Evidence map›Paper›PMID 42288852›Full record

ArticleAlzheimer's research & therapy2026

Cognitive, biomarker, and neuroimaging indices associated with traumatic encephalopathy syndrome across two independent athlete cohorts.

Brooke D Conway Kleven, Lung-Chang Chien, Dana Surwill, Michael L Alosco, Jennifer V Wethe, Yorghos Tripodis, Charles H Adler, Martha E Shenton, Ofer Pasternak, Douglas I Katz and 10 more

Abstract read
In one paragraph

Article in Alzheimer's research & therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Brooke D Conway KlevenDepartment of Epidemiology and Biostatistics, School of Public Health, University of Nevada Las Vegas, Las Vegas, NV, USA. brooke.conway-kleven@unlv.edu.
Lung-Chang ChienDepartment of Epidemiology and Biostatistics, School of Public Health, University of Nevada Las Vegas, Las Vegas, NV, USA.
Dana SurwillDepartment of Environmental and Global Health, School of Public Health, University of NevadaLas Vegas, Las Vegas, NV, USA.
Michael L AloscoDepartment of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Jennifer V WetheDepartment of Psychiatry and Psychology, Mayo Clinic School of Medicine and Science, Scottsdale, AZ, USA.
Yorghos TripodisBoston University Alzheimer's Disease Research Center, Boston, MA, USA.
Charles H AdlerDepartment of Neurology, Mayo Clinic School of Medicine and Science, Scottsdale, AZ, USA.
Martha E ShentonDepartment of Psychiatry and Radiology, Harvard Medical School, Boston, MA, USA.
Ofer PasternakDepartment of Psychiatry, Mass General Brigham, Harvard Medical School, Boston, MA, USA.
Douglas I KatzDepartment of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Elaine PeskindDepartment of Psychiatry and Behavioral Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Laura J BalcerDepartment of Neurology, Grossman School of Medicine, New York University, New York, NY, USA.
Inga K KoerteDepartment of Child and Adolescent Psychiatry, Psychosomatic and Psychotherapy, cBRAIN, Ludwig-Maximilians-Universität (LMU), Munich, Germany.
Jesse MezDepartment of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Eric M ReimanBanner Alzheimer's Institute, Phoenix, AZ, USA.
Robert C CantuBoston University Alzheimer's Disease Research Center, Boston, MA, USA.
Robert A SternDepartment of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Henrik ZetterbergDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Charles Bernick *Cleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas, NV, USA.
Jeffrey L Cummings *Department of Brain Health, Kirk Kerkorian School of Medicine, University of Nevada Las Vegas, Las Vegas, NV, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTraumatic encephalopathy syndrome (TES) is a clinical research construct used to identify individuals at risk for chronic traumatic encephalopathy (CTE) following exposure to repetitive head impacts (RHI). Adjudication of TES relies on clinical features such as progressive cognitive impairment and neurobehavioral dysregulation. Blood-based biomarkers and structural neuroimaging abnormalities have been associated with TES but are not part of the criteria. This study evaluated whether TES identification was associated with the combined contribution of cognitive performance, blood biomarkers, and structural neuroimaging measures across two well-characterized cohorts.

methodsParticipants included 158 professional fighters from the Professional Athletes Brain Health Study and 149 former American football players from The DIAGNOSE CTE Research Project. Three indices were constructed representing complementary domains: a cognitive index reflecting cohort-specific cognitive features, a blood biomarker index including plasma neurofilament light chain, glial fibrillary acidic protein, total tau, tau phosphorylated at amino acid 231, and APOE-ε4 carrier status, and an imaging index comprising volumetric MRI measures of subcortical structures, ventricles, and corpus callosum subregions. Grouped weighted quantile sum regression models were estimated within each cohort to evaluate associations between these indices and TES while adjusting for age, race, competition status, and RHI exposure.

resultsMultidomain models demonstrated improved model performance compared with single-domain models in both cohorts (PABHS: AUC = 0.91, PPV = 0.80; DIAGNOSE CTE: AUC = 0.84, PPV = 0.85). Biomarker and imaging indices contributed additional information across cohorts, although imaging contributions were more prominent in fighters whereas blood biomarker associations were stronger in football players.

conclusionTES in RHI-exposed athletes was associated with a convergent clinicobiological profile observed across two independent cohorts with distinct exposure patterns. These findings support multidomain analytic frameworks for evaluating correlated biological signals in RHI-exposed populations and may inform future studies of TES and CTE.

Indexed as

AthletesBrainChronic Traumatic EncephalopathyCognitionAdultAthletic InjuriesBiomarkersCohort StudiesFootballHumansMagnetic Resonance ImagingMaleNeurofilament ProteinsNeuroimagingNeuropsychological Teststau ProteinsBiomarkersNeurofilament Proteinstau ProteinsBlood biomarkersChronic traumatic encephalopathyNeurodegenerationNeuroimagingRepetitive head impactsTraumatic encephalopathy syndrome

Identifiers

PMID42288852
PMCPMC13495526

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.