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Table 1 Demographics of the cohort

From: Clinical outcomes up to 9 years after [18F]flutemetamol amyloid-PET in a symptomatic memory clinic population

 

Complete dataset

Subset with longitudinal clinical and cognition data

 

Total

(N = 200)

VR − 

(N = 72)

VR + 

(N = 128)

Total

(N = 108)

VR − 

(N = 35)

VR + 

(N = 73)

Age

61.75 ± 5.8

61.63 ± 5.5

61.82 ± 6.0

61.6 ± 5.9

62.3 ± 5.4

61.2 ± 6.1

Sex (F)

91 (45.5%)

23 (31.9%)

68 (53.1%)

48 (44.4%)

11 (31.4%)

37 (50.7%)

APOE-ε4 carriership

111 (55.5%)

25 (34.7%)

86 (67.2%)

89 (60.2%)

13 (39.4%)

52 (76.5%)

Clinical diagnosis (post-PET)

 SCD

4 (2.0%)

4 (5.6%)

n/a

n/a

n/a

n/a

 MCI

12 (6.0%)

11 (15.3%)

1 (0.8%)

8 (7.4%)

7 (20.0%)

1 (1.4%)

 Dementia

184 (92.0%)

57 (79.2%)

127 (99.2%)

100 (92.6%)

28 (80.0%)

72 (98.6%)

Etiological diagnosis (post-PET)

 AD

124 (62.0%)

2 (2.8%)

122 (95.3%)

71 (65.7%)

1 (2.9%)

70 (95.9%)

 Vascular

3 (1.5%)

3 (4.2%)

n/a

2 (1.9%)

2 (5.7%)

n/a

 FTLD

30 (15.0%)

29 (40.3%)

1 (0.8%)

13 (12.0%)

13 (37.1%)

n/a

 DLB

11 (5.5%)

7 (9.7%)

4 (3.1%)

7 (6.5%)

4 (11.4%)

3 (4.1%)

 ND other

9 (4.5%)

8 (11.1%)

1 (0.8%)

4 (3.7%)

4 (11.4%)

n/a

 Non-ND

23 (11.5%)

23 (31.9%)

n/a

11 (10.2%)

11 (31.4%)

n/a

  1. SCD subjective cognitive decline, MCI mild cognitive impairment, AD Alzheimer’s disease, FTLD frontotemporal lobar degeneration, DLB Lewy body disease, ND neurodegeneration, VR visual read