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. 2016 Jun 15;11(6):e0157531. doi: 10.1371/journal.pone.0157531

Table 1. Baseline Characteristics, Patients Who Received Placebo First Compared to Those That Received Pitavastatin First.

Characteristics Placebo(n = 12) Pitavastatin(n = 12)
Age, years* 46.7 (6.8) 49.6 (10.6)
Sex, n (%)
 Male 6 (50) 8 (66.7)
 Female 6 (50) 4 (33.3)
Body mass index, kg/m2* 22.5 (3.4) 23.8 (2.7)
Underlying conditions, n (%)
 No 8 (66.7) 4 (33.3)
 Dyslipidemia 2 (16.7) 4 (33.3)
 Chronic hepatitis B and C virus infection 2 (16.7) 2 (16.7)
 Others 0 (0) 2 (16.7)
Cardiovascular risk factors, n (%)$
 <2 11 (91.7) 7 (58.3)
 ≥2 1 (8.3) 5 (41.7)
Baseline creatinine, mg/dL* 0.9 (0.2) 0.9 (0.2)
Baseline FBS, mg/dL* 97.1 (10.5) 100.8 (10.1)
Baseline CD4 cell counts, cells/mm3* 718.1 (181.2) 641.9 (196.5)
HIV RNA <40 copies/mL, n (%) 11 (91.7) 12 (100)
Duration of ATV/r use, months# 36 (24–36) 42 (30–54)
ARV regimens combined with ATV/r, n (%)
 TDF + FTC/3TC 6 (50) 5 (41.7)
 TDF + other NRTIs (exclude 3TC/FTC) 2 (16.7) 2 (16.7)
 No TDF in backbone 4 (33.3) 5 (41.7)

*Mean (SD),

$current smoking, systolic blood pressure ≥140 mmHg or on antihypertensive drugs, HDL <40 mg/dL, first-degree relative <55 years in male and <65 years in female, and age >45 years in male or >55 years in female,

#median (IQR)

3TC: lamivudine, ARV: antiretroviral, ATV/r: atazanavir/ritonavir, FBS: fasting blood sugar, FTC: emtricitabine, IQR: interquartile range, SD: standard deviation, TDF: tenofovir disoproxil fumarate.