Skip to main content
. 2017 Mar;51:104–112. doi: 10.1016/j.neurobiolaging.2016.11.017

Table 1.

Cohort 1: demographic data, clinical characteristics, and CSF levels of biomarkers

Sample characteristics Control (n = 65) sMCI (n = 61) MCI-AD (n = 35) AD (n = 75) DLB/PDD (n = 34) VaD (n = 28) FTD (n = 41)
Sex F/M 42/23 34/27 23/12 51/24 13/21 13/15 21/20
Age 75 (6) 69 (7)∗∗∗ 75 (8) 76 (7) 72 (6) 75 (8) 72 (6)
MMSE 28.7 (1.7) 28.2 (1.2) 26.4 (1.7)∗∗∗ 19.5 (3.3) ∗∗∗ 21.4 (5.1)∗∗∗ 21.5 (4.5)∗∗∗ 22.8 (6.1)∗∗∗
APOE 1or 2 ε4 alleles 34% 48% 80%∗∗∗ 65%∗∗∗ 55% 21% 28%a
BMI 25.9 (3.7) 25.1 (3.2) 24.3 (4.2) 23.7 (3.6) 25.6 (3.4) 26.5 (5.8) 25.4 (4.1)
Qalb 6.3 (2.9) 6.3 (2.5) 7.1 (3.3) 7.6 (3.4)∗∗ 8.4 (4.6) 8.7 (3.7)∗∗ 8.6 (5.5)∗∗
Diabetes, yes/no 4/61 3/58 1/34 9/66 2/32 7/21 0/32
ICAM-1, ng/mL 2.0 (0.7) 1.9 (0.7) 2.1 (0.7) 2.2 (0.7) 2.0 (0.8) 2.1 (0.7) 2.0 (1.0)
VCAM-1, ng/mL 5.4 (1.4) 4.9 (1.5) 5.4 (1.6) 5.7 (1.6) 5.3 (1.4) 5.5 (1.5) 4.9 (1.6)
VEGF, pg/mL 58.0 (19.1) 65.0 (32.0) 70.9 (21.8)∗∗ 73.2 (27.7)∗∗ 67.0 (29.0) 80.8 (33.5)∗∗ 74.6 (31.6)∗∗
sVEGFR-1, pg/mL 149.2 (55.0) 111.4 (39.7)∗∗∗ 128.9 (44.7) 130.3 (41.1)∗∗ 103.3 (37.4)∗∗∗ 100.3 (30.3)∗∗∗ 118.0 (38.7)∗∗
VEGF/sVEGFR-1 0.4 (0.2) 0.6 (0.3)∗∗∗ 0.6 (0.2)∗∗∗ 0.6 (0.2)∗∗∗ 0.7 (0.4)∗∗∗ 0.9 (0.4)∗∗∗ 0.7 (0.3)∗∗∗
Aβ42, pg/mL 675.2 (289.8) 478.9 (195.0)∗∗∗ 314.5 (78.9)∗∗∗ 259.7 (105.0)∗∗∗ 349.6 (172.7)∗∗∗ 407.4 (187.0)∗∗∗ 682.9 (290.5)
Aβ40, pg/mL 5241 (1487) 3786 (1360)∗∗∗ 4219 (1327)∗∗∗ 3899 (1376)∗∗∗ 3240 (1200)∗∗∗ 3218 (1345)∗∗∗ 4530 (1536)

Data are shown as mean (standard deviation) unless otherwise specified. Demographic factors and clinical characteristics were compared using 1-way analysis of variance and chi-square tests. CSF biomarkers and the Qalb were analyzed with univariate general linear models controlling for age and gender, compared with controls p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001.

Key: Aβ, amyloid β; AD, Alzheimer's disease; BMI, body mass index; CSF, cerebrospinal fluid; DLB/PDD, dementia with Lewy bodies or Parkinson's disease with dementia; F, female; FTD, frontotemporal dementia; ICAM-1, intercellular adhesion molecule 1; M, male; MCI-AD, MCI that progressed to AD; MMSE, Mini-Mental State Examination; Qalb, CSF/plasma albumin ratio; sMCI, stable mild cognitive impairment; sVEGFR-1, soluble VEGF receptor 1; VaD, vascular dementia; VCAM-1, vascular cell adhesion molecule 1; VEGF, vascular endothelial growth factor.

a

APOE data were only available from 18 FTD patients.