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. 2022 May 13;145(10):3546–3557. doi: 10.1093/brain/awac175

Table 3.

Association between plasma p-tau181, Alzheimer’s disease neuropathology and regional p-tau severity

OR 95% CI P-value AUC (95% CI), P-value
Autopsy-confirmed Alzheimer’s disease (n = 62 versus n = 41 non-Alzheimer’s disease)
 Model 1 1.05 1.02–1.09 <0.01 0.73 (0.63–0.83), <0.01
 Model 2 1.06 1.02–1.10 <0.01 0.76 (0.67–0.86), <0.01
 Model 3 1.07 1.03–1.11 <0.01 0.82 (0.74–0.91), <0.01
Autopsy-confirmed Alzheimer’s disease, CDR <1.0 (n = 25 Alzheimer’s disease versus n = 32 non-Alzheimer’s disease)
 Model 1 1.04 0.99–1.08 0.05 0.71 (0.57–0.84), <0.01
 Model 2 1.05 1.01–1.10 0.02 0.78 (0.65–0.91), <0.01
Autopsy-confirmed Alzheimer’s disease, CDR ≥1.0 (n = 37 Alzheimer’s disease versus n = 9 non-Alzheimer’s disease)
 Model 1 1.23 1.05–1.45 0.01 0.85 (0.73–0.97), <0.01
 Model 2 1.25 1.02–1.53 0.03 0.89 (0.78–0.99), <0.01
Braak stage (n = 103) 1.06 1.02–1.09 <0.01
CERAD neuritic plaque score (n = 103) 1.05 1.02–1.08 <0.01
Regional p-tau severity (n = 90)
 Superior temporal cortex 1.06 1.02–1.09 <0.01
 Inferior parietal cortex 1.04 1.01–1.07 <0.01
 Entorhinal cortex 1.06 1.02–1.10 <0.01
 Amygdala 1.04 1.01–1.07 0.03
 CA1-hippocampus 1.06 1.02–1.10 <0.01
 CA2-hippocampus 1.03 1.01–1.06 0.02

Binary logistic regression examined the association between plasma p-tau181 levels and Alzheimer’s disease neuropathologic changes (per NIA–Reagan criteria). Model 1 examined plasma p-tau181 alone. Model 2 controlled for age at death, years between last blood draw and death, sex and APOE ε4 status. Model 3 controlled for Model 2 covariates in addition to global CDR (<1 and 1 or higher) score at time of blood draw. The AUC statistics for Models 2 and 3 were calculated using predicted probabilities from the binary logistic regression. P-values that examined the semiquantitative ratings of regional p-tau severity as outcomes (six total outcomes) were false discovery rate-adjusted using the Benjamini–Hochberg procedure and covariates included age at death, years between last blood draw and death, sex and APOE ε4 status.