Table 1.
Threshold derivation study |
Threshold validation study | ||
---|---|---|---|
Young adults | Older adults | Older adults | |
n | 18 | 154 | 50 |
Male (%) | 8 (44%) | 69 (45%) | 33 (66%) |
Age at PET | 23.7 (2.9) | 76.0 (6.2) | 69.8 (9.6) |
Education | 13.2 (6.2) | 16.1 (2.5) | 15.7 (2.9) |
MMSE | – | 28.9 (1.2) | 21.6 (6.8) |
ApoE4 (%) | 7 (47%)a | 45 (31%)b | 13 (27%)c |
CDR | – | – | 1.2 (0.8) |
Time from PET to death (years) | – | – | 3.1 (1.8) |
PiB index DVR | 1.01 (.03) | 1.12 (.20) | 1.14 (.29)d |
PiB+ (%), DVR cut-off 1.08 | 0 (0%) | 57 (37%) | 18 (40%)d |
PiB+ (%), DVR cut-off 1.20 | 0 (0%) | 34 (22%) | 13 (29%)d |
Clinical diagnosis at PET | Normal (18) | Normal (154) | FTDe (28), AD (11), MCI (7), AD/SIVD (1), DLB (1), normal (2) |
Primary neuropathological diagnosis | – | – | FTLDf (25), AD (6), CVD (6), AD/CVD (3), AD/DLB (3), AD/FTLD (4), TPD (1), AGD (1), no pathological findings (1) |
CERAD (absent, sparse, moderate, frequent) | – | – | 18, 8, 4, 20 |
Shown are mean (SD) unless specified otherwise.
aThree subjects were not genotyped.
bEight subjects were not genotyped.
cTwo subjects were not genotyped.
dDVR data missing for five subjects.
eClinical syndromes included: corticobasal syndrome (CBS; 8), behavioural-variant FTD (6), FTD and amyotrophic lateral sclerosis (5), non-fluent variant primary progressive aphasia (nfvPPA; 5), nfvPPA/CBS (1), semantic variant PPA (3).
fFTLD neuropathological subtypes: FTLD-TDP (12), corticobasal degeneration (7), Pick’s disease (3), progressive supranuclear palsy (2), FTLD with non-specific 4-repeat tauopathy (1).
AD = Alzheimer’s disease; AGD = argyrophillic grain disease; ApoE = apolipoprotein E; CDR = Clinical Dementia Rating; CVD = cerebrovascular disease; MCI = mild cognitive impairment; DLB = dementia with Lewy bodies; FTD = frontotemporal dementia; FTLD = frontotemporal lobar degeneration; MMSE = Mini-Mental State Examination; SIVD = subcortical ischaemic vascular disease; TPD = tangle-predominant dementia.