Table 1

Demographics, clinical, pathological and CSF data

FTLD-TauFTLD-TDPADControlP values*
n24259777
Age at CSF collection (years)66.9 (11.3)66.4 (8.7)71 (10.6)68.2 (9)0.06
Female, n (%)6 (25)13 (52)45 (46)50 (65)0.004
Education (years)15.6 (3.5)15.1 (2.7)14.8 (3.1)16.2 (3.2)0.05
Age at death (years)71.4 (12.6)70 (9.5)76.6 (10.6)NA0.008
Participants with no AD pathology (NIA-AA stage ≤B1), n (%)20 (83)18 (72)0NA0.003
Time interval, onset–CSF (years)3.8 (2.7)3.7 (2.7)4.3 (2.6)NA0.521
Time interval, CSF–death (years)4.5 (3.6)3.6 (3)5.6 (3.6)NA0.029
Total disease duration, onset–death (years)8.5 (4.6)7.2 (3.3)9.8 (4.1)NA0.013
sAPPβ (ng/mL)477.5 (120)544.9 (239.4)717.1 (441.6)848.4 (381.9)<0.001
YKL-40 (ng/mL)299.8 (69.1)265.6 (48.5)268.2 (77.2)210.3 (55.1)<0.001
sAPPβ:YKL-40 ratio1.67 (0.56)2.07 (0.78)2.77 (1.5)4.19 (1.89)<0.001
  • Unless otherwise specified, results are expressed as mean (SD).

  • *P values were obtained by comparing the groups of FTLD-Tau, FTLD-TDP, AD and control. Tukey’s honest significant differences post-hoc comparisons are detailed in figure 2.

  • AD, Alzheimer’s disease; CSF, cerebrospinal fluid; FTLD, frontotemporal lobar degeneration; NA, not applicable; NIA-AA, National Institute on Aging-Alzheimer’s Association; sAPPβ, soluble β fragment of amyloid precursor protein.