No significant associations were found between executive function or social cognition and behavioural disinhibition, as measured with the NPI and the FBI positive subscale (all p > .05). Conclusions: RHI-exposed individuals showed poorer cognitive performance across several domains (episodic memory, executive functioning, social cognition and language and semantic memory). We found no association between cognitive function and behavioural disinhibition. Further longitudinal studies employing neuroimaging and biomarker data are needed to disentangle the underlying pathology in populations at risk for CTE. Supplementary Information: The online version contains supplementary material available at https://doi.org/10.1186/s13195-026-02122-4.
SN - 1758-9193
ER -