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. 2020 Sep;130:100–110. doi: 10.1016/j.cortex.2020.05.016

Table 1.

Summary of demographic, clinical and phobic reactivity data for participant groups.

Characteristic Controls bvFTD svPPA nfvPPA AD
General clinical
No. (female: male) 25:30 13:33 9:11 12:13 15:14
Age, years 64.9 (7.3) 64.5 (6.3) 65.8 (7.1) 69.3 (7.7) 70.9 (7.8)b,c
Symptom duration, years NA 6.8 (4.7) 5.5 (2.3) 4.8 (4.5) 6.7 (3.4)
MMSE (/30) 29.4 (.9)a 24.2 (5.6)b 23.7 (6.0)b 20.8 (7.9)b,c 19.2 (6.0)b,c
General neuropsychiatric symptomsd
Apathy, n (%) 2 (4.9)a 37 (88.1)b 9 (47.4)b,c 14 (60.9)b,c 20 (69.0)b
Hallucinations, n (%) 0 11 (26.2) 1 (5.3) 0 4 (13.8)
Delusions, n (%) 0 17 (40.5) 4 (21.1) 3 (13.0)c 4 (13.8)c
Anxiety, n (%) 3 (7.3)a 19 (45.2)b 11 (57.9)b 17 (73.9)b,c 16 (55.2)b
Agitation, n (%) 0 16 (38.1) 4 (21.1) 3 (13.0)c 2 (6.9)c
Altered self-boundaries, n (%) 0 9 (37.5) 5 (26.3) 3 (15) 3 (10.3)c
Phobic reactivity
Altered phobic reactions (any), n (%): 2 (3.6) 8 (17.4) 3 (15) 3 (12) 1 (3.5)
OR (95% CI) versus healthy controlse NA 5.6 (1.1–28.2)b 4.6 (.7–30.0) 3.1 (.5–20.4) .8 (.1–9.2)
Acquired new phobia, n (%) 0 4 (8.7) 2 (10) 2 (8) 0
Loss of previous phobia, n (%) 2 (3.6) 4 (8.7) 1 (5) 1 (4) 1 (3.5)

Mean (SD) values are shown unless otherwise indicated. Key: asignificantly different from disease groups, p < .05; bsignificantly different from healthy control group, p < .05; csignificantly different from bvFTD group, p < .05; dof any severity (see text and Table S1); elogistic regression adjusted for age and gender; AD, patient group with typical Alzheimer's disease; bvFTD, patient group with behavioural variant frontotemporal dementia; CI, 95% confidence interval; Controls, healthy control group; MMSE, Mini-Mental State Examination score; NA, not applicable; nfvPPA, patient group with non-fluent variant primary progressive aphasia; OR, odds ratio; SD, standard deviation; svPPA, patient group with semantic variant primary progressive aphasia.