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. Author manuscript; available in PMC: 2020 Jul 1.
Published in final edited form as: Neurobiol Dis. 2019 Feb 21;127:142–146. doi: 10.1016/j.nbd.2019.02.016

Table 1:

Cohort characteristics and distribution of APOE genotypes in study populations

Controls AD PD CBD LBD MSA PSP
N 591 571 348 41 525 223 202
Mean Age ± SD (years)a 71.7 ± 11.0 81.8 ± 10.1 78.2 ± 9.4 74.8 ± 9.3 77.5 ± 8.2 66.1 ± 10.8 78.1 ± 9.7
Age range (years)a (50, 105) (41, 103) (19, 107) (51, 96) (49, 99) (20, 90) (55, 102)
No. Male (%) 318 (53.8) 221 (38.7) 234 (67.2) 18 (43.9) 338 (64.4) 109 (48.9) 113 (55.9)
No. Female (%) 273 (46.2) 350 (61.3) 114 (32.8) 23 (56.1) 187 (35.6) 114 (51.1) 89 (44.1)
No. Pathologically-confirmed 218 (36.9) 571 (100) 348 (100) 41 (100) 525 (100) 223 (100) 202 (100)
No. Clinically-defined 373 (63.1)b N/A N/A N/A N/A N/A N/A

No. with ε2/ε2 (%) 5 (0.8) 0 (0) 0 (0) 0 (0) 2 (0.4) 0 (0) 3 (1.5)
No. with ε2/ε3 (%) 83 (14.0) 29 (5.1) 54 (15.5) 4 (9.8) 35 (6.7) 25 (11.2) 20 (9.9)
No. with ε2/ε4 (%) 14 (2.4) 11 (1.9) 6 (1.7) 1 (2.4) 14 (2.7) 6 (2.7) 5 (2.5)
No. with ε3/ε3 (%) 368 (62.3) 208 (36.4) 203 (58.3) 28 (68.3) 239 (45.5) 141 (63.2) 138 (68.3)
No. with ε3/ε4 (%) 104 (17.6) 252 (44.1) 82 (23.6) 6 (14.6) 187 (35.6) 48 (21.5) 33 (16.3)
No. with ε4/ε4 (%) 17 (2.9) 71 (12.4) 3 (0.9) 2 (4.9) 48 (9.1) 3 (1.3) 3 (1.5)
a

Age was defined as age at death for pathologically-confirmed samples and age at specimen collection for clinically-defined control samples. Age information was available for 590/591 controls, 568/571 AD samples, 342/348 PD samples, 41/41 CBD samples, 523/525 LBD samples, 101/223 MSA samples, and 202/202 PSP samples.

b

DNA from clinically defined control samples was extracted from blood as opposed to brain tissue from all other cohorts.

Abbreviations: AD, Alzheimer’s disease; PD, Parkinson’s disease; CBD, corticobasal degeneration; LBD, Lewy body dementia; MSA, multiple system atrophy; PSP, progressive supranuclear palsy; SD, standard deviation; N/A, not applicable.