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. Author manuscript; available in PMC: 2020 Jul 1.
Published in final edited form as: Alzheimers Dement. 2019 Jun 1;15(7):888–898. doi: 10.1016/j.jalz.2019.04.001

Table 1.

Baseline characteristics according to diagnosis

Preclinical AD
(n = 438)
Prodromal AD
(n = 729)
Mild AD dementia
(n = 1867)
Moderate to
severe AD
dementia
(n = 234)
p-value overall
group difference
Age (years) 73 (7) 72 (7) 73 (9) 75 (10) <0.01a
Male (n) 204 (47%) 417 (57%) 781 (42%) 74 (33%) <0.01
MMSE (0-30, median (IQR)) (n=3252) 29 (28-30) 27 (26-29) 22 (19-24) 16 (13,19) <0.01b
APOE ε4 genotype* (n) (n=1984) 210 (49%) 466 (66%) 554 (71%) 35 (51%) <0.01
Abnormal CSF total tau* (n) (n=1563) 87 (38%) 346 (57%) 535 (80%) 47 (82%) <0.01
Follow-up years (median (IQR)) 3.8 (2-4.5) 3.9 (2.5-4.8) 2.0 (1.5-2.5) 2.0 (1.2-2.3) <0.01c
Progression to next clinical disease stage (n) 87 (20%) 325 (45%) 569 (30%) NA NA
Death at follow-up (n) 12 (3%) 76 (10%) 215 (12%) 54 (23%) NA
Participants by cohort (n ADC /ADNI /AIBL /DESCRIPA /Gothenburg /ICTUS) 40/180/191 /23 /4 /0 140 /449 /73 /49/18 / 0 507 /224 /69 /0/1 / 1066 64 /1/3 /0/0 / 166 NA

Mean (SD), unless otherwise specified. In Tukey posthoc:

a

Moderate to severe AD dementia older than the MCI and Mild AD dementia group;

b

All groups significantly different from each other;

c

Normal cognition and MCI longer follow-up than dementia groups

*

Available in subset of cohorts, APOE not for ICTUS