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. 2020 Jan 14;12:14. doi: 10.1186/s13195-019-0572-2

Table 1.

Subject demographics, neuropsychological, and clinical data

Control (n = 102) PMC (n = 40) SMC (n = 30) P value PMC vs. Control P value SMC vs. PMC
Age (years) 44.4 (12.6) 36.3 (15.7) 50.5 (9.4) 0.002** < 0.001***
Sex (male/female) 37/65 14/26 18/12 0.887 0.038#
Education (years) 11.0 (5.3) 12.1 (4.1) 10.5 (4.2) 0.249 0.118
EYO (years) N/A −11.6 (13.2) 4.1 (3.1) < 0.001***
MMSE 29.0 (1.6) 28.8 (1.8) 16.5 (8.0) 0.498 < 0.001***
MoCA 27.1 (2.3) 27.1 (3.0) 12.7 (7.7) 0.872 < 0.001***
CDR N/A N/A 1.3 (0.8)
Subject numbers
APP/PS1/PS2 N/A 17/21/2 9/18/3 0.474
APOEε4 (Y/N) 26/76 8/32 10/20 0.490 0.207
 T1 MRI after PP 95 40 28
 DTI after QC+PP 45 24 9
 rsfMRI after QC+PP 84 30 19

For continuous variables, data are shown in mean (SD), and the independent sample t-test was used for group comparison; for categorical variables, the chi-square test was used for group comparison. Bonferroni correction was used to correct for multiple comparison. #0.025 < P < 0.05, **0.001 < P < 0.01, ***P < 0.001

Y/N the number of subjects carrying (Y) or not carrying (N) APOEε4, PP preprocessing, QC quality control, PMC presymptomatic mutation carriers, SMC symptomatic mutation carriers, EYO estimated years from symptom onset, MMSE Mini-Mental State Examination, MoCA Montreal Cognitive Assessment, CDR Clinical Dementia Rating scale