Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25623
Title: Case Report: 18F-MK6240 Tau Positron Emission Tomography Pattern Resembling Chronic Traumatic Encephalopathy in a Retired Australian Rules Football Player.
Austin Authors: Krishnadas, Natasha ;Doré, Vincent ;Lamb, Fiona ;Groot, Colin;McCrory, Paul;Guzman, Rodney;Mulligan, Rachel S ;Huang, Kun ;O'Donnell, Meaghan;Ponsford, Jennie;Hopwood, Malcolm;Villemagne, Victor L ;Rowe, Christopher C 
Affiliation: Department of Neurology, Alzheimer Center Amsterdam, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam, Netherlands
Monash-Epworth Rehabilitation Centre, Turner Institute for Brain and Mental Health, Monash University, Clayton, VIC, Australia
Florey Department of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, Australia
Phoenix Australia, Parkville, VIC, Australia
The Department of Psychiatry, The University of Melbourne, Parkville, VIC, Australia
Molecular Imaging and Therapy
The Florey Institute of Neuroscience and Mental Health, Parkville, VIC, Australia
The Australian e-Health Research Centre, CSIRO Health & Biosecurity, Parkville, VIC, Australia
Issue Date: 22-Dec-2020
metadata.dc.date: 2020-12-22
Publication information: Frontiers in neurology 2020; 11: 598980
Abstract: Introduction: It remains unclear if tau imaging may assist diagnosis of chronic traumatic encephalopathy (CTE). Flortaucipir PET has shown superior frontal with medial temporal tau binding consistent with the provisional neuropathological criteria for mid-stage CTE in group-level analyses of retired symptomatic NFL players and in one individual with pathologically confirmed CTE. 18F-MK6240 is a new PET ligand that has high affinity for tau. We present the case of a 63-year-old cognitively impaired, former Australian rules football player with distinct superior frontal and medial temporal 18F-MK6240 binding and show it to be significantly different to the pattern seen in prodromal Alzheimer's disease (AD). Findings: The participant was recruited for a study of amyloid-β and tau several decades after traumatic brain injury. He had multiple concussions during his football career but no cognitive complaints at retirement. A thalamic stroke in his mid 50s left stable mild cognitive deficits but family members reported further short-term memory, behavioral, and personality decline preceding the study. Imaging showed extensive small vessel disease on MRI, a moderate burden of amyloid-β plaques, and 18F-MK6240 binding in bilateral superior frontal and medial temporal cortices. Voxel-wise analysis demonstrated that the frontally predominant pattern of the participant was significantly different to the posterior temporo-parietal predominant pattern of prodromal AD. Conclusion: Although lacking neuropathological examination to distinguish CTE from a variant of AD, the clear demonstration of a CTE-like tau pattern in a single at-risk individual suggests further research on the potential of 18F-MK6240 PET for identifying CTE is warranted.
URI: https://ahro.austin.org.au/austinjspui/handle/1/25623
DOI: 10.3389/fneur.2020.598980
PubMed URL: 33414760
ISSN: 1664-2295
Type: Journal Article
Subjects: Alzheimer's Disease (AD)
Chronic Traumatic Encephalopathy (CTE)
Positron Emission Tomography (PET)
case report
tau
Appears in Collections:Journal articles

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