Table 1.
Study parameter | Entire | Controls, | AD only, | CTE only, | AD + CTE, |
[Median (IQR) | cohort, | n = 9 | n = 7 | n = 15 | n = 10 |
or n (%)] | n = 41 | ||||
Age, y | 72 (65–81) | 63 (46–69) | 81 (69.5–82.5) | 69 (46.5–74.5) | 81.5 (77.5–83.8) |
Sex, Male | 39 (95.1) | 8 (88.9) | 7 (100) | 14 (93.3) | 10 (100) |
Braak Stage | |||||
0 | 10 (25.6) | 5 (55.6) | 0 (0) | 5 (38.5) | 0 (0) |
I-II | 4 (10.3) | 3 (33.3) | 0 (0) | 1 (7.7) | 0 (0) |
III-IV | 11 (28.2) | 1 (11.1) | 1 (14.3) | 6 (46.2) | 3 (30) |
V-VI | 14 (35.9) | 0 (0) | 6 (85.7) | 1 (7.7) | 7 (70) |
CERAD Score | |||||
0 | 20 (48.8) | 8 (88.9) | 0 (0) | 12 (80) | 0 (0) |
1 | 10 (24.4) | 1 (11.1) | 1 (14.3) | 3 (20) | 5 (50) |
2 | 7 (17.1) | 0 (0) | 4 (57.1) | 0 (0) | 3 (30) |
3 | 4 (9.8) | 0 (0) | 2 (28.6) | 0 (0) | 2 (20) |
Study parameter | Entire | No CTE, | Low stage | High stage CTE | |
[Median (IQR) | cohort, | n = 16 | CTE (Stage I | (Stage III or | |
or n (%)] | n = 41 | or II), n = 5 | IV), n = 20 | ||
Age, y | 72 (65–81) | 69 (58.8–75.8) | 32 (27–46) | 77.5 (69.8–83) | |
Sex, Male | 39 (95.1) | 15 (93.8) | 5 (100) | 19 (95) | |
Braak Stage | |||||
0 | 10 (25.6) | 5 (31.2) | 4 (80) | 1 (5.6) | |
I-II | 4 (10.3) | 3 (18.8) | 0 (0) | 1 (5.6) | |
III-IV | 11 (28.2) | 2 (12.5) | 0 (0) | 9 (50) | |
V-VI | 14 (35.9) | 6 (37.5) | 1 (20) | 7 (38.9) | |
CERAD Score | |||||
0 | 20 (48.8) | 8 (50) | 4 (80) | 8 (40) | |
1 | 10 (24.4) | 2 (12.5) | 0 (0) | 8 (40) | |
2 | 7 (17.1) | 4 (25) | 1 (20) | 2 (10) | |
3 | 4 (9.8) | 2 (12.5) | 0 (0) | 2 (10) |
IQR, Interquartile range; AD, Alzheimer’s disease; CTE, chronic traumatic encephalopathy.