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Table 1 Demographics and clinical characteristics

From: Plasma apolipoprotein E levels in longitudinally followed patients with mild cognitive impairment and Alzheimer’s disease

 

N (F/M)

APOE ε4 allele status (− / − , + / − , + / +)

Age (years)

MMSE score

CSF Aβ42 (pg/mL)

CSF Aβ40 (pg/mL)

CSF Aβ42/Aβ40

CSF t-tau (pg/mL)

CSF p-tau (pg/mL)

Whole cohort

125 (71/54)

45, 50, 30

65.0 (53.0–84.0)

28.0 (16.0–30.0)

602.6 (173.0–1674.1)

15,387.0 (3553.0–33,373.5)

0.045 (0.010–0.120)

395.5 (98.5–2325.3)

67.4 (15.9–168.8)

Controls

39 (26/13)

23, 16, 0

69.0 (57.0–84.0)

29.0 (28.0–30.0)

1010.7 (628.8–1674.1)

16,635.0 (11,152.0–33,373.5)

0.062 (0.020–0.100)

264.1 (137.5–558.1)

53.5 (32.8–102.0)

MCI-MCI

30 (14/16)

11, 8, 11

64.0 (53.0–79.0)

28.0** (25.0–30.0)

591.5*** (173.0–1268.8)

13,477.0* (3553.0–31,343.0)

0.048 (0.010–0.120)

319.8 (98.5–1057.0)

55.7 (15.9–131.0)

MCI-ADD

28 (17/11)

7, 10, 11

63.5*** (56.0–71.0)

27.0*** (23.0–29.0)

526.7*** (282.7–1059.8)

13,667.5 (8021.0–23,258.8)

0.037*** (0.010–0.090)

557.9*** (163.0–2325.3)

86.3*** (37.3–168.8)

ADD

28 (14/14)

4, 16, 8

64.0*** (54.0–78.0)

23.0*** (16.0–27.0)

481.6*** (211.6–1092.2)

15,387.0 (6708.0–29,090.0)

0.034*** (0.010–0.080)

611.8*** (176.5–1540.0)

90.2*** (27.9–156.9)

p-value

nsa

 < 0.001a

 < 0.001b

 < 0.001b

 < 0.001c

0.035c

 < 0.001b

 < 0.001c

 < 0.001c

  1. Results are represented as median (minimum–maximum)
  2. MCI-MCI patients with amnestic mild cognitive impairment that did not fulfil the ADD diagnostic criteria upon 24 months follow-up, MCI-ADD patients with amnestic mild cognitive impairment that fulfilled the AD diagnostic criteria after 24 months, ADD patients with Alzheimer’s disease with dementia at baseline, F Females, M Males, APOE Apolipoprotein E gene, MMSE Mini mental state examination, 42 Amyloid-β42 peptide, Αβ40 Amyloid-β40 peptide, t-tau Total tau, p-tau Tau phosphorylated at Threonine 181 residue, ns non-significant, a chi-square test, b, c multiple comparison of the diagnostic groups using Kruskal–Wallis (b) or ANOVA (c)
  3. *p ≤ 0.05, **p ≤ 0.01, and ***p ≤ 0.001 indicate comparison of the patient groups with the control group using Tukey HSD or Dunn’s test followed by Bonferroni correction for multiple comparisons (n = 6)