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. 2024 Jan 6;147(1):12. doi: 10.1007/s00401-023-02659-w

Table 1.

Demographics of the Paris and TRIAD CSF cohorts

Paris cohort (n = 212) CU−
(n = 21)
MCI−
(n = 39)
NonAD−
(n = 25)
MCI+ 
(n = 48)
NonAD+ 
(n = 6)
AD
(n = 73)
P value
Age 64.38 (9.50) 66.87 (9.87) 65.96 (8.04) 71.85 (7.74) 67.33 (7.09) 71.97 (8.43)  < 0.001
Males (%) 14 (66.7) 24 (61.5) 11 (0.44) 31 (64.6) 3 (50) 46 (63.0) ns
APOE ε4 carriers (%) 6/21 (28.6) 5/24 (20.8) 5/6 (83.3) 27/48 (56.3) 4/39 (10.3) 47/72 (65.3)  < 0.001
MMSE score (available cases) 20 37 25 47 6 72
MMSE score 27.15 (2.52) 24.22 (3.87) 24.12 (4.95) 23.62 (4.54) 18.33 (6.62) 19.08 (5.63)  < 0.001
Lumipulse CSF (pg/mL)
 Aβ42/40 0.09 (0.01) 0.09 (0.01) 0.09 (0.01) 0.05 (0.01) 0.06 (0.005) 0.042 (0.01)  < 0.001
 p-tau181 32.81 (8.64) 36.73 (15.15) 32.74 (10.26) 86.22 (47.55) 51.93 (16.90) 115.62 (59.85)  < 0.001
 t-tau 243.10 (70.88) 301.28 (140.85) 364.24 (355.66) 565.52 (279.29) 365.17 (133.30) 736.05 (394.52)  < 0.001
GU CSF biomarkers (pg/mL)
 p-tau202 1.93 (0.96) 2.41 (1.45) 2.09 (1.53) 3.07 (1.64) 2.34 (2.52) 3.66 (1.67)  < 0.001
 p-tau205 1.56 (0.30) 1.94 (1.41) 1.59 (0.60) 3.83 (1.86) 2.72 (1.13) 5.33 (2.69)  < 0.001
TRIAD cohort (n = 262) Young
(n = 27)
CU−
(n = 74)
MCI−
(n = 17)
NonAD−
(n = 28)
CU+ 
(n = 33)
MCI+ 
(n = 35)
NonAD+ 
(n = 5)
AD
(n = 43)
P value
Age, years 23.0 (1.9) 68.8 (9.8) 68.2 (11.6) 62.2 (11.4) 70.4 (7.0) 71.3 (6.0) 71.0 (6.2) 65.2 (8.0)  < 0.001
Males (%) 11 (40.7) 30 (40.5) 9 (52.9) 11 (39.3) 13 (39.4) 15 (42.9) 2 (40.0) 21 (48.8) ns
Formal education, years 16.7 (1.5) 15.6 (4.3) 12.6 (5.9) 12.3 (6.0) 14.2 (3.4) 15.5 (4.2) 5.8 (8.3) 12.3 (6.2)  < 0.001
APOE ε4 carriers (%) 6/27 (22.2) 17/74 (23.0) 2/15 (13.3) 3/21 (14.3) 13/33 (39.4) 20/32 (62.5) 2/4 (50.0) 22/35 (62.9)  < 0.001
MMSE score (available cases) 27 69 14 15 31 29 2 31
MMSE score 29.78(0.51) 29.20(1.02) 28.14(1.56) 25.60(5.99) 29.13(0.88) 28.10(1.99) 24.50(2.12) 20.64(6.13)  < 0.001
Lumipulse CSF (pg/mL)
 Aβ42/40 0.09 (0.01) 0.09 (0.01) 0.09 (0.01) 0.09 (0.01) 0.05 (0.01) 0.05 (0.01) 0.05 (0.01) 0.04 (0.01)  < 0.001
 p-tau181 22.5 (7.1) 33.9 (10.8) 40.2 (12.0) 31.2 (12.7) 58.3 (32.4) 79.5 (38.0) 64.4 (22.6) 126.7 (79.5)  < 0.001
 t-tau 195.4 (47.6) 292.7 (112.7) 320.4 (89.0) 307.4 (156.2) 419.9 (184.9) 504.8 (208.7) 620.0 (398.5) 839.8 (456.2)  < 0.001
 Aβ-PET (available cases) 27 67 14 20 32 34 1 32
 SUVR 1.21 (0.07) 1.29 (0.12) 1.37 (0.16) 1.26 (0.22) 1.83 (0.48) 2.33 (0.55) - 2.30 (0.51)  < 0.001
 Tau-PET (available cases) 26 67 14 19 31 33 1 32
 SUVR 0.84(0.08) 0.83 (0.09) 0.81(0.09) 0.82(0.11) 0.95(0.23) 1.33(0.55) - 2.37 (0.89)  < 0.001
 VBM (available cases) 26 64 14 18 30 30 1 30
mm3 0.57(0.06) 0.46(0.05) 0.44(0.04) 0.41(0.07) 0.46(0.05) 0.43(0.06) - 0.39(0.07)  < 0.001
GU CSF biomarkers (pg/mL)
 p-tau202 1.05 (0.72) 1.81 (1.03) 1.42 (0.65) 2.10 (1.38) 2.21 (1.16) 2.57 (1.24) 2.83 (0.85) 3.26 (1.52)  < 0.001
 p-tau205 1.19 (0.37) 1.75 (0.48) 1.90 (0.39) 1.62 (0.53) 2.72 (1.37) 3.85 (1.59) 3.25 (0.72) 5.50 (2.87)  < 0.001

Data are shown as mean (SD) or n (%), as appropriate. Kruskal Wallis test was used to compare age between groups and Pearson’s chi-square to compare sex and APOE ε4 frequencies between groups. Years of education, MMSE and biomarkers levels were compared with a one-way ANOVA adjusted by age and sex

Abbreviations: Aβ42/40 ratio β-amyloid 42 and 40, AD Alzheimer’s disease, CSF cerebrospinal fluid, CU cognitively unimpaired, GU Gothenburg University Simoa assay, MCI mild cognitive impairment, MMSE Mini-Mental State Examination, NonAD non-Alzheimer’s disease, ns non-significant, p-tau181 tau phosphorylated at threonine 181, p-tau202 tau phosphorylated at serine 202, p-tau205 tau phosphorylated at threonine 205, PET positron emission tomography, SUVR standardized uptake value ratio, t-tau total tau, VBM voxel-based morphometry.