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. 2018 Jan 9;9:437. doi: 10.3389/fnagi.2017.00437

Table 2.

Sample demographic and clinical characteristics.

Variable Total sample Cognitively healthy at follow-up EarlyMCI at follow-up p-value
n 264 200 64
eMCI cognitive status at first speech sample 20 28
Age at first speech sample 61.8 (6.5) 61.1 (6.5) 64.2 (5.9) 0.04
Age at second speech sample 64.2 (6.6) 63.6 (6.7) 66.3 (5.9) 0.04
Sex (n; %F) 180; 67.4% 141; 70% 36; 56% 0.03
Education (y) 16.4 (2.8) 16.5 (2.7) 16.0 (2.8) 0.13
WRAT-III standard score 106.7 (9.3) 106.7 (8.9) 106.7 (10.3) 0.52
APOE ε4 allele (n; %ε4 +) 104; 39% 80; 40% 22; 34% 0.49
Parental history of AD (n; %+) 213; 79.8% 159; 80% 52; 81% 0.83
Ethnicity (n; % white) 252; 95.8% 194; 97% 58; 91%
CES-D 6.6 (0.49) 5.2 (0.77) 0.83
Self-reported hearing loss (n; %+) 9; 3% 7; 4% 2; 3% 0.80

eMCI, early Mild Cognitive Impairment; F/M, female/male; WRAT-III, Wide Range Achievement Test – Third Edition, reading subtest; APOE, apolipoprotein E; AD, Alzheimer’s disease; CES-D, Clinical Evaluation Scale of Depression, MMSE, Mini-Mental State Examination; RAVLT, Rey Auditory Verbal Learning Test, Total score. Items in bold indicate statistically significant difference between CH and eMCI at p < 0.05.