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Published in: European Journal of Nuclear Medicine and Molecular Imaging 10/2022

Open Access 07-04-2022 | Alzheimer's Disease | Review Article

Quantification of amyloid PET for future clinical use: a state-of-the-art review

Authors: Hugh G. Pemberton, Lyduine E. Collij, Fiona Heeman, Ariane Bollack, Mahnaz Shekari, Gemma Salvadó, Isadora Lopes Alves, David Vallez Garcia, Mark Battle, Christopher Buckley, Andrew W. Stephens, Santiago Bullich, Valentina Garibotto, Frederik Barkhof, Juan Domingo Gispert, Gill Farrar, on behalf of the AMYPAD consortium

Published in: European Journal of Nuclear Medicine and Molecular Imaging | Issue 10/2022

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Abstract

Amyloid-β (Aβ) pathology is one of the earliest detectable brain changes in Alzheimer’s disease (AD) pathogenesis. The overall load and spatial distribution of brain Aβ can be determined in vivo using positron emission tomography (PET), for which three fluorine-18 labelled radiotracers have been approved for clinical use. In clinical practice, trained readers will categorise scans as either Aβ positive or negative, based on visual inspection. Diagnostic decisions are often based on these reads and patient selection for clinical trials is increasingly guided by amyloid status. However, tracer deposition in the grey matter as a function of amyloid load is an inherently continuous process, which is not sufficiently appreciated through binary cut-offs alone. State-of-the-art methods for amyloid PET quantification can generate tracer-independent measures of Aβ burden. Recent research has shown the ability of these quantitative measures to highlight pathological changes at the earliest stages of the AD continuum and generate more sensitive thresholds, as well as improving diagnostic confidence around established binary cut-offs. With the recent FDA approval of aducanumab and more candidate drugs on the horizon, early identification of amyloid burden using quantitative measures is critical for enrolling appropriate subjects to help establish the optimal window for therapeutic intervention and secondary prevention. In addition, quantitative amyloid measurements are used for treatment response monitoring in clinical trials. In clinical settings, large multi-centre studies have shown that amyloid PET results change both diagnosis and patient management and that quantification can accurately predict rates of cognitive decline. Whether these changes in management reflect an improvement in clinical outcomes is yet to be determined and further validation work is required to establish the utility of quantification for supporting treatment endpoint decisions. In this state-of-the-art review, several tools and measures available for amyloid PET quantification are summarised and discussed. Use of these methods is growing both clinically and in the research domain. Concurrently, there is a duty of care to the wider dementia community to increase visibility and understanding of these methods.
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Metadata
Title
Quantification of amyloid PET for future clinical use: a state-of-the-art review
Authors
Hugh G. Pemberton
Lyduine E. Collij
Fiona Heeman
Ariane Bollack
Mahnaz Shekari
Gemma Salvadó
Isadora Lopes Alves
David Vallez Garcia
Mark Battle
Christopher Buckley
Andrew W. Stephens
Santiago Bullich
Valentina Garibotto
Frederik Barkhof
Juan Domingo Gispert
Gill Farrar
on behalf of the AMYPAD consortium
Publication date
07-04-2022
Publisher
Springer Berlin Heidelberg
Published in
European Journal of Nuclear Medicine and Molecular Imaging / Issue 10/2022
Print ISSN: 1619-7070
Electronic ISSN: 1619-7089
DOI
https://doi.org/10.1007/s00259-022-05784-y

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