Skip to main content
. Author manuscript; available in PMC: 2020 Dec 31.
Published in final edited form as: J Alzheimers Dis. 2020;78(1):467–477. doi: 10.3233/JAD-200228

Table 3.

APOE haplotypes effects on neuropathological features measured in autopsies of AD cases and non-AD controls. Odds ratios and p-values are obtained from a logistic or ordinal regression model controlling for confounders and the dosages of the different haplotypes. ε3 is taken as the reference haplotype

AD Control
E2 E4 Anc. E4 Eur. E2 E4 Anc. E4 Eur.
Whole brain weight 0.96 0.91 1.04 1.04 0.74 0.64*
Fresh or fixed weight 1.3 1 1 0.69 0.57 0.26
Cerebral cortex atrophy 1.07 1.11 1.01 0.8 1.16 1.91**
Lobar atrophy 0.73 0.66 1.03 1 12* 1.1
Hippocampus atrophy 1.08 1.17 1.03 1.11 0.99 0.69
White matter rarefaction 0.9 1.11 1.03 0.79 1.34 0.93
Arteriolosclerosis 0.78 0.85 0.97 1.12 1.61 1.91
Atherosclerosis 0.99 1.06 0.93 0.8 1.03 0.81
Microinfarcts 1.52 1.57 1.16 0.58 0.68 0.44
Infarcts 0.56 1.3 1.3 1.1 1.40E–07 0.55
Braak stage for neurofibrillary degeneration 0.78* 1.23* 1.3**** 1.33 2.79*** 1.19
CERAD score for neuritic plaques 0.74** 1.3** 1.34**** 0.73 1.35 1.26
NIA-AA ADNC 0.73 1.17 1.28*** 0.81 2.33 1.77*
*

p < 0.05,

**

p < 0.01,

***

p < 0.001,

****

p < 0.0001.