18F-Flortaucipir (AV1451) imaging identifies grey matter atrophy in retired athletes.
Athletes
Chronic traumatic encephalopathy
Concussion
Neurodegeneration
Pet
Tau
Journal
Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161
Informations de publication
Date de publication:
22 Jul 2024
22 Jul 2024
Historique:
received:
10
03
2024
accepted:
07
07
2024
revised:
06
06
2024
medline:
22
7
2024
pubmed:
22
7
2024
entrez:
22
7
2024
Statut:
aheadofprint
Résumé
The long-term consequences of concussions may include pathological neurodegeneration as seen in Alzheimer's disease (AD) and chronic traumatic encephalopathy (CTE). Tau-PET showed promise as a method to detect tau pathology of CTE, but more studies are needed OBJECTIVE: This study aimed (1) to assess the association of imaging evidence of tau pathology with brain volumes in retired athletes and (2) to examine the relationship between tau-PET and neuropsychological functioning. Former contact sport athletes were recruited through the Canadian Football League Alumni Association or the Canadian Concussion Centre clinic. Athletes completed MRI, [ 47 retired contact sport athletes negative for AD (age:51 ± 14; concussions/athlete:15 ± 2) and 54 normal controls (age:50 ± 13) were included. Tau-PET positive voxels had significantly lower GM volumes, compared to tau-PET negative voxels (- 0.37 ± 0.41 vs. - 0.31 ± 0.37, paired p = .006). There was a significant relationship between GM tau-PET % positivity and memory composite score (r = - .366, p = .02), controlled for age, PET scanner, and PET scan duration. There was no relationship between tau-PET measures and concussion number, or years of sport played. A higher tau-PET signal was associated with reduced GM volumes and lower memory scores. Tau-PET may be useful for identifying those at risk for neurodegeneration.
Sections du résumé
BACKGROUND
BACKGROUND
The long-term consequences of concussions may include pathological neurodegeneration as seen in Alzheimer's disease (AD) and chronic traumatic encephalopathy (CTE). Tau-PET showed promise as a method to detect tau pathology of CTE, but more studies are needed OBJECTIVE: This study aimed (1) to assess the association of imaging evidence of tau pathology with brain volumes in retired athletes and (2) to examine the relationship between tau-PET and neuropsychological functioning.
METHODS
METHODS
Former contact sport athletes were recruited through the Canadian Football League Alumni Association or the Canadian Concussion Centre clinic. Athletes completed MRI, [
RESULTS
RESULTS
47 retired contact sport athletes negative for AD (age:51 ± 14; concussions/athlete:15 ± 2) and 54 normal controls (age:50 ± 13) were included. Tau-PET positive voxels had significantly lower GM volumes, compared to tau-PET negative voxels (- 0.37 ± 0.41 vs. - 0.31 ± 0.37, paired p = .006). There was a significant relationship between GM tau-PET % positivity and memory composite score (r = - .366, p = .02), controlled for age, PET scanner, and PET scan duration. There was no relationship between tau-PET measures and concussion number, or years of sport played.
CONCLUSION
CONCLUSIONS
A higher tau-PET signal was associated with reduced GM volumes and lower memory scores. Tau-PET may be useful for identifying those at risk for neurodegeneration.
Identifiants
pubmed: 39037476
doi: 10.1007/s00415-024-12573-0
pii: 10.1007/s00415-024-12573-0
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Swedish Research Council
ID : #2022-01018
Organisme : Swedish Research Council
ID : #2019-02397
Organisme : Swedish Research Council
ID : 2017-00915
Organisme : Swedish State Support for Clinical Research
ID : ALFGBG-71320
Organisme : Alzheimer's Drug Discovery Foundation
ID : 201809-2016862
Organisme : Alzheimer's Drug Discovery Foundation
ID : RDAPB-201809-2016615
Organisme : AD Strategic Fund and the Alzheimer's Association
ID : #ADSF-21-831376-C
Organisme : AD Strategic Fund and the Alzheimer's Association
ID : #ADSF-21-831381-C
Organisme : AD Strategic Fund and the Alzheimer's Association
ID : #ADSF-21-831377-C
Organisme : Hjärnfonden
ID : FO2022-0270
Organisme : Hjärnfonden
ID : FO2017-0243
Organisme : European Union Joint Programme - Neurodegenerative Disease Research
ID : JPND2021-00694
Organisme : UK Dementia Research Institute at UCL
ID : UKDRI-1003
Organisme : Swedish Alzheimer Foundation
ID : AF-742881
Organisme : Swedish Alzheimer Foundation
ID : AF-930627
Organisme : ALF-agreement
ID : ALFGBG-715986
Organisme : European Union Joint Program for Neurodegenerative Disorders
ID : JPND2019-466-236
Organisme : National Institute of Health (NIH)
ID : 1R01AG068398-01
Organisme : BrightFocus Foundation
ID : A2020812F
Organisme : Swedish Brain Foundation
ID : FO2020-0240
Organisme : Agneta Prytz-Folkes & Gösta Folkes Foundation
ID : 2020-00124
Informations de copyright
© 2024. The Author(s).
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