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Table 1 Age, gender distribution of the 3 patient cohorts and the respective distribution of Aβ phases, Aβ-MTL phases, A-scores, Braak NFT-stage, CERAD neuritic plaque score, NIA-AA degree of AD pathology, diagnosis, PET-Aβ phase estimate, B-Aβ stage, B-Aβ plaque stage, Aβ load. Short description of the recruitment criteria of the cohorts and case selection criteria for this study

From: Different aspects of Alzheimer’s disease-related amyloid β-peptide pathology and their relationship to amyloid positron emission tomography imaging and dementia

 

Cohort 1

Cohort 2

Cohort 3

German cases

Leuven cases

[18F]flutemetamol phase 3 autopsy cases

Number of cases

95

79

97

Age in years (mean/range)

72,43 (35–98)

67,43 (34–90)

80,86 (59–95)

male/female

48/47

54/25

45/52

Aβ phase (mean/range)

2,34 (0–5)

1,8 (0–5)

3,65 (0–5)

AβMTL phase (mean/range)

1,96 (0–4)

1,47 (0–5)

2,92 (0–4)

A-score (mean/range)

1,49 (0–3)

1,18 (0–3)

2,39 (0–3)

Braak NFT-stage (mean/range)

2,11 (0–6)

2,27 (0–6)

3,95 (0–6)

CERAD neuritic plaque score (mean/range)

0,53 (0–3)

0,66 (0–3)

1,86 (0–3)

NIA-AA degree of AD pathology (mean/range)

1,11 (0–3)

0,97 (0–3)

2,01 (0–3)

Diagnosis (control/p-preAD/AD/AD+non-AD-D*/non-AD-D*)

24/35/13/5/18

18/4/15/8/34

3/8/33/28/25

PET-Aβ phase estimate (mean/range)

n.a.

n.a.

1,81 (0–3)

Aβ load / % (mean/range)

4,16 (0–23,34)

n.a.

6,75 (0–17,63)

B-Aβ stage (mean/range)

1,42 (0–3) [n = 38]

n.a.

n.a.

B-Aβ plaque stage (mean/range)

1,74 (0–3) [n = 70]

n.a.

n.a.

CAA severity grade (Vonsattel)

1 (0–3)

0,84 (0–3)

1,51 (0–3)

CAA stage of topographical distribution

1,1 (0–3)

0,72 (0–3)

1,64 (0–3)

CDR

0,993 (0–3) [n = 88]

1622 (0–3) [n = 74]

n.a.

MMSE

n.a.

n.a.

9,48 (0–30) [n = 65]

Scan-death interval

n.a.

n.a.

215 (0–846) days

Recruitment strategy

Hospital-based autopsies

Memory clinic-based cohort

Terminally ill with life-expectancy of less than 3 years, ≥55 years of age, no pregnancy, no allergy against [18F]flutemetamol, physical status allows to undergo PET imaging

Case selection criteria

Aβ phases, AβMTL phases and Aβ loads already determined in the context of previous studies

Aβ phases and AβMTL phases already determined for biobank purposes

[18F]flutemetamol amyloid PET images are available that allow the measurement of SUVRcort and SUVRcaud

  1. *Non-AD dementia (non-AD-D) includes cases with Lewy body disease, frontotemporal lobar degeneration with TDP43 (FTLD-TDP), fused in sarcoma (FTLD-FUS), or τ pathology (FTLD-tau: progressive supranuclear palsy, corticobasal degeneration, argyrophilic grain disease, Pick’s disease, and neurofibrillary tangle predominant dementia), encephalitis, Creutzfeldt-Jacob disease, tumor, vascular dementia and metabolic encephalopathy. These non-AD-D cases served as non-AD control cases from diseased brains to determine the differential diagnostic properties of the respective parameters