Evidence map›Paper›PMID 39414174›Full record

ArticleBrain, behavior, and immunity2025

Association of concussion history with psychiatric symptoms, limbic system structure, and kynurenine pathway metabolites in healthy, collegiate-aged athletes.

Timothy B Meier, Jonathan Savitz, Lezlie Y España, Bryna D Goeckner, T Kent Teague, Harm Jan van der Horn, L Tugan Muftuler, Andrew R Mayer, Benjamin L Brett

Abstract read
In one paragraph

Article in Brain, behavior, and immunity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Timothy B MeierDepartment of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, the United States of America; Department of Biomedical Engineering, Medical College of Wisconsin, Milwaukee, WI, the United States of America; Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, the United States of America. Electronic address: tmeier@mcw.edu.
Jonathan SavitzLaureate Institute for Brain Research, Tulsa, OK 74136, the United States of America; Oxley College of Health Sciences, The University of Tulsa, Tulsa, OK 74119, the United States of America.
Lezlie Y EspañaDepartment of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, the United States of America.
Bryna D GoecknerDepartment of Biophysics, Medical College of Wisconsin, Milwaukee, WI, the United States of America.
T Kent TeagueDepartment of Psychiatry, The University of Oklahoma School of Community Medicine, Tulsa, OK 74135, the United States of America; Department of Surgery, The University of Oklahoma School of Community Medicine, Tulsa, OK 74135, the United States of America; Department of Pharmaceutical Sciences, University of Oklahoma College of Pharmacy, Tulsa, OK 74135, the United States of America.
Harm Jan van der HornThe Mind Research Network/Lovelace Biomedical and Environmental Research Institute, Albuquerque, NM, the United States of America; University of Groningen, University Medical Center Groningen, the Netherlands.
L Tugan MuftulerDepartment of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, the United States of America.
Andrew R MayerThe Mind Research Network/Lovelace Biomedical and Environmental Research Institute, Albuquerque, NM, the United States of America; Departments of Neurology and Psychiatry, University of New Mexico School of Medicine, Albuquerque, NM, the United States of America; Department of Psychology, University of New Mexico, Albuquerque, NM, the United States of America.
Benjamin L BrettDepartment of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, the United States of America; Department of Neurology, Medical College of Wisconsin, Milwaukee, WI, the United States of America.

Funding

Clinical and Translational Science AwardUL1TR001436 · NCATS · MEDICAL COLLEGE OF WISCONSIN · PI FREED, JULIE K · 2015 to 2025
$47.5M
The role of neuroactive kynurenine metabolites in the chronic sequelae of concussion and contact sport exposureR01NS102225 · NINDS · MEDICAL COLLEGE OF WISCONSIN · PI MEIER, TIMOTHY B. · 2018 to 2022
$1.8M
The effects of cumulative concussion, repetitive head impacts, and comorbid cardiovascular risk factors on MRI metrics of pathological aging and neurobehavioral functioning across the lifespanK23AG073528 · NIA · MEDICAL COLLEGE OF WISCONSIN · PI BRETT, BENJAMIN L · 2021 to 2025
$661k
NCATS NIH HHS UL1 TR001436NIA NIH HHS K23 AG073528NINDS NIH HHS L30 NS113158NINDS NIH HHS R01 NS102225
6 · The paper itself

Abstract

Psychiatric outcomes are commonly observed in individuals with repeated concussions, though their underlying mechanism is unknown. One potential mechanism linking concussion with psychiatric symptoms is inflammation-induced activation of the kynurenine pathway, which is thought to play a role in the pathogenesis of mood disorders. Here, we investigated the association of prior concussion with multiple psychiatric-related outcomes in otherwise healthy male and female collegiate-aged athletes (N = 212) with varying histories of concussion recruited from the community. Specially, we tested the hypotheses that concussion history is associated with worse psychiatric symptoms, limbic system structural abnormalities (hippocampal volume, white matter microstructure assessed using neurite orientation dispersion and density imaging; NODDI), and elevations in kynurenine pathway (KP) metabolites (e.g., Quinolinic acid; QuinA). Given known sex-effects on concussion risk and recovery, psychiatric outcomes, and the kynurenine pathway, the moderating effect of sex was considered for all analyses. More concussions were associated with greater depression, anxiety, and anhedonia symptoms in female athletes (ps ≤ 0.005) and greater depression symptoms in male athletes (p = 0.011). More concussions were associated with smaller bilateral hippocampal tail (ps < 0.010) and left hippocampal body (p < 0.001) volumes across male and female athletes. Prior concussion was also associated with elevations in the orientation dispersion index (ODI) and lower intracellular volume fraction in several white matter tracts including the in uncinate fasciculus, cingulum-gyrus, and forceps major and minor, with evidence of female-specific associations in select regions. Regarding serum KP metabolites, more concussions were associated with elevated QuinA in females and lower tryptophan in males (ps ≤ 0.010). Finally, serum levels of QuinA were associated with elevated ODI (male and female athletes) and worse anxiety symptoms (females only), while higher ODI in female athletes and smaller hippocampal volumes in male athletes were associated with more severe anxiety and depression symptoms (ps ≤ 0.05). These data suggest that cumulative concussion is associated with psychiatric symptoms and limbic system structure in healthy athletes, with increased susceptibility to these effects in female athletes. Moreover, the associations of outcomes with serum KP metabolites highlight the KP as one potential molecular pathway underlying these observations.

Indexed as

AthletesBrain ConcussionDepressionHippocampusKynurenineLimbic SystemWhite MatterAdolescentAdultAnhedoniaAnxietyAthletic InjuriesFemaleHumansMagnetic Resonance ImagingMaleKynurenineQuinolinic AcidDepressiondiffusion MRIHippocampusMild traumatic brain injuryQuinolinic acidSport

Identifiers

PMID39414174
PMCPMC11624060

What OpenQuestion holds

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Registered trials

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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.