The Amyloid Imaging for the Prevention of Alzheimer's Disease Consortium: A European collaboration with a global impact
Creators
- Lyduine Collij1
- Gill Farrar2
- David Valléz García1
- Ilona Bader1
- Mahnaz Shekari3
- Luigi Lorenzini1
- Hugh Pemberton4
- Daniele Altomare5
- Sandra Pla6
- Mery Loor6
- Pawel Markiewicz4
- Maqsood Yaqub7
- Christopher Buckley2
- Giovanni B. Frisoni5
- Agneta Nordberg8
- Pierre Payoux9
- Andrew Stephens10
- Rossella Gismondi10
- Pieter Jelle Visser7
- Lisa Ford11
- Mark Schmidt11
- Cindy Birck12
- Jean Georges12
- Anja Mett2
- Zuzana Walker4
- Mercé Boada13
- Alexander Drzezga14
- Rik Vandenberghe15
- Bernard Hanseeuw16
- Frank Jessen14
- Michael Schöll17
- Craig Ritchie18
- Isadora Lopes Alves19
- Juan Domingo Gispert3
- Frederik Barkhof20
- on behalf of the AMYPAD consortium
- 1. Department of Radiology and Nuclear Medicine, Amsterdam University Medical Center, location VUmc, Amsterdam, Netherlands; Amsterdam Neuroscience, Brain Imaging, Amsterdam, Netherlands
- 2. GE Healthcare, Amersham, United Kingdom
- 3. arcelona Beta Brain Research Center, Barcelona, Spain
- 4. Centre for Medical Image Computing, and Queen Square Institute of Neurology, UCL, London, United Kingdom
- 5. Laboratory of Neuroimaging of Aging (LANVIE), Université de Genève, Geneva, Switzerland,
- 6. Synapse Research Management Partners, Barcelona, Spain,
- 7. Department of Radiology and Nuclear Medicine, Amsterdam University Medical Center, location VUmc, Amsterdam, Netherlands
- 8. Department of Neurobiology, Care Sciences and Society, Center of Alzheimer Research, Karolinska Institutet, Stockholm, Sweden
- 9. Department of Nuclear Medicine, Centre Hospitalier Universitaire de Toulouse, Toulouse, France,
- 10. ife Molecular Imaging GmbH, Berlin, Baden-Württemberg, Germany,
- 11. Janssen Pharmaceutica NV, Beerse, Belgium
- 12. Alzheimer Europe
- 13. Barcelona Alzheimer Treatment and Research Center Memory Clinic, Fundació ACE, Barcelona, Catalonia, Spain
- 14. Department of Psychiatry, University Hospital of Cologne, Cologne, North Rhine-Westphalia, Germany
- 15. Faculty of Medicine, University Hospitals Leuven, Leuven, Brussels, Belgium
- 16. Institute of Neuroscience (IONS), Université Catholique de Louvain, Brussels, Belgium
- 17. Department of Psychiatry and Neurochemistry, University of Gothenburg, Gothenburg, Sweden
- 18. Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland, United Kingdom
- 19. Brain Research Center, Amsterdam, Netherlands
- 20. Department of Radiology and Nuclear Medicine, Amsterdam University Medical Center, location VUmc, Amsterdam, Netherlands; Amsterdam Neuroscience, Brain Imaging, Amsterdam, Netherlands; Centre for Medical Image Computing, and Queen Square Institute of Neurology, UCL, London, United Kingdom
Description
Abstract:
Background: Amyloid-β (Aβ) accumulation is considered the earliest pathological change in Alzheimer’s disease (AD). The Amyloid Imaging to Prevent Alzheimer’s Disease (AMYPAD) consortium is a collaborative European framework across European Federation of Pharmaceutical Industries Associations (EFPIA), academic, and ‘Small and Medium-sized enterprises’ (SME) partners aiming to provide evidence on the clinical utility and cost-effectiveness of Positron Emission Tomography (PET) imaging in diagnostic work-up of AD and to support clinical trial design by developing optimal quantitative methodology in an early AD population. The AMYPAD studies: In the Diagnostic and Patient Management Study (DPMS), 844 participants from eight centres across three clinical subgroups (245 subjective cognitive decline, 342 mild cognitive impairment, and 258 dementia) were included. The Prognostic and Natural History Study (PNHS) recruited pre-dementia subjects across 11 European parent cohorts (PCs). Approximately 1600 unique subjects with historical and prospective data were collected within this study. PET acquisition with [18F]flutemetamol or [18F]florbetaben radiotracers was performed and quantified using the Centiloid (CL) method.
Results: AMYPAD has significantly contributed to the AD field by furthering our understanding of amyloid deposition in the brain and the optimal methodology to measure this process. Main contributions so far include the validation of the dual-time window acquisition protocol to derive the fully quantitative non-displaceable binding potential (BPND), assess the value of this metric in the context of clinical trials, improve PET-sensitivity to emerging Aβ burden and utilize its available regional information, establish the quantitative accuracy of the Centiloid method across tracers and support implementation of quantitative amyloid-PET measures in the clinical routine.
Future steps: The AMYPAD consortium has succeeded in recruiting and following a large number of prospective subjects and setting up a collaborative framework to integrate data across European PCs. Efforts are currently ongoing in collaboration with ARIDHIA and ADDI to harmonize, integrate, and curate all available clinical data from the PNHS PCs, which will become openly accessible to the wider scientific community.
Notes
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