Skip to main content
. 2022 Oct 20;81(12):975–987. doi: 10.1093/jnen/nlac093

TABLE 1.

Demographic and Clinical Characteristics Among Participants With ADNC Only Versus ADNC + LATE-NC

Characteristic All n = 1100 ADNC n = 735 ADNC and LATE-NC n = 365 p value
Age at death, mean (SD) 83.2 (8.8) 82.5 (8.9) 84.5 (8.5) <0.001
Months between last UDS visit and death, mean (SD) 12.5 (9.3) 12.3 (9.1) 13.1 (9.8) 0.195
Years of education, mean (SD) 15.9 (3.1) 15.8 (3.2) 16 (3.0) 0.206
Female, n (%) 537 (48.8) 346 (47.1) 191 (52.3) 0.101
Nonwhite race, n (%) 77 (7.0) 48 (6.5) 29 (8.0) 0.725
APOE ε4 carrier, n (%) 530 (48.2) 328 (44.6) 202 (55.3) 0.003
Cognitive status at last UDS visit, n (%) <0.001
 Normal cognition 126 (11.5) 112 (15.2) 14 (3.8)
 Impaired, not MCI 20 (1.8) 16 (2.2) 4 (1.1)
 MCI 111 (10.1) 94 (12.8) 17 (4.7)
 Dementia 843 (76.6) 513 (69.8) 330 (90.4)
Primary clinical diagnosis, n (%) <0.001
 Normal cognition 126 (11.5) 112 (15.2) 14 (3.8)
 Alzheimer disease 766 (69.6) 465 (63.3) 301 (82.5)
 Lewy body disease 72 (6.6) 56 (7.6) 16 (4.4)
 Frontotemporal disorders* 49 (4.5) 37 (5.0) 12 (3.3)
 Other 84 (7.6) 63 (8.6) 21 (5.8)
CDR sum of boxes, mean (SD) 10.3 (6.8) 9.3 (7.0) 12.4 (5.7) <0.001
CDR global score, n (%) <0.001
 None 124 (11.3) 110 (15) 14 (4.2)
 Questionable 166 (15.1) 133 (18.1) 31 (9.3)
 Mild 156 (14.2) 107 (14.6) 47 (14.1)
 Moderate 233 (21.2) 136 (18.5) 88 (26.4)
 Severe 421 (38.3) 249 (33.9) 154 (46.1)
*

Includes MSA, PSP, CBD, FTLD with motor neuron disease (e.g. ALS), and other FTLD.

Missing data: ADNC: Education (n=7), Race (n=2), APOE ε4 (n=72), Primary clinical diagnosis (n=2); ADNC + LATE: Education (n=3), Race (n=1), APOE ε4 (n=31), Primary clinical diagnosis (n=1).

Bold values indicate statistical significance at the p<0.05 level.