Biomarkers of Neurobiologic Recovery in Adults With Sport-Related Concussion
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Published:2024-06-07
Issue:6
Volume:7
Page:e2415983
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ISSN:2574-3805
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Container-title:JAMA Network Open
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language:en
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Short-container-title:JAMA Netw Open
Author:
O’Brien William T.1, Spitz Gershon12, Xie Becca1, Major Brendan P.1, Mutimer Steven1, Giesler Lauren P.1, Bain Jesse1, Evans Lauren J.1, Duarte Martins Beatriz1, Piantella Stefan1, Alhassan Afizu1, Brady Shelby1, Cappellari David1, Somma Vincenzo1, McColl Thomas1, Symons Georgia F.1, Gore Tenae1, Sun Matthew1, Kuek Timothy1, Horan Seamus1, Bei Michael1, Ponsford Jennie L.2, Willmott Catherine23, Reyes Jonathan23, Ashton Nicholas J.4567, Zetterberg Henrik4891011, Mitra Biswadev1213, O’Brien Terence J.11415, Shultz Sandy R.11416, McDonald Stuart J.114
Affiliation:
1. Department of Neuroscience, Monash University, Melbourne, Victoria, Australia 2. Monash-Epworth Rehabilitation Research Centre, School of Psychological Sciences, Monash University, Melbourne, Victoria, Australia 3. Australian Football League, Melbourne, Victoria, Australia 4. Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden 5. King’s College London, Institute of Psychiatry, Psychology and Neuroscience, Maurice Wohl Institute Clinical Neuroscience Institute, London, United Kingdom 6. NIHR Biomedical Research Centre for Mental Health and Biomedical Research Unit for Dementia at South London and Maudsley NHS Foundation, London, United Kingdom 7. Centre for Age-Related Medicine, Stavanger University Hospital, Stavanger, Norway 8. Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden 9. Department of Neurodegenerative Disease, University College London Institute of Neurology, Queen Square, London, United Kingdom 10. UK Dementia Research Institute at University College London, London, United Kingdom 11. Hong Kong Center for Neurodegenerative Diseases, Hong Kong, Hong Kong SAR, China 12. Emergency & Trauma Centre, The Alfred Hospital, Australia 13. School of Public Health & Preventive Medicine, Monash University, Melbourne, Victoria, Australia 14. Department of Neurology, The Alfred Hospital, Melbourne, Victoria, Australia 15. Department of Medicine, Royal Melbourne Hospital, The University of Melbourne, Parkville, Victoria, Australia 16. Health Sciences, Vancouver Island University, Nanaimo, British Columbia, Canada
Abstract
ImportanceSport-related concussion (SRC), a form of mild traumatic brain injury, is a prevalent occurrence in collision sports. There are no well-established approaches for tracking neurobiologic recovery after SRC.ObjectiveTo examine the levels of serum glial fibrillary acidic protein (GFAP) and neurofilament light (NfL) in Australian football athletes who experience SRC.Design, Setting, and ParticipantsA cohort study recruiting from April 10, 2021, to September 17, 2022, was conducted through the Victorian Amateur Football Association, Melbourne, Australia. Participants included adult Australian football players with or without SRC. Data analysis was performed from May 26, 2023, to March 27, 2024.ExposureSport-related concussion, defined as at least 1 observable sign and/or 2 or more symptoms.Main Outcomes and MeasuresPrimary outcomes were serum GFAP and NfL levels at 24 hours, and 1, 2, 4, 6, 8, 12, and 26 weeks. Secondary outcomes were symptoms, cognitive performance, and return to training times.ResultsEighty-one individuals with SRC (median age, 22.8 [IQR, 21.3-26.0] years; 89% male) and 56 control individuals (median age, 24.6 [IQR, 22.4-27.3] years; 96% male) completed a total of 945 of 1057 eligible testing sessions. Compared with control participants, those with SRC exhibited higher GFAP levels at 24 hours (mean difference [MD] in natural log, pg/mL, 0.66 [95% CI, 0.50-0.82]) and 4 weeks (MD, 0.17 [95% CI, 0.02-0.32]), and NfL from 1 to 12 weeks (1-week MD, 0.31 [95% CI, 0.12-0.51]; 2-week MD, 0.38 [95% CI, 0.19-0.58]; 4-week MD, 0.31 [95% CI, 0.12-0.51]; 6-week MD, 0.27 [95% CI, 0.07-0.47]; 8-week MD, 0.36 [95% CI, 0.15-0.56]; and 12-week MD, 0.25 [95% CI, 0.04-0.46]). Growth mixture modeling identified 2 GFAP subgroups: extreme prolonged (16%) and moderate transient (84%). For NfL, 3 subgroups were identified: extreme prolonged (7%), moderate prolonged (15%), and minimal or no change (78%). Individuals with SRC who reported loss of consciousness (LOC) (33% of SRC cases) had higher GFAP at 24 hours (MD, 1.01 [95% CI, 0.77-1.24]), 1 week (MD, 0.27 [95% CI, 0.06-0.49]), 2 weeks (MD, 0.21 [95% CI, 0.004-0.42]) and 4 weeks (MD, 0.34 [95% CI, 0.13-0.55]), and higher NfL from 1 week to 12 weeks (1-week MD, 0.73 [95% CI, 0.42-1.03]; 2-week MD, 0.91 [95% CI, 0.61-1.21]; 4-week MD, 0.90 [95% CI, 0.59-1.20]; 6-week MD, 0.81 [95% CI, 0.50-1.13]; 8-week MD, 0.73 [95% CI, 0.42-1.04]; and 12-week MD, 0.54 [95% CI, 0.22-0.85]) compared with SRC participants without LOC. Return to training times were longer in the GFAP extreme compared with moderate subgroup (incident rate ratio [IRR], 1.99 [95% CI, 1.69-2.34]; NfL extreme (IRR, 3.24 [95% CI, 2.63-3.97]) and moderate (IRR, 1.43 [95% CI, 1.18-1.72]) subgroups compared with the minimal subgroup, and for individuals with LOC compared with those without LOC (IRR, 1.65 [95% CI, 1.41-1.93]).Conclusions and RelevanceIn this cohort study, a subset of SRC cases, particularly those with LOC, showed heightened and prolonged increases in GFAP and NfL levels, that persisted for at least 4 weeks. These findings suggest that serial biomarker measurement could identify such cases, guiding return to play decisions based on neurobiologic recovery. While further investigation is warranted, the association between prolonged biomarker elevations and LOC may support the use of more conservative return to play timelines for athletes with this clinical feature.
Publisher
American Medical Association (AMA)
Cited by
2 articles.
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