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Characterization of tau positron emission tomography tracer [18F]AV-1451 binding to postmortem tissue in Alzheimer's disease, primary tauopathies, and other dementias.
Sander, Kerstin; Lashley, Tammaryn; Gami, Priya; Gendron, Thibault; Lythgoe, Mark F; Rohrer, Jonathan D; Schott, Jonathan M; Revesz, Tamas; Fox, Nick C; Årstad, Erik.
Affiliation
  • Sander K; Institute of Nuclear Medicine and Department of Chemistry, University College London, London, UK.
  • Lashley T; Institute of Neurology, Department of Molecular Neuroscience, Queen Square Brain Bank, University College London, London, UK.
  • Gami P; Institute of Neurology, Department of Molecular Neuroscience, Queen Square Brain Bank, University College London, London, UK.
  • Gendron T; Institute of Nuclear Medicine and Department of Chemistry, University College London, London, UK.
  • Lythgoe MF; Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, UK.
  • Rohrer JD; Institute of Neurology, Department of Neurodegenerative Disease, Dementia Research Centre, University College London, London, UK.
  • Schott JM; Institute of Neurology, Department of Neurodegenerative Disease, Dementia Research Centre, University College London, London, UK.
  • Revesz T; Institute of Neurology, Department of Molecular Neuroscience, Queen Square Brain Bank, University College London, London, UK.
  • Fox NC; Institute of Neurology, Department of Neurodegenerative Disease, Dementia Research Centre, University College London, London, UK.
  • Årstad E; Institute of Nuclear Medicine and Department of Chemistry, University College London, London, UK. Electronic address: e.arstad@ucl.ac.uk.
Alzheimers Dement ; 12(11): 1116-1124, 2016 11.
Article in En | MEDLINE | ID: mdl-26892233
ABSTRACT

INTRODUCTION:

Aggregation of tau is a hallmark of many neurodegenerative diseases, and tau imaging with positron emission tomography (PET) may allow early diagnosis and treatment monitoring. We assessed binding of the PET tracer [18F]AV-1451 in a range of dementias.

METHODS:

Phosphorimaging was used to quantify binding to postmortem brain tissue from 33 patients with different, histopathologically characterized, neurodegenerative dementias.

RESULTS:

[18F]AV-1451 showed high specific binding in cases with Alzheimer's disease (AD), moderate binding in Pick's disease and frontotemporal dementia with parkinsonism-17, and low but displaceable binding in corticobasal degeneration, progressive supranuclear palsy, non-tau proteinopathies, and in controls without pathology. Tracer binding did not correlate with tau load within disease groups.

DISCUSSION:

[18F]AV-1451 binds to tau in AD, and some other tauopathies. However, evidence for a non-tau binding site and lack of correlation between tracer binding and antibody staining suggest that reliable quantification of tau load with this tracer is problematic.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Brain / Carbolines / Radiopharmaceuticals / Neurodegenerative Diseases / Dementia / Positron-Emission Tomography Type of study: Screening_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Alzheimers Dement Year: 2016 Type: Article Affiliation country: United kingdom

Full text: 1 Database: MEDLINE Main subject: Brain / Carbolines / Radiopharmaceuticals / Neurodegenerative Diseases / Dementia / Positron-Emission Tomography Type of study: Screening_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Alzheimers Dement Year: 2016 Type: Article Affiliation country: United kingdom