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. 2018 Feb;62:191–196. doi: 10.1016/j.neurobiolaging.2017.10.008

Table 1.

Demographics of participants included in the analysis

Variable Noncarriers C9orf72
GRN
MAPT
p-value
Presymptomatic Affected Presymptomatic Affected Presymptomatic Affected All groups At-risk groups (including noncarriers) Affected groups
N 144 40 25 65 12 23 10 - - -
Age, mean (SD) 48.7 (14.3) 43.5 (10.5) 65.2 (7.7) 48.9 (10.7) 63.2 (6.0) 38.6 (9.0) 57.2 (5.9) <0.001 <0.001 0.011
%Female 63 63 28 63 67 61 30 0.021 1.000 0.083
EYO, mean (SD) −10.5 (14.2) −15.0 (12.5) 5.8 (5.0) −10.3 (11.3) 1.4 (2.1) −11.8 (10.3) 5.9 (3.5) <0.001 0.270 0.001
Education, y 13.8 (3.4) 13.9 (3.0) 13.1 (4.5) 14.1 (3.1) 10 (3.8) 13.4 (3.4) 12.2 (4.7) 0.040 0.788 0.125
Disease duration, y N/A N/A 6.6 (4.8) N/A 2.5 (1.3) N/A 4.9 (5.3) N/A N/A 0.010
MMSE (max = 30) 29.2 (1.3) 29.2 (1.2) 24.8 (4.2) 29.1 (1.4) 20.7 (6.2) 29.4 (1.4) 24.7 (4.9) <0.001 0.359 0.139

Diagnoses in affected subjects: bvFTD 33 (18 C9orf72, 5 GRN, 10 MAPT), 3 FTD-ALS (all C9orf72), 7 nonfluent variant primary progressive aphasia (PPA) (2 C9orf72, 5, GRN), 1 semantic variant PPA (C9orf72), 1 corticobasal syndrome (GRN), 1 dementia - not otherwise specified (C9orf72).

Bold text indicates a statistically significant difference (p< 0.05) between groups.