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. 2016 Feb 12;5(2):e002886. doi: 10.1161/JAHA.115.002886

Table 2.

Biochemical Measurements for Study Participants

Parameters CH (n=47) MCI (n=35) AD (n=26) P Value
Cholesterol efflux (ratio) 1.56 (0.73)a, b 0.94 (0.35) 1.02 (0.43) <0.001
CSF supernatant PC, ng/mL 9047 (6668, 11 802)a, b 7382 (6108, 8717) 6669 (5506, 8367) 0.016
CSF nanoparticle PC, ng/mL 19 (14, 23) 19 (14, 29) 18 (14,22) 0.80
CSF supernatant SM, ng/mL 2091 (718) 1837 (643) 1722 (561) 0.14
CSF nanoparticle SM, ng/mL 102 (50) 90 (35) 93 (41) 0.11
Plasma cholesterol, mg/dL 181 (31) 180 (39) 185 (33) 0.99
CSF cholesterol, μg/mL 3.49 (0.84) 3.21 (0.75) 3.16 (0.56) 0.04
ApoE levels, μg/mL 7.2 (2.0) 7.5 (2.6) 5.3 (2.1) c <0.001
ApoA‐I levels, μg/mL 1.76 (1.3) 1.74 (1.3) 1.74 (1.1) 0.99
CSF PLA2 activity, RFU/min 887 (233) 917 (220) 980 (269) 0.32
CSF acid sphingomyelinase, RFU/min 25 (10) 24 (8) 15 (6)c 0.001
CSF neutral sphingomyelinase, RFU/min 22 (17,26) 19 (17,24) 20 (18,24) 0.38
CSF tau, pg/mL 275 (154) 278 (175) 489 (227)c <0.001
CSF β‐amyloid 42, pg/mL 727 (288) 737 (269) 522 (223)c <0.001

Data presented as mean (SD) or median (25%, 75% percentile) for nonnormally distributed data. Cholesterol efflux capacity of CSF was measured in all samples and normalized to efflux of 5 μg of purified apoE run in every plate. The 3 groups were compared using a linear regression model. The difference in cholesterol efflux capacity persisted after adjusting for CSF lipids or apolipoprotein levels. AD indicates Alzheimer's disease; CH, cognitively healthy; CSF, cerebrospinal fluid; MCI, mild cognitive impairment; PC, phosphatidylcholine; PLA2, phospholipase A2; RFU, relative fluorescence unit; SM, sphingomyelin.

a

CH compared with AD, P<0.001.

b

CH compared with MCI, P<0.001.

c

AD compared with CH and MCI, P<0.001.