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. 2023 Jun 10;50(11):3276–3289. doi: 10.1007/s00259-023-06279-0

Table 1.

Description of the cohorts included in this retrospective analysis

Cohort Clinical data source Clinical diagnosis Objective for retrospective analysis Subset analysis Visual assessment
#1, n = 91 NCT01020838 [8, 9]

59 AD

4 DLB

9 DEM

19 NDV

To assess the sensitivity and specificity of quantification methods against the histopathological confirmation 3 expert blinded readers
To compare the diagnostic performance of quantification methods with previously established visual assessment performed by 3 expert blinded readers and 5 newly trained blinded readers 5 newly trained blinded readers
#2, n = 439 Images from clinical phase 1, 2, and 3 studies were visually assessed by five independent blinded readers in a pooled read study

183 eHC

169 AD

9 DLB

11 FTLD

1 FTD

51 MCI

5 PD

4 VaD

6 other

To assess the concordance between visual assessment performed by 5 blinded readers and binary quantitative assessment of FBB PET scans

To assess agreement and reliability between (inter-software) and within (intra-software) analytical methods

Subset 1 (n = 386): excluded subjects from cohort #1 used to generate the cut-off

Subset 2 (n = 439): represents the full sample

Subset 3 (n = 336): based on subset 2 and included only subjects with consensus among 5 independent blinded readers

Subset 4 (n = 84): randomly selected scans to assess intra-software reliability

5 newly trained blinded readers
#3, n = 45 NCT01138111 [28] 45 MCI

To assess the prognostic accuracy of quantitative assessment of amyloid-beta load using FBB PET for progression to AD

To assess the capacity of quantitative assessment of amyloid-beta load using FBB PET to detect longitudinal changes

#4, n = 35 Global Alzheimer’s Association Information Network (GAAIN) [29]

10 yHC

6 eHC

9 MCI

8 AD

2 FTD

To compare the results of FBB PET quantification against the quantitative results provided in a publicly available dataset

AD Alzheimer’s disease, DEM other dementia, DLB dementia with Lewy bodies, eHC elderly healthy control, FTD frontotemporal dementia, FTLD frontotemporal lobar degeneration, MCI amnestic mild cognitively impaired, NDV non-demented volunteer, PD Parkinson’s disease, VaD vascular dementia, yHC young healthy control