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. 2022 Sep 7;27(11):4800–4808. doi: 10.1038/s41380-022-01729-x

Table 4.

Association of AD neuropathological burden and functional cognitive scores with local European or non-European APOE4 + ancestries using corresponding ancestries of APOE4− individuals as references.

(A) EUR APOE4 + local ancestry (n = 31)a Model 1 (no AFR adjustment) Model 2 (with AFR adjustment)
Outcomes Pathology adjustments β (95% CI) p β (95% CI) p
BB NA 0.52 (0.01; 1.03) 0.048 0.51 (−0.002; 1.03) 0.051
CERAD NA 0.61 (0.28; 0.95) <0.001 0.61 (0.27; 0.95) <0.001
CDR-SOB NA 1.22 (−0.49; 2.93) 0.16 1.29 (−0.41; 2.99) 0.14
BB + CERAD 0.52 (−1.06; 2.10) 0.52 0.55 (−1.02; 2.13) 0.49
BB 0.92 (−0.66; 2.50) 0.25 0.97 (−0.61; 2.54) 0.23
CERAD 0.25 (−1.34; 1.83) 0.76 0.31 (−1.27; 1.89) 0.70
(B) Non-EUR APOE4 + local ancestry (n = 17)b Model 1 (no AFR adjustment) Model 2 (with AFR adjustment)
BB NA −0.21 (−1.08; 0.65) 0.62 −0.21 (−1.10; 0.67) 0.62
CERAD NA 0.01 (−0.52; 0.70) 0.76 0.09 (−0.51; 0.69) 0.76
CDR-SOB NA 0.39 (−2.78; 3,56) 0.80 0.39 (−2.82; 3.60) 0.81
BB + CERAD 1.53 (−1.60; 4.66) 0.33 1.53 (−1.66; 4.72) 0.33
BB 1.45 (−1.41; 4.32) 0.31 1.45 (−1.46; 4.37) 0.32
CERAD 0.59 (−2.50; 3.67) 0.70 0.59 (−2.54; 3.73) 0.70

Model 1: Linear regression model adjusted for age, sex, education, and AD neuropathology when indicated.

Model 2: Linear regression model adjusted for age, sex, education, AD neuropathology when indicated, and AFR.

OBS. Only individuals homozygous for APOE local ancestry were included.

AFR African ancestry (continuous 10% increments), BB Braak & Braak, CERAD Consortium to Establish a Registry for Alzheimer’s disease, NA not applicable.

aReference for (A): Individuals APOE4− (genotypes 22, 23, or 33) with local European ancestries (n = 138).

bReference for (B): Individuals APOE4− (genotypes 22, 23 or 33) with local non-European ancestries (n = 24).