Home > Journals > The Quarterly Journal of Nuclear Medicine and Molecular Imaging > Past Issues > The Quarterly Journal of Nuclear Medicine and Molecular Imaging 2017 December;61(4) > The Quarterly Journal of Nuclear Medicine and Molecular Imaging 2017 December;61(4):405-13

CURRENT ISSUE
 

JOURNAL TOOLS

Publishing options
eTOC
To subscribe
Submit an article
Recommend to your librarian
 

ARTICLE TOOLS

Publication history
Reprints
Permissions
Cite this article as
Share

 

REVIEW  NEWS AND VIEWS ON CLINICAL NEUROIMAGING 

The Quarterly Journal of Nuclear Medicine and Molecular Imaging 2017 December;61(4):405-13

DOI: 10.23736/S1824-4785.17.03012-6

Copyright © 2017 EDIZIONI MINERVA MEDICA

language: English

Tau imaging with PET: an overview of challenges, current progress, and future applications

Joanne S. ROBERTSON 1, Christopher C. ROWE 1, 2, 3, Victor L. VILLEMAGNE 1, 2, 3

1 The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Australia; 2 Department of Molecular Imaging and Therapy, Centre for PET, Austin Health, Heidelberg, Australia; 3 Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Australia


PDF


Folded and misfolded tau is common to many neurodegenerative conditions, collectively termed “tauopathies”. In recent years, many efforts have contributed toward development of tau imaging agents to allow measurement of tau deposits in vivo using positron emission tomography (PET). The particularities of tau present some unique challenges for the development of tau imaging tracers. Most notably, these pertain to the predominantly intracellular nature of tau aggregations, the existence of six isoforms, multiple post-translational modification, and that tau is usually surrounded by larger concentrations of Aβ plaques. Nevertheless, significant progress has been made towards overcoming these issues and a number of tracers are now undergoing human trials. Once validated, tau imaging with PET will be a useful tool for the differential diagnosis and disease staging, as well as therapeutic trials of AD and non-AD tauopathies.


KEY WORDS: Tauopathies - Positron-emission tomography - Nerve degeneration

top of page