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Research paper
[18F]AV-1451 binding in vivo mirrors the expected distribution of TDP-43 pathology in the semantic variant of primary progressive aphasia
  1. W R Bevan-Jones1,
  2. Thomas E Cope2,
  3. P Simon Jones2,
  4. Luca Passamonti2,
  5. Young T Hong3,
  6. Tim D Fryer3,
  7. Robert Arnold1,
  8. Kieren S J Allinson4,
  9. Jonathan P Coles5,
  10. Franklin I Aigbirhio3,
  11. Karalyn Patterson2,6,
  12. John T O’Brien1,
  13. James B Rowe2,6
  1. 1 Department of Psychiatry, University of Cambridge, Cambridge, UK
  2. 2 Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK
  3. 3 Wolfson Brain Imaging Centre, University of Cambridge, Cambridge, UK
  4. 4 Department of Pathology, Addenbrooke’s Hospital, Cambridge, UK
  5. 5 Division of Anaesthesia, University of Cambridge, Cambridge, UK
  6. 6 Cognition and Brain Sciences Unit, Medical Research Council Cognition and Brain Sciences Unit, Cambridge, UK
  1. Correspondence to Dr W R Bevan-Jones, Department of Psychiatry, University of Cambridge, HerchelSmith Building, Cambridge Biomedical Campus, Hills Road, Cambridge CB20SZ, UK; wrb22{at}


Introduction Semantic dementia, including the semantic variant of primary progressive aphasia (svPPA), is strongly associated with TAR-DNA binding protein 43 (TDP-43) type C pathology. It provides a useful model in which to test the specificity of in vivo binding of the putative tau ligand [18F]AV-1451, which is elevated in frontotemporal lobar degeneration tauopathies.

Methods and results Seven patients (five with svPPA and two with ‘right’ semantic dementia) and 12 healthy controls underwent positron emission tomography brain imaging with [18F]AV-1451. Two independent preprocessing methods were used. For both methods, all patients had clearly elevated binding potential (BPND (non-displaceable binding potential)) in temporal lobes, lateralising according to their clinical syndrome and evident in raw images. Region of interest analyses confirmed that BPND was significantly increased in temporal regions, insula and fusiform gyrus, consistent with those areas known to be most affected in semantic dementia. Hierarchical cluster analysis, based on the distribution of [18F]AV-1451 binding potential, separated semantic dementia from controls with 86% sensitivity and 100% specificity.

Conclusions [18F]AV-1451 binds in vivo regions that are likely to contain TDP-43 and not significant tau pathology. While this suggests a non-tau target for [18F]AV-1451, the pathological regions in semantic dementia do not normally contain significant levels of recently proposed ‘off target’ binding sites for [18F]AV-1451, such as neuronal monoamine oxidase or neuromelanin. Postmortem and longitudinal data will be useful to assess the utility of [18F]AV-1451 to differentiate and track different types of frontotemporal lobar degeneration.

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  • JTO’B and JBR contributed equally.

  • Contributors Conceptualisation: JBR, JTOB and FIA; methodology: PSJ, TEC, JBR and WRBJ; investigation: WRBJ, LP, RA and KSJA; formal analysis: YTH, TDF, PSJ and TEC; resources: FIA, TDF, YTH and JPC. Writing: original draft: WRBJ; review and editing: TEC, PSJ, JBR, JTOB, LP and KP; funding acquisition: JBR and JTOB; supervision: JBR, JTOB, FIA and KP.

  • Funding This work was supported by the National Institute for Health Research Biomedical Research Centre and Biomedical Research Unit in Dementia; the Wellcome Trust (JBR 103838); the Association of British Neurologists and the Patrick Berthoud Charitable Trust (TEC).

  • Competing interests None declared.

  • Ethics approval NRES Committee East of EnglandCentral Cambridge.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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