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Visual assessment of [18F]flutemetamol PET images can detect early amyloid pathology and grade its extent
- 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
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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.
- Subjects :
- Amyloid pathology
business.industry
Amyloid pet
General Medicine
amyloid PET
[18F]flutemetamol
3. Good health
030218 nuclear medicine & medical imaging
03 medical and health sciences
0302 clinical medicine
Sensitivity
Visual assessment
Clinical value
False positive paradox
Medicine
Regional visual read
Radiology, Nuclear Medicine and imaging
Centiloid
Nuclear medicine
business
True positive rate
030217 neurology & neurosurgery
Neuropathology
Subjects
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