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. 2020 Aug 4;76(3):941–953. doi: 10.3233/JAD-191261

Table 1.

Demographic data and CSF-biomarker levels of the included subjects at risk for FAD. Demographic characteristics of the mutation carrier group and the non-carrier group at the time of baseline CSF sampling. Age, expected years to symptom onset, and levels of Aβ42, YKL-40, and neurogranin are presented as mean values ± standard deviation. *Levels of t-tau and p-tau are presented as median with range, due to lack of normal distribution of the data. One of the mutation carriers is an APOE e2/e4 heterozygote and is included in the table as both an ɛ2 and an ɛ4 carrier. N, number; NS, not significant

Mutation carriers Non-carriers p
(n = 14) (n = 17)
Age 43±10 46±12 NS
Expected years to symptom onset –12±10 –9±12 NS
Gender (Male/Female) 11/3 10/7 NS
APOEɛ4 carriers (n) 8 7 NS
APOEɛ2 carriers (n) 1 3 NS
Aβ42 (pg/mL) 221±138 626±277 p < 0.0001
t-tau* (pg/mL) 472 (169–937) 241 (122–537) p = 0.01
p-tau* (pg/mL) 58 (28–104) 36 (19–76) p = 0.06
YKL-40 (ng/mL) 98±33 91±38 NS
Neurogranin (pg/mL) 252±90 215±84 NS