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Visual assessment of [18F]flutemetamol PET images can detect early amyloid pathology and grade its extent

Authors :
Andrés Perissinotti
Gemma Salvadó
Milos D. Ikonomovic
Gill Farrar
Juhan Reimand
Mahnaz Shekari
Juan Domingo Gispert
Bart N.M. van Berckel
Philip Scheltens
Lyduine E. Collij
Frederik Barkhof
Adrian Smith
José Luis Molinuevo
Isadora Lopes Alves
Aida Niñerola-Baizán
Alle Meije Wink
Marissa D. Zwan
Christopher Buckley
Radiology and nuclear medicine
Neurology
Amsterdam Neuroscience - Brain Imaging
Amsterdam Neuroscience - Neurodegeneration
Amsterdam Neuroscience - Neuroinfection & -inflammation
Source :
Collij, L E, Salvado, G, Shekari, M, Alves, I L, Reimand, J, Wink, A M, Zwan, M, Ninerola-Baizan, A, Perissinotti, A, Scheltens, P, Ikonomovic, M D, Smith, A P L, Farrar, G, Molinuevo, J L, Barkhof, F, Buckley, C J, van Berckel, B N M & Gispert, J D 2021, ' Visual assessment of [18F]flutemetamol PET images can detect early amyloid pathology and grade its extent ', European Journal of Nuclear Medicine and Molecular Imaging, vol. 48, no. 7, pp. 2169-2182 . https://doi.org/10.1007/s00259-020-05174-2, https://doi.org/10.1007/s00259-020-05174-2, European Journal of Nuclear Medicine and Molecular Imaging, 48(7), 2169-2182. Springer Verlag, European Journal of Nuclear Medicine and Molecular Imaging

Abstract

Purpose: To investigate the sensitivity of visual read (VR) to detect early amyloid pathology and the overall utility of regional VR. Methods: [18F]Flutemetamol PET images of 497 subjects (ALFA+ N = 352; ADC N = 145) were included. Scans were visually assessed according to product guidelines, recording the number of positive regions (0-5) and a final negative/positive classification. Scans were quantified using the standard and regional Centiloid (CL) method. The agreement between VR-based classification and published CL-based cut-offs for early (CL = 12) and established (CL = 30) pathology was determined. An optimal CL cut-off maximizing Youden's index was derived. Global and regional CL quantification was compared to VR. Finally, 28 post-mortem cases from the [18F]flutemetamol phase III trial were included to assess the percentage agreement between VR and neuropathological classification of neuritic plaque density. Results: VR showed excellent agreement against CL = 12 (κ = .89, 95.2%) and CL = 30 (κ = .88, 95.4%) cut-offs. ROC analysis resulted in an optimal CL = 17 cut-off against VR (sensitivity = 97.9%, specificity = 97.8%). Each additional positive VR region corresponded to a clear increase in global CL. Regional VR was also associated with regional CL quantification. Compared to mCERADSOT-based classification (i.e., any region mCERADSOT > 1.5), VR was in agreement in 89.3% of cases, with 13 true negatives, 12 true positives, and 3 false positives (FP). Regional sparse-to-moderate neuritic and substantial diffuse Aβ plaque was observed in all FP cases. Regional VR was also associated with regional plaque density. Conclusion: VR is an appropriate method for assessing early amyloid pathology and that grading the extent of visual amyloid positivity could present clinical value. This project has received funding from the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement No 115952. This Joint Undertaking receives support from the European Union’s Horizon 2020 research and innovation programme and EFPIA. The ALFA Study is funded by “la Caixa” Foundation (LCF/PR/GN17/10300004) and the Alzheimer’s Association and an international anonymous charity foundation through the the TriBEKa Imaging Platform project (TriBEKa-17-519007). Additional funding has been obtained by Project RTI2018-102261-B-I00, funded by European Regional Development Fund (EDRF) / Ministry of Science and Innovation - State Research Agency (Spain). This work also received in kind sponsoring of the PET-tracer from GE Healthcare. FB is supported by the NIHR UCLH biomedical research centre. FB and AMW are supported by the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 666992.

Details

Language :
English
ISSN :
16197089 and 16197070
Volume :
48
Issue :
7
Database :
OpenAIRE
Journal :
European Journal of Nuclear Medicine and Molecular Imaging
Accession number :
edsair.doi.dedup.....e1a910c0624d7778d0cfd51bf4f58477
Full Text :
https://doi.org/10.1007/s00259-020-05174-2