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. Author manuscript; available in PMC: 2019 Jun 1.
Published in final edited form as: J Acquir Immune Defic Syndr. 2018 Jun 1;78(2):248–256. doi: 10.1097/QAI.0000000000001666

Table 1.

Demographic and clinical characteristics, and co-morbidities of HIV participants, uninfected volunteers and Alzheimer’s disease group

HIV+ HIV− AD P
N 68 13 24 -
Demographics
Age, years

43 (35; 48)

39 (37.5; 52.5)

76.5(67;79.5)

<0.0001
Education, years 8 (5;11) 12 (10.5;16) 4 (2;6) <0.0001
Gender, n male (%) 33 (49) 10 (77) 8(33) 0.0405
Caucasians, n (%) 66 (97) 13 (100) 22 (92) 0.3688
Clinical
Durationa,b, months 89 (31; 135)a - 36 (24;60)b -
MEEM - - 14(9.5;20) -
MoCA, (n=8) 11.5(10.5;12.5) -
FAQ - - 23.5(15;27.5) -
GDS 0.65 (0.30; 1.05) 0.0(0.0; 0.2) - -
Depression 13 (8, 25)c - 1(0.5;3)d -
Co-morbidities
HCVe, n (%)

12 (18)

0

0

-
Log Plasma HCV RNA 2.9 (1.7; 5.9) 0 0 -

Data are median (IQR) or number of cases (%).Participants co-infected with HCV were not on treatment with interferon-gamma. Clinical duration:

a

of infection on HIV-positive;

b

of symptoms on AD. Cognitive impairment evaluated by: global deficit score (GDS) on HIV-positive; minimental state examination (MMSE); Montreal Cognitive Assessment (MoCA); Functional Activities Questionnaire (Pfeffer’s FAQ) on AD. Major depression disorder (MDD) diagnosed by

c

Beck depression inventory (BDI) on HIV-positive;

d

Geriatric Depression scale (GD scale) on AD.

e

Hepatitis C virus (HCV) status was assessed by antibody testing (Abbott-Architect).