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. Author manuscript; available in PMC: 2019 May 28.
Published in final edited form as: J Alzheimers Dis. 2018;64(4):1307–1324. doi: 10.3233/JAD-180514

Table 4.

Predicted mean (95% CI)* tau pathology by APOE ε4 carrier status

Year of death, 1997–2011 Year of death, 2012–2017
Adjusted Mean
NFTs
Adjusted Mean
NFT density
Adjusted Mean
tau burden
Model 1
APOE ε4 positive 16.0 (6.5–39.3) 16.8 (9.8–18.6) 54.3 (30.2–97.6)
APOE ε4 negative 6.8 (5.1–9.1) 8.7 (6.8–11.3) 24.6 (18.7–32.3)
Model 2
APOE ε4 positive 19.4 (7.0–53.9) 12.0 (6.9–21.0) 44.8 (24.7–81.2)
APOE ε4 negative 6.6 (5.0–8.8) 8.9 (7.0–11.4) 24.7 (18.9–32.3)
*

Results are based on negative binomial regression. Bolded results are significantly different between APOE positive and negative at 0.05. Model 1 includes APOE, Model 2 includes both APOE and amyloid pathology. For NFTs, the amyloid measure was diffuse plaque counts; amyloid density was used for NFT density; and amyloid burden was used for tau burden. All models were adjusted for age at death and sex.