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. Author manuscript; available in PMC: 2024 Feb 1.
Published in final edited form as: Alzheimers Dement. 2022 Jun 4;19(2):602–610. doi: 10.1002/alz.12699

TABLE 3.

Associations between APOE allele and cognitive function

Caribbean
Hispanicsc
N = 5947
Hispanic
Americansd
N = 576
Blacks/African
Americansd
N = 917
Non-Hispanic
White
Americansd
N = 6070
Panel A: Dementia status a
Any ε4 1.92 [1.62–2.22] 1.64 [0.81–2.47] 1.26 [0.81–1.71] 1.83 [1.26–2.40]
Any ε2 0.87 [0.65–1.09] 0.82 [0.07–1.56] 1.26 [0.78–1.74] 1.01 [0.60–1.42]
Panel B: Immediate recall b
Any ε4 0.94 [0.92–0.96] 0.95 [0.88–1.03] 0.96 [0.92–1.01] 0.95 [0.93–0.96]
Any ε2 1.00 [0.98–1.03] 1.04 [0.94–1.16] 0.98 [0.93–1.03] 1.00 [0.98–1.02]
Panel C: Delayed recall b
Any ε4 0.90 [0.87–0.93] 0.91 [0.81–1.03] 0.84 [0.76–0.93] 0.91 [0.88–0.93]
Any ε2 1.00 [0.96–1.04] 1.10 [0.96–1.25] 0.98 [0.88–1.09] 1.01 [0.98–1.05]
a

Coefficients reported in Panel A are prevalence ratios (PRs) estimated from logistic regressions with dementia status as the dependent variable. PRs are interpreted as the ratios of estimated dementia prevalence between those with a particular APOE allele (e.g., ε4) to those without the allele in each sample. Ninety-five percent confidence intervals of the PRs are in brackets. All regressions adjusted for age, age squared, sex, and education.

b

Coefficients reported in Panels B and C are incidence rate ratios (IRRs) estimated from Poisson regressions with number of correct words recalled in 10-word immediate recall (Panel B) and 10-word delayed recall (Panel C) as the dependent variable. IRRs are interpreted as the ratios of expected number of words recalled between those with a particular APOE allele to those without the allele in each sample. Ninety-five percent confidence intervals of the IRRs are in brackets. All regressions adjusted for age, age squared, sex, and education.

c

Country indicators were additionally adjusted for the Caribbean Hispanics sample.

d

Prevalence ratios, incidence rate ratios, and their confidence intervals for US samples are from weighted regressions using person-level analytic weights. Number of observations for each sample is unweighted.

Abbreviation: APOE, apolipoprotein E.