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. Author manuscript; available in PMC: 2018 Nov 6.
Published in final edited form as: Alzheimers Dement. 2018 May 21;14(10):1281–1292. doi: 10.1016/j.jalz.2018.04.011

Table 1.

Characteristics of the participants

Harvard aging brain study
Alzheimer’s disease neuroimaging initiative
Clinical diagnoses CN (n = 279) MCI (n = 51) AD (n = 16) CN (n = 367) MCI (n = 523) AD (n = 197)
Age, y 73.7 (6.1) 72.8 (8.8) 68.1 (9.7) 74.7 (6.6) 72.7 (7.9) 75.3 (7.8)
Education, y 15.8 (3.0) 16.5 (3.1) 15.5 (2.3) 16.5 (2.6) 16.1 (2.7)* 15.9 (2.7)*
Female, % 59.5% 35.3%* 31.3%* 53.1% 43.2%* 41.6%*
E4 carriers, % 29.0%, missing = 3 40.6%, missing = 19 75.0%, missing = 12 27.8%, missing = 0 46.7%, missing = 0 64.5%, missing = 0
Baseline MMSE 29.0 (1.0) 27.6 (1.4) 20.1 (4.1) 29.0 (1.2) 28.0 (1.7) 22.8 (3.1)
PET-Aβ stages, 0/1/2; N and % 192/44/40; 70/16/14% 23/6/22; 45/12/43% 1/0/15; 6/0/94% 228/110/28; 62/30/8% 209/152/162; 40/29/31% 24/38/134 12/19/68%
Serial PET interval, y 3.4 (1.3), missing = 135 2.3 (0.9), missing = 47 3.2 (1.5), missing = 14 2.4 (0.8), missing = 99 2.6 (0.9),* missing = 161 2.2 (0.6), missing = 146
Cognitive follow-up, y 3.6 (1.3) 2.7 (2.2) N/A 3.1 (1.4) 3.3 (1.4)* N/A

Abbreviations: Aβ, amyloid β; AD, Alzheimer’s dementia; CN, clinically normal participants; MCI, mild cognitive impairment.

NOTE. * and represent values significantly different from CN of the corresponding cohort.

*

P < .050

P < .001

NOTE. Statistics: two-sample t-tests except for sex, genotype, and PET-Aβ stages for which χ2 are used.

NOTE. Age and MMSE are given at the closest time of baseline PET.

NOTE. N/A represents that cognitive follow-up data were not analyzed in participants who had AD dementia at baseline.