Skip to main content
. 2023 Sep 28;15(4):e12482. doi: 10.1002/dad2.12482

TABLE 4.

Cruchaga et al., 10  polygenic risk score in participants homozygous for APOE ε3; demographics, age of onset, APOE, and polygenic risk score across diagnostic groups.

Diagnostic group

(all APOE ε3/ε3 homozygotes)

Age of symptom onset (years) Age at first visit (years) Sex, % female Cruchaga et al., 10  PRS PRS odds ratio (95% CI) predicting diagnostic group versus controls PRS odds ratio (95% CI) predicting diagnostic group versus late‐onset AD

Early‐onset AD

‐Entire group

N = 77

55 (5.4)

59 (5.5)

49%

0.0032 (0.0098)

2.6 (1.2–6.0)

1.5 (0.71–2.9)

‐Multidomain

N = 37

54 (5.0) 58 (4.8) 46% 0.0019 (0.0091) 2.9 (1.2–7.5) 1.7 (0.71–3.9)

‐Logopenic variant PPA

N = 23

56 (6.2) 61 (6.4) 48% 0.0075 (0.010) 3.7 (1.1–13) 1.6 (0.58–4.4)

‐Posterior cortical atrophy

N = 17

55 (5.2) 59 (5.1) 59% 0.00068 (0.0098) 1.7 (0.52–5.4) 1.0 (0.34–3.2)

Late‐onset AD

N = 53 a

77 (6.6) 80 (7.3) 58% 0.0027 (0.086) 1.7 (0.70–4.0) N/A

Controls

N = 43

N/A 69 (6.6) 70% −0.0013 (0.0097) N/A 0.59 (0.25–1.4)

Note. Unless otherwise noted, all values are mean ± (standard deviation). Logistic regression co‐varies for sex.

Abbreviations: AD, Alzheimer's disease; APOE, apolipoprotein E; CI, confidence interval; PHS, polygenic hazard score; PPA, primary progressive aphasia; PRS, Cruchaga et al. polygenic risk score.

a

One late‐onset AD participant from the prior PHS group was not available at the time of data analysis (e.g., N = 53 instead of 54).